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        <title>Angewandte Chemie via MedWorm.com</title>
        <description>MedWorm.com provides a medical RSS filtering service. Over 6000 RSS medical sources are combined and output via different filters. This feed contains the latest items from the 'Angewandte Chemie' source.</description>
        <link><![CDATA[http://www.medworm.com/rss/search.php?qu=Angewandte+Chemie&t=Angewandte+Chemie&s=Search&f=source]]></link>
        <lastBuildDate>Thu, 09 Feb 2012 13:01:27 +0100</lastBuildDate>
        <item>
            <title>&quot;Angew Chem Int Ed Engl&quot;[ta]; +126 new citations</title>
            <link>http://www.medworm.com/index.php?rid=5654413&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fsites%2Fentrez%3Fcmd%3DSearch%26db%3Dpubmed%26term%3D%28%2520%28%2522Angew%2520Chem%2520Int%2520Ed%2520Engl%2522%255Bta%255D%29%2520AND%2520%25222012%252F01%252F22%252010.30%2522%255BEDAT%255D%253A%25222012%252F02%252F03%252007.36%2522%255BEDAT%255D%29</link>
            <description>126 new pubmed citations were retrieved for your search.
Click on the search hyperlink below to display the complete search results:

&quot;Angew Chem Int Ed Engl&quot;[ta]
These pubmed results were generated on 2012/02/03PubMed, a service of the National Library of Medicine, includes over 15 million 
citations for biomedical articles back to the 1950's.
These citations are from MEDLINE and additional life science journals. 
PubMed includes links to many sites providing full text articles and other related resources. (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5654413</comments>
            <pubDate>Fri, 03 Feb 2012 12:36:02 +0100</pubDate>
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        <item>
            <title>&quot;Angew Chem Int Ed Engl&quot;[ta]; +116 new citations</title>
            <link>http://www.medworm.com/index.php?rid=5618347&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fsites%2Fentrez%3Fcmd%3DSearch%26db%3Dpubmed%26term%3D%28%2520%28%2522Angew%2520Chem%2520Int%2520Ed%2520Engl%2522%255Bta%255D%29%2520AND%2520%25222012%252F01%252F09%252014.18%2522%255BEDAT%255D%253A%25222012%252F01%252F22%252010.30%2522%255BEDAT%255D%29</link>
            <description>116 new pubmed citations were retrieved for your search.
Click on the search hyperlink below to display the complete search results:

&quot;Angew Chem Int Ed Engl&quot;[ta]
These pubmed results were generated on 2012/01/22PubMed, a service of the National Library of Medicine, includes over 15 million 
citations for biomedical articles back to the 1950's.
These citations are from MEDLINE and additional life science journals. 
PubMed includes links to many sites providing full text articles and other related resources. (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5618347</comments>
            <pubDate>Sun, 22 Jan 2012 15:30:01 +0100</pubDate>
            <guid isPermaLink="false">5618347</guid>        </item>
        <item>
            <title>Enantioselective Synthesis of Spiro Cyclopentane-1,3'-indoles and 2,3,4,9-Tetrahydro-1H-carbazoles by Iridium-Catalyzed Allylic Dearomatization and Stereospecific Migration.</title>
            <link>http://www.medworm.com/index.php?rid=5575758&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22223488%26dopt%3DAbstract</link>
            <description>Authors: Wu QF, Zheng C, You SL
    Abstract
    Rings with a twist: The highly enantioselective construction of five-membered spiroindolenines has been realized by the iridium-catalyzed intramolecular allylic dearomatization of indoles. The stereospecific migration of these spiro cyclopentane-1,3'-indole products provides enantioenriched 2,3,4,9-tetrahydro-1H-carbazoles.
    PMID: 22223488 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575758</comments>
            <pubDate>Thu, 05 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5575758</guid>        </item>
        <item>
            <title>Fine-tuning the π-π Aromatic Interactions in Peptides: Somatostatin Analogues Containing Mesityl Alanine.</title>
            <link>http://www.medworm.com/index.php?rid=5575754&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22223594%26dopt%3DAbstract</link>
            <description>Authors: Martín-Gago P, Gomez-Caminals M, Ramón R, Verdaguer X, Martin-Malpartida P, Aragón E, Fernández-Carneado J, Ponsati B, López-Ruiz P, Cortes MA, Colás B, Macias MJ, Riera A
    Abstract
    The π-π aromatic interactions between amino acids 6, 7, and 11 in the natural hormone somatostatin are crucial for conformational stability. In their Communication (DOI: 10.1002/anie.201106406), M. J. Macias, A. Riera, and co-workers describe that peptidic analogues obtained by replacing each phenylalanine with mesitylalanine are conformationally more rigid than the parent hormone. This strategy has yielded the first 3D structures of 14-amino-acid somatostatin analogues.
    PMID: 22223594 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575754</comments>
            <pubDate>Thu, 05 Jan 2012 05:00:00 +0100</pubDate>
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        <item>
            <title>A Highly Selective Ethylene Tetramerization Catalyst.</title>
            <link>http://www.medworm.com/index.php?rid=5575768&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22223188%26dopt%3DAbstract</link>
            <description>Authors: Shaikh Y, Albahily K, Sutcliffe M, Fomitcheva V, Gambarotta S, Korobkov I, Duchateau R
    Abstract
    Small change, big difference: The introduction of an additional CH(2) group into the bridge of ligands with two P/N units leads to a different selectivity of the according chromium-based catalysts. While 1 produces an ethylene trimerization system, 2 provides an unprecedented ethylene tetramerization system that produces 1-octene with high purity and little or no polymer side products (see scheme; DMAO=Me(3) Al-depleted methylaluminoxane).
    PMID: 22223188 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575768</comments>
            <pubDate>Tue, 03 Jan 2012 05:00:00 +0100</pubDate>
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        <item>
            <title>A Self-Powered &quot;Sense-Act-Treat&quot; System that is Based on a Biofuel Cell and Controlled by Boolean Logic.</title>
            <link>http://www.medworm.com/index.php?rid=5575764&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22223361%26dopt%3DAbstract</link>
            <description>A Self-Powered &quot;Sense-Act-Treat&quot; System that is Based on a Biofuel Cell and Controlled by Boolean Logic.
    Angew Chem Int Ed Engl. 2012 Jan 3;
    Authors: Zhou M, Zhou N, Kuralay F, Windmiller JR, Parkhomovsky S, Valdés-Ramírez G, Katz E, Wang J
    Abstract
    Bio-logic-al: An autonomous, integrated &quot;sense-act-treat&quot; system that is based on an enzymatic biofuel cell has been developed. The system couples a biocomputing logic-detection method with a drug-release system to provide a logic-activated therapeutic intervention in response to a simulated abnormal physiological state, without the need for an external power source, control electronics, or microelectromechanical actuators.
    PMID: 22223361 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575764</comments>
            <pubDate>Tue, 03 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5575764</guid>        </item>
        <item>
            <title>Lattice Expansion of Highly Oriented 2D Phthalocyanine Covalent Organic Framework Films.</title>
            <link>http://www.medworm.com/index.php?rid=5575763&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22223402%26dopt%3DAbstract</link>
            <description>Authors: Spitler EL, Colson JW, Uribe-Romo FJ, Woll AR, Giovino MR, Saldivar A, Dichtel WR
    Abstract
    Expanding into application: Covalent organic framework (COF) films are ideally suited for vertical charge transport and serve as precursors of ordered heterojunctions. Their pores, however, were previously too small to accommodate continuous networks of complementary electron acceptors. Four phthalocyanine COFs with increased pore size well into the mesoporous regime are now described (see example).
    PMID: 22223402 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575763</comments>
            <pubDate>Tue, 03 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5575763</guid>        </item>
        <item>
            <title>Oxygen-Mediated Coupling of Alcohols over Nanoporous Gold Catalysts at Ambient Pressures.</title>
            <link>http://www.medworm.com/index.php?rid=5575762&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22223430%26dopt%3DAbstract</link>
            <description>Authors: Kosuda KM, Wittstock A, Friend CM, Bäumer M
    Abstract
    Unsupported catalyst for green chemistry: The aerobic oxidation and coupling of primary alcohols (methanol, ethanol, n-butanol) to give the corresponding aldehydes and esters at temperatures below 100 °C is facilitated by unsupported nanoporous gold catalysts. The experimental conditions employed allow a close comparison to model experiments and open the door to a molecular-level understanding of the reaction.
    PMID: 22223430 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575762</comments>
            <pubDate>Tue, 03 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5575762</guid>        </item>
        <item>
            <title>Design Rules: A Net and Archimedean Polyhedra Score Big for Self-Assembly.</title>
            <link>http://www.medworm.com/index.php?rid=5575819&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22213105%26dopt%3DAbstract</link>
            <description>Authors: Macgillivray LR
    Abstract
    Caged: Taking its origin in recent work by Ward and co-workers, an overview is given over the synthesis of Archimedean and Platonic bodies by different approaches such as hydrogen-bonded self-assembly and coordination chemistry.
    PMID: 22213105 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575819</comments>
            <pubDate>Mon, 02 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5575819</guid>        </item>
        <item>
            <title>Abstracts.</title>
            <link>http://www.medworm.com/index.php?rid=5575803&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22213351%26dopt%3DAbstract</link>
            <description>Authors: 
    PMID: 22213351 [PubMed - in process] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575803</comments>
            <pubDate>Mon, 02 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5575803</guid>        </item>
        <item>
            <title>50 years ago ...</title>
            <link>http://www.medworm.com/index.php?rid=5575802&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22213352%26dopt%3DAbstract</link>
            <description>Authors: 
    PMID: 22213352 [PubMed - in process] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575802</comments>
            <pubDate>Mon, 02 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5575802</guid>        </item>
        <item>
            <title>Preview: angew. Chem. Int. Ed. 2/2012.</title>
            <link>http://www.medworm.com/index.php?rid=5575801&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22213353%26dopt%3DAbstract</link>
            <description>Authors: 
    PMID: 22213353 [PubMed - in process] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575801</comments>
            <pubDate>Mon, 02 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5575801</guid>        </item>
        <item>
            <title>Photoinduced Memory Effect in a Redox Controllable Bistable Mechanical Molecular Switch.</title>
            <link>http://www.medworm.com/index.php?rid=5575800&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22213358%26dopt%3DAbstract</link>
            <description>Authors: Avellini T, Li H, Coskun A, Barin G, Trabolsi A, Basuray AN, Dey SK, Credi A, Silvi S, Stoddart JF, Venturi M
    Abstract
    Something to remember: A rotaxane could be operated as a bistable memory element under kinetic control. Data is be written on the molecule by an oxidation stimulus and locked by UV light irradiation. After the writing session, the oxidized species is reduced back to the original form without losing the written data for a few hours. Light irradiation also protects nonoxidized rotaxanes from accidental writing.
    PMID: 22213358 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575800</comments>
            <pubDate>Mon, 02 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5575800</guid>        </item>
        <item>
            <title>Multiplex Imaging of an Intracellular Proteolytic Cascade by using a Broad-Spectrum Nanoquencher.</title>
            <link>http://www.medworm.com/index.php?rid=5575795&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22213412%26dopt%3DAbstract</link>
            <description>Authors: Huang X, Swierczewska M, Choi KY, Zhu L, Bhirde A, Park J, Kim K, Xie J, Niu G, Lee KC, Lee S, Chen X
    Abstract
    Turn off the lights! A universal nanoquencher that quenches a broad range of visible to near-infrared dyes by using a series of dark quenchers incorporated into a cell-permeable mesoporous silica nanoparticle has been developed. In combination with dye-labeled substrates, this nanoquencher boosts multiple fluorescence signals upon specific proteolysis, which allows real-time imaging of proteolytic cascades.
    PMID: 22213412 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575795</comments>
            <pubDate>Mon, 02 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5575795</guid>        </item>
        <item>
            <title>Origin of Low CO(2)  Selectivity on Platinum in the Direct Ethanol Fuel Cell.</title>
            <link>http://www.medworm.com/index.php?rid=5575785&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22213572%26dopt%3DAbstract</link>
            <description>Origin of Low CO(2) Selectivity on Platinum in the Direct Ethanol Fuel Cell.
    Angew Chem Int Ed Engl. 2012 Jan 2;
    Authors: Kavanagh R, Cao XM, Lin WF, Hardacre C, Hu P
    Abstract
    Calculated answer: First-principles calculations are applied to calculate the energy barrier for the key step in CO formation on a Pt surface (see picture, Pt blue, Pt atoms on step edge yellow) to understand the low CO(2) selectivity in the direct ethanol fuel cell. The presence of surface oxidant species such as O (brown bar) and OH (red bar) leads to an increase of the engergy barrier and thus an inhibition of the key step.
    PMID: 22213572 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575785</comments>
            <pubDate>Mon, 02 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5575785</guid>        </item>
        <item>
            <title>Catalytic Polymerization of Anthracene in a Recyclable SBA-15 Reactor with High Iron Content by a Friedel-Crafts Alkylation.</title>
            <link>http://www.medworm.com/index.php?rid=5575783&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22213589%26dopt%3DAbstract</link>
            <description>Authors: Kim J, Anand C, Talapaneni SN, You J, Aldeyab SS, Kim E, Vinu A
    Abstract
    Ironing it out: A FeSBA-15 catalyst with a high iron content as well as a large pore diameter has been synthesized and used for the production of soluble poly(methylene anthracene) (PMAn, see scheme). The catalyst is stable, active, reusable, and affords a high yield of high molecular weight PMAn. The properties of the PMAns obtained can be controlled by tuning the specific surface area, pore diameter, pore volume, and Fe content of the catalysts.
    PMID: 22213589 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575783</comments>
            <pubDate>Mon, 02 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5575783</guid>        </item>
        <item>
            <title>Transamidation of Primary Amides with Amines Using Hydroxylamine Hydrochloride as an Inorganic Catalyst.</title>
            <link>http://www.medworm.com/index.php?rid=5575817&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22213128%26dopt%3DAbstract</link>
            <description>Authors: Allen CL, Atkinson BN, Williams JM
    Abstract
    Metal-free catalysis: A novel method for the transamidation of primary amides with primary or secondary amines provides access to secondary and tertiary amides, utilizing catalytic quantities of hydroxylamine hydrochloride to activate the chemically robust primary amide group. A mechanism of primary amide activation through a hydrogen-bonding complex is proposed.
    PMID: 22213128 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575817</comments>
            <pubDate>Fri, 30 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5575817</guid>        </item>
        <item>
            <title>Reversibly Switching the Function of a Surface between Attacking and Defending against Bacteria.</title>
            <link>http://www.medworm.com/index.php?rid=5575814&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22213162%26dopt%3DAbstract</link>
            <description>Authors: Cao Z, Mi L, Mendiola J, Ella-Menye JR, Zhang L, Xue H, Jiang S
    Abstract
    Attack or defend! A smart polymer surface has two reversibly switchable equilibrium states, a cationic N,N-dimethyl-2-morpholinone (CB-Ring) and a zwitterionic carboxy betaine (CB-OH). CB-Ring will kill bacteria upon contact under dry conditions, whereas CB-OH will release the previously attached and dead bacteria and further resist adhesion of bacteria under wet conditions.
    PMID: 22213162 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575814</comments>
            <pubDate>Fri, 30 Dec 2011 05:00:00 +0100</pubDate>
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        <item>
            <title>Selenenylsulfide-linked Homogeneous Glycopeptides and Glycoproteins: Synthesis of Human &quot;Hepatic Se Metabolite A&quot;</title>
            <link>http://www.medworm.com/index.php?rid=5575806&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22213253%26dopt%3DAbstract</link>
            <description>Selenenylsulfide-linked Homogeneous Glycopeptides and Glycoproteins: Synthesis of Human &quot;Hepatic Se Metabolite A&quot;
    Angew Chem Int Ed Engl. 2011 Dec 30;
    Authors: Boutureira O, Bernardes GJ, Fernández-González M, Anthony DC, Davis BG
    Abstract
    Introducing selenium: The synthesis and full characterization of human hepatic Se metabolite A has been accomplished by using a robust, efficient, and Cys-specific selenenylation protocol (see scheme; NaPi=sodium phosphate). The selenenylsulfide linkage is sufficiently stable to allow quantification of Se-containing glycoconjugates in biological fluids by using atomic detection methods.
    PMID: 22213253 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575806</comments>
            <pubDate>Fri, 30 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5575806</guid>        </item>
        <item>
            <title>Nonlinear Enhancement of Chiroptical Response through Subcomponent Substitution in M(4) L(6)  Cages.</title>
            <link>http://www.medworm.com/index.php?rid=5575805&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22213279%26dopt%3DAbstract</link>
            <description>Nonlinear Enhancement of Chiroptical Response through Subcomponent Substitution in M(4) L(6) Cages.
    Angew Chem Int Ed Engl. 2011 Dec 30;
    Authors: Ousaka N, Clegg JK, Nitschke JR
    Abstract
    One for all, all for one: A self-assembled M(4) L(6) cage, incorporating small amounts of enantiopure subcomponents at the peripheries, forms predominantly with a one-handed twist at all metal centers. Strong stereochemical coupling between metal centers in the cage amplifies energy differences between the ΔΔΔΔ and ΛΛΛΛ diastereomers as compared to analogous mononuclear metal complexes (see picture; red and gray bars denote chiral and achiral subcomponents, respectively).
    PMID: 22213279 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575805</comments>
            <pubDate>Fri, 30 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5575805</guid>        </item>
        <item>
            <title>Calixarene-Based Nanoscale Coordination Cages.</title>
            <link>http://www.medworm.com/index.php?rid=5575799&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22213359%26dopt%3DAbstract</link>
            <description>Authors: Liu M, Liao W, Hu C, Du S, Zhang H
    Abstract
    Molecular shuttlecocks: The introduction of tripodal ternary acids to the cobalt/calixarene (green) systems leads to the formation of four unprecedented calixarene-based nanoscale coordination cages through a [6+8] condensation. The overall periphery diameters of the nanocages range from 3.3 to 4.7 nm, and there are two sizes for the internal cavities (1.1 and 1.7 nm).
    PMID: 22213359 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575799</comments>
            <pubDate>Fri, 30 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5575799</guid>        </item>
        <item>
            <title>Nucleic Acid and Peptide Aptamers: Fundamentals and Bioanalytical Aspects.</title>
            <link>http://www.medworm.com/index.php?rid=5575798&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22213382%26dopt%3DAbstract</link>
            <description>Authors: Mascini M, Palchetti I, Tombelli S
    Abstract
    In recent years new nucleic acid and protein-based combinatorial molecules have attracted the attention of researchers working in various areas of science, ranging from medicine to analytical chemistry. These molecules, called aptamers, have been proposed as alternatives to antibodies in many different applications. The aim of this Review is to illustrate the peculiarities of these combinatorial molecules which have initially been explored for their importance in molecular medicine, but have enormous potential in other biotechnological fields historically dominated by antibodies, such as bioassays. A description of these molecules is given, and the methods for their selection and production are also summarized. Moreover, critical...</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575798</comments>
            <pubDate>Fri, 30 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5575798</guid>        </item>
        <item>
            <title>Templated Dynamic Synthesis of a [3]Catenane.</title>
            <link>http://www.medworm.com/index.php?rid=5575794&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22213430%26dopt%3DAbstract</link>
            <description>Authors: Cougnon FB, Jenkins NA, Pantoş GD, Sanders JK
    Abstract
    Three rings: The self-assembly of a water-soluble [3]catenane from a library composed of two linear building blocks, both terminated by cysteine components, is promoted either by a high salt concentration or by the presence of spermine. The spermine-templated synthesis of the [3]catenane shows that such structures can exhibit strong binding interactions with a biologically relevant target in water under near-physiological conditions.
    PMID: 22213430 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575794</comments>
            <pubDate>Fri, 30 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5575794</guid>        </item>
        <item>
            <title>Design, Total Chemical Synthesis, and X-Ray Structure of a Protein Having a Novel Linear-Loop Polypeptide Chain Topology.</title>
            <link>http://www.medworm.com/index.php?rid=5575793&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22213444%26dopt%3DAbstract</link>
            <description>Authors: Mandal K, Pentelute BL, Bang D, Gates ZP, Torbeev VY, Kent SB
    Abstract
    Lassoed at the other end: Original synthetic and structure determination methods were used to make a protein molecule with an unprecedented linear-loop polypeptide chain topology, and to characterize its X-ray structure.
    PMID: 22213444 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575793</comments>
            <pubDate>Fri, 30 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5575793</guid>        </item>
        <item>
            <title>Reversible Insertion of 1,3-Di-tert-butylimidazol-2-ylidene into a RuH Bond and Bimetallic Activation of a NC Bond of Imidazoline.</title>
            <link>http://www.medworm.com/index.php?rid=5575791&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22213483%26dopt%3DAbstract</link>
            <description>Authors: Kaiho A, Suzuki H
    Abstract
    Reversible insertion of NHC: 1,3-Di-tert-butylimidazol-2-ylidene was inserted into a ruthenium-hydride bond of [Cp*Ru(μ-H)(4) RuCp*] to form a 4-imidazoline complex that underwent a dynamic process, namely 1,3-migratory pendulum motion of the 4-imidazoline ligand. Bimetallic-system-assisted NC bond cleavage of the imidazoline ligand proceeded to generate a pseudo-diazaruthenacycle.
    PMID: 22213483 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575791</comments>
            <pubDate>Fri, 30 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5575791</guid>        </item>
        <item>
            <title>An Accurate Pharmacophore Mapping Method by NMR Spectroscopy.</title>
            <link>http://www.medworm.com/index.php?rid=5575787&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22213544%26dopt%3DAbstract</link>
            <description>Authors: Mizukoshi Y, Abe A, Takizawa T, Hanzawa H, Fukunishi Y, Shimada I, Takahashi H
    Abstract
    Irradiation makes the difference: The relaxation-rate differences of individual ligand protons (H(A) , H(B) ) between the experiment with and that without (blue) saturation of the protons of the protein target reflect the proximity to the protein surface. Thus the binding portions of ligand molecules could be identified using this &quot;difference of inversion recovery rate with and without target irradiation&quot; (DIRECTION) methodology.
    PMID: 22213544 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575787</comments>
            <pubDate>Fri, 30 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5575787</guid>        </item>
        <item>
            <title>Hydrogen Production Coupled to Hydrocarbon Oxygenation from Photocatalytic Water Splitting.</title>
            <link>http://www.medworm.com/index.php?rid=5575781&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22213598%26dopt%3DAbstract</link>
            <description>Authors: Singh WM, Pegram D, Duan H, Kalita D, Simone P, Emmert GL, Zhao X
    Abstract
    The evolution of H(2) and the oxygenation of hydrocarbons from photocatalytic water splitting are reported. In their Communication (DOI: 10.1002/anie.201106494), X. Zhao et al. develop a homogeneous system for simultaneous H(2) production and hydrocarbon oxidation, in which water is the source of both O(2) and H(2) . Two photosensitizers make possible the coupling of the hydrocarbon oxygenation reaction to the H(2) production process. (Photo courtesy of Rachel Wang.).
    PMID: 22213598 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575781</comments>
            <pubDate>Fri, 30 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5575781</guid>        </item>
        <item>
            <title>Monitoring of Liquid-Phase Organic Reactions by Photoelectron Spectroscopy.</title>
            <link>http://www.medworm.com/index.php?rid=5575775&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22213634%26dopt%3DAbstract</link>
            <description>Authors: Kolbeck C, Niedermaier I, Taccardi N, Schulz PS, Maier F, Wasserscheid P, Steinrück HP
    Abstract
    Nucleophilic substitution belongs to the fundamental organic reaction mechanisms since the pioneering work of C. K. Ingold in the 1920s. In their Communication (DOI: 10.1002/anie.201107402), H.-P. Steinrück and co-workers monitor the alkylation of a tertiary amine attached to an imidazolium cation with a chloroalkylsulfonate anion by photoelectron spectroscopy, which can distinguish between convalently bound chlorine (Cl(cov) ) and chloride (Cl(ion) ).
    PMID: 22213634 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575775</comments>
            <pubDate>Fri, 30 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5575775</guid>        </item>
        <item>
            <title>Controlling the Nucleation and Growth of Silver on Palladium Nanocubes by Manipulating the Reaction Kinetics.</title>
            <link>http://www.medworm.com/index.php?rid=5575772&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22213644%26dopt%3DAbstract</link>
            <description>Authors: Zeng J, Zhu C, Tao J, Jin M, Zhang H, Li ZY, Zhu Y, Xia Y
    Abstract
    Feeding your face. In their Communication (10.1002/anie. 201107061), Y. Xia and co-workers show that it is possible to shape-selectively grow bimetallic palladium-silver nanocrystals. By limiting the supply of silver atoms (red) nucleation and growth occurs on only one, or a few, of the six equivalent faces of a cubic palladium seed, as represented by the presence of hungry and feeding frogs.
    PMID: 22213644 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575772</comments>
            <pubDate>Fri, 30 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5575772</guid>        </item>
        <item>
            <title>A High-Performance Ytterbium-Based Nanoparticulate Contrast Agent for In Vivo X-Ray Computed Tomography Imaging.</title>
            <link>http://www.medworm.com/index.php?rid=5575765&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22223303%26dopt%3DAbstract</link>
            <description>Authors: Liu Y, Ai K, Liu J, Yuan Q, He Y, Lu L
    Abstract
    Enlightening particles: A novel contrast agent for in vivo X-ray computed tomography (CT) imaging is composed of an Yb-based nanoparticle (NP) that is stabilized with oleic acid and modified with the biocompatible polymer DSPE-PEG 2000. The contrast agent exhibits long circulation time in vivo and low toxicity and is also much more effective than a clinical iodinated agent.
    PMID: 22223303 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575765</comments>
            <pubDate>Fri, 30 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5575765</guid>        </item>
        <item>
            <title>In Vitro Developmental Acceleration of Hippocampal Neurons on Nanostructures of Self-Assembled Silica Beads in Filopodium-Size Ranges.</title>
            <link>http://www.medworm.com/index.php?rid=5575756&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22223541%26dopt%3DAbstract</link>
            <description>Authors: Kang K, Choi SE, Jang HS, Cho WK, Nam Y, Choi IS, Lee JS
    Abstract
    Topographical cues play an important role in in vitro neuronal development. In their Communication (DOI: 10.1002/anie.201106271), Y. Nam, I. S. Choi, J. S. Lee, and co-workers show that neuritogenetic acceleration occurs on silica-bead monolayers made up of beads with a diameter of more than 200 nm, but not on monolayers of beads with smaller diameters. The biochemical study indicates neurons sense topographical differences in nanostructures and alter their behavior accordingly.
    PMID: 22223541 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575756</comments>
            <pubDate>Fri, 30 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5575756</guid>        </item>
        <item>
            <title>---</title>
            <link>http://www.medworm.com/index.php?rid=5575755&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22223565%26dopt%3DAbstract</link>
            <description>Angew Chem Int Ed Engl. 2011 Dec 30;
    Authors: Upert G, Bouillère F, Wennemers H
    Abstract
    Functionalized oligoproline scaffolds that have defined lengths have been shown to control the size of silver nanoparticles that are formed in the Tollens reaction. In their Communication (DOI: 10.1002/anie.201107183), H. Wennemers and co-workers demonstrate the correlation between the molecular dimensions of the peptide scaffold and the size of the nanoparticles that are produced in an approach that opens the door to precise control of the size of metal nanoparticles.
    PMID: 22223565 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575755</comments>
            <pubDate>Fri, 30 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5575755</guid>        </item>
        <item>
            <title>Ribose Found in the Gas Phase.</title>
            <link>http://www.medworm.com/index.php?rid=5575789&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22213535%26dopt%3DAbstract</link>
            <description>Authors: Cocinero EJ, Lesarri A, Ecija P, Basterretxea FJ, Grabow JU, Fernández JA, Castaño F
    Abstract
    Sweet truth: The search for sugars in interstellar space is hampered by a lack of spectroscopic information. D-Ribose is now the first C(5) sugar observed in the gas phase using microwave spectroscopy. The rotational spectrum revealed six conformations of free ribose, adopting preferentially β-pyranose rings and higher-energy α-pyranose forms. No evidence of α-/β-furanoses or linear forms was found, unlike biological systems, where β-furanoses are found in RNA.
    PMID: 22213535 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575789</comments>
            <pubDate>Wed, 28 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5575789</guid>        </item>
        <item>
            <title>Unveiling the Shape of Aspirin in the Gas Phase.</title>
            <link>http://www.medworm.com/index.php?rid=5575766&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22223259%26dopt%3DAbstract</link>
            <description>Authors: Cabezas C, Alonso JL, López JC, Mata S
    Abstract
    Accurate structural information: The first high-resolution study of isolated gas-phase acetyl salicylic acid (aspirin) is reported. Solid aspirin was vaporized by laser ablation, expanded in a supersonic jet, and characterized by Fourier transform microwave spectroscopy. Two different neutral structures have been identified from the analysis of the rotational spectrum.
    PMID: 22223259 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575766</comments>
            <pubDate>Wed, 28 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5575766</guid>        </item>
        <item>
            <title>Brønsted Acid-Catalyzed Asymmetric Propargylation of Aldehydes.</title>
            <link>http://www.medworm.com/index.php?rid=5575759&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22223476%26dopt%3DAbstract</link>
            <description>Authors: Jain P, Wang H, Houk KN, Antilla JC
    Abstract
    Which gets activated? A versatile and highly enantioselective chiral Brønsted acid-catalyzed method for the propargylation of aldehydes is described to provide a range of chiral homopropargylic alcohols. Computational studies support the belief that the chiral phosphoric acid activates the allenyl boronic acid pinacol ester reagent rather than the aldehyde.
    PMID: 22223476 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575759</comments>
            <pubDate>Wed, 28 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5575759</guid>        </item>
        <item>
            <title>Chlorostyrenes in Iron-Catalyzed Biaryl Coupling Reactions.</title>
            <link>http://www.medworm.com/index.php?rid=5575820&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22213100%26dopt%3DAbstract</link>
            <description>Authors: Gülak S, Jacobi von Wangelin A
    Abstract
    An effective protocol for iron-catalyzed biaryl syntheses by coupling chlorostyrenes with aryl Grignard reagents requires only mild reaction conditions and tolerates various functional groups. The underlying activation of deactivated aryl chlorides proceeds through a rate-determining coordination of the catalyst to the vinyl substituent and subsequent haptotropic migration along the conjugated π system to the site of CCl bond cleavage.
    PMID: 22213100 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575820</comments>
            <pubDate>Tue, 27 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5575820</guid>        </item>
        <item>
            <title>Production of Renewable Aromatic Compounds by Catalytic Fast Pyrolysis of Lignocellulosic Biomass with Bifunctional Ga/ZSM-5 Catalysts.</title>
            <link>http://www.medworm.com/index.php?rid=5575809&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22213226%26dopt%3DAbstract</link>
            <description>Authors: Cheng YT, Jae J, Shi J, Fan W, Huber GW
    Abstract
    Burn, baby, burn! A new bifunctional catalyst (Ga/ZSM-5) displays increased selectivity for the production of aromatic compounds during the catalytic fast pyrolysis of biomass. With this Ga-promoted ZSM-5 catalyst, olefins such as ethylene and propylene, which are produced as intermediates, are more efficiently converted into aromatics, especially benzene. Ga/ZSM-5 also promotes decarbonylation and olefin-aromatization reactions.
    PMID: 22213226 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575809</comments>
            <pubDate>Tue, 27 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5575809</guid>        </item>
        <item>
            <title>Large-Scale, Low-Cost Fabrication of Janus-Type Emulsifiers by Selective Decoration of Natural Kaolinite Platelets.</title>
            <link>http://www.medworm.com/index.php?rid=5575804&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22213281%26dopt%3DAbstract</link>
            <description>Authors: Hirsemann D, Shylesh S, De Souza RA, Diar-Bakerly B, Biersack B, Mueller DN, Martin M, Schobert R, Breu J
    Abstract
    Kaolinite platelets have inherent Janus character owing to a polar crystal structure. This character is, however, ineffective without selective modification of the two hydrophilic external basal surfaces. Amplification of the difference in chemical nature of the surfaces is achieved by cation exchange on one side and by covalent grafting on the other. After adjustment of the surface tension, kaolinite is an effective emulsifier.
    PMID: 22213281 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575804</comments>
            <pubDate>Tue, 27 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5575804</guid>        </item>
        <item>
            <title>The Mechanism of OO Bond Formation in Tanaka's Water Oxidation Catalyst.</title>
            <link>http://www.medworm.com/index.php?rid=5575818&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22213120%26dopt%3DAbstract</link>
            <description>Authors: Ghosh S, Baik MH
    Abstract
    Oh-oh! The mechanism of water oxidation by Tanaka's catalyst (shown schematically in the picture) is studied using quantum chemical methods. The formation of the OO bond between the two terminal oxo moieties of the catalyst lacks any thermodynamic driving force. The redox-active quinone ligand, however, assists in the addition of a water molecule to one of the Ru centers, thus facilitating the release of dioxygen.
    PMID: 22213120 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575818</comments>
            <pubDate>Fri, 23 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5575818</guid>        </item>
        <item>
            <title>Isolation and Total Synthesis of Icumazoles and Noricumazoles-Antifungal Antibiotics and Cation-Channel Blockers from Sorangium cellulosum.</title>
            <link>http://www.medworm.com/index.php?rid=5575816&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22213143%26dopt%3DAbstract</link>
            <description>Authors: Barbier J, Jansen R, Irschik H, Benson S, Gerth K, Böhlendorf B, Höfle G, Reichenbach H, Wegner J, Zeilinger C, Kirschning A, Müller R
    Abstract
    Joint efforts: The antifungal icumazole A, the potassium-ion-channel inhibitor noricumazole A, and their glycosylated derivatives are new, structurally related secondary metabolites isolated from Sorangium cellulosum. Their structures have been fully assigned by a joint strategy that relied on spectroscopy, derivatization, fragmentation, and finally the first total synthesis of noricumazole A.
    PMID: 22213143 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575816</comments>
            <pubDate>Fri, 23 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5575816</guid>        </item>
        <item>
            <title>Stereoarrays with an All-Carbon Quaternary Center: Diastereoselective Desymmetrization of Prochiral Malonaldehydes.</title>
            <link>http://www.medworm.com/index.php?rid=5575815&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22213150%26dopt%3DAbstract</link>
            <description>Authors: Linclau B, Cini E, Oakes CS, Josse S, Light M, Ironmonger V
    Abstract
    Tamed by chelation: The MgBr(2) chelation of prochiral malonaldehydes allows diastereoselective monoaddition reactions with allyl stannane nucleophiles (see scheme; PG=protecting group, TBDMS=tert-butyldiphenylmethylsilyl, Tr=trityl). In the same pot, addition of a second nucleophile proceeds in high diastereoselectivity to generate nonsymmetric products with up to five contiguous stereogenic centers, including a chiral all-carbon quaternary center.
    PMID: 22213150 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575815</comments>
            <pubDate>Fri, 23 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5575815</guid>        </item>
        <item>
            <title>A Single Water Molecule Trapped Inside Hydrophobic C(60).</title>
            <link>http://www.medworm.com/index.php?rid=5575813&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22213177%26dopt%3DAbstract</link>
            <description>Authors: Thilgen C
    Abstract
    Dry water in a wet dungeon? An isolated H(2) O molecule has been trapped permanently inside hydrophobic C(60) (see picture; green C, white H, red O). The endohedral fullerene H(2) O@C(60) was synthesized by opening, filling, and reclosing the carbon cage. The incarcerated water does not alter the structure of the cage, but it confers an appreciable dipole moment to the new entity with its intrinsically apolar carbon sphere.
    PMID: 22213177 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575813</comments>
            <pubDate>Fri, 23 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5575813</guid>        </item>
        <item>
            <title>Fine-Tuning Conformational Motion of a Self-Assembled Metal-Organic Macrocycle by Multiple CH⋅⋅⋅Anion Hydrogen Bonds.</title>
            <link>http://www.medworm.com/index.php?rid=5575812&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22213186%26dopt%3DAbstract</link>
            <description>Authors: Xie TZ, Guo C, Yu SY, Pan YJ
    Abstract
    Anion switches: A bistable self-assembled metal-organic macrocycle undergoes intramolecular conformational motion that is switched reversibly with anions by multiple hydrogen bonding interactions (see picture; Pd orange, N blue, O red). The molecular bowl fixed with nitrate anion could be freed to a partial chair by adding a tetraphenylborate anion.
    PMID: 22213186 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575812</comments>
            <pubDate>Fri, 23 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5575812</guid>        </item>
        <item>
            <title>Distinguishing DNA by Analog-to-Digital-like Conversion by Using Optofluidic Lasers.</title>
            <link>http://www.medworm.com/index.php?rid=5575811&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22213205%26dopt%3DAbstract</link>
            <description>Authors: Sun Y, Fan X
    Abstract
    Laser precision: A highly sensitive technique based on laser emission for differentiating a target DNA strand from strands that contain single base mismatches has been developed. Laser emission is used to amplify the small difference in signals that are generated by the different strands after hybridization with a molecular beacon (MB, see picture) in a conversion that is similar to analog-to-digital.
    PMID: 22213205 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575811</comments>
            <pubDate>Fri, 23 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5575811</guid>        </item>
        <item>
            <title>Direct Preparation of Sulfide Semiconductor Nanoparticles from the Corresponding Bulk Powders in an Ionic Liquid.</title>
            <link>http://www.medworm.com/index.php?rid=5575810&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22213206%26dopt%3DAbstract</link>
            <description>Authors: Rodríguez-Cabo B, Rodil E, Rodríguez H, Soto A, Arce A
    Abstract
    Just add liquid and stir: Dispersions of metal sulfide nanoparticles (CdS, ZnS, PbS, and MnS) can be prepared directly by mixing the corresponding bulk solid with an appropriate ionic liquid, without further additives or solvents. The selection of the ionic liquid is critical for the viability of this nanoparticle preparation method.
    PMID: 22213206 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575810</comments>
            <pubDate>Fri, 23 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5575810</guid>        </item>
        <item>
            <title>Integrated Laser and Electron Microscopy Correlates Structure of Fluid Catalytic Cracking Particles to Brønsted Acidity.</title>
            <link>http://www.medworm.com/index.php?rid=5575808&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22213229%26dopt%3DAbstract</link>
            <description>Authors: Karreman MA, Buurmans IL, Geus JW, Agronskaia AV, Ruiz-Martínez J, Gerritsen HC, Weckhuysen BM
    Abstract
    Cracking the crackers: Integrated laser and electron microscopy was applied to study individual fluid catalytic cracking catalyst particles deactivated according to an industrially relevant protocol. New insights have been obtained by correlating Brønsted acidity changes, visualized using fluorescence microscopy, with structural transformations in the zeolite and matrix components, as observed with electron microscopy.
    PMID: 22213229 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575808</comments>
            <pubDate>Fri, 23 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5575808</guid>        </item>
        <item>
            <title>A Highly Diastereo- and Enantioselective Reaction for Constructing Functionalized Cyclohexanes: Six Contiguous Stereocenters in One Step.</title>
            <link>http://www.medworm.com/index.php?rid=5575807&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22213243%26dopt%3DAbstract</link>
            <description>Authors: Shi D, Xie Y, Zhou H, Xia C, Huang H
    Abstract
    Just mix to get six: Six contiguous stereocenters, including one quaternary stereocenter, and three CC bonds are created by a new copper-catalyzed tandem reaction. Rigid chiral diamine ligands enabled this asymmetric tandem reaction to proceed with excellent stereoselectivity (complete diastereoselectivity and high enantioselectivity) and high yield under mild reaction conditions.
    PMID: 22213243 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575807</comments>
            <pubDate>Fri, 23 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5575807</guid>        </item>
        <item>
            <title>Crystallographic Snapshots of the Bond-Breaking Isomerization Reactions Involving Nickel(II) Complexes with Hemilabile Ligands.</title>
            <link>http://www.medworm.com/index.php?rid=5575797&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22213388%26dopt%3DAbstract</link>
            <description>Authors: Machan CW, Lifschitz AM, Stern CL, Sarjeant AA, Mirkin CA
    Abstract
    Freeze-frame: Octahedral and square-planar structural isomers, representing the two &quot;end states&quot; in a hemilabile ligand bond-breaking isomerization reaction, have been characterized in solution by spectroscopic methods and in the solid state by X-ray crystallography (see picture: Ni green, C gray, P orange, N blue, S yellow).
    PMID: 22213388 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575797</comments>
            <pubDate>Fri, 23 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5575797</guid>        </item>
        <item>
            <title>Novel Strategies for Fluorine-18 Radiochemistry.</title>
            <link>http://www.medworm.com/index.php?rid=5575796&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22213395%26dopt%3DAbstract</link>
            <description>Authors: Littich R, Scott PJ
    Abstract
    Radiotracers: The growing demand for novel radiopharmaceuticals can only be met through the development of new approaches to isotopic labeling. Effective strategies and reagents for nucleophilic and electrophilic (18) F-radiolabeling are highlighted.
    PMID: 22213395 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575796</comments>
            <pubDate>Fri, 23 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5575796</guid>        </item>
        <item>
            <title>Aerobic Palladium(II)-Catalyzed 5-endo-trig Cyclization: An Entry into the Diastereoselective C-2 Alkenylation of Indoles with Tri- and Tetrasubstituted Double Bonds.</title>
            <link>http://www.medworm.com/index.php?rid=5575792&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22213474%26dopt%3DAbstract</link>
            <description>Authors: Kandukuri SR, Schiffner JA, Oestreich M
    Abstract
    The endo trick: An endo ring closure onto the trigonal β carbon atom of α,β-unsaturated acceptors that are tethered to the indole nitrogen atom followed by amide cleavage enables the diastereoselective C-2 alkenylation of indoles with fully substituted double bonds. The carboxy group functions as a synthetically useful temporary tether.
    PMID: 22213474 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575792</comments>
            <pubDate>Fri, 23 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5575792</guid>        </item>
        <item>
            <title>Triptycene Diols: A Strategy for Synthesizing Planar π Systems through Catalytic Conversion of a Poly(p-phenylene ethynylene) into a Poly(p-phenylene vinylene).</title>
            <link>http://www.medworm.com/index.php?rid=5575790&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22213522%26dopt%3DAbstract</link>
            <description>Authors: Vanveller B, Robinson D, Swager TM
    Abstract
    At level best: A strategic synthesis of a new class of poly(p-phenylene vinylene)-bearing annulated alkene units from a parent poly(p-phenylene ethynylene) is described. The gold-mediated cycloisomerization reaction of alkynes with appended hydroxy-group reacting partners delivers products having a stark increase in chain rigidity and planarity as evidenced by pronounced photophysical changes.
    PMID: 22213522 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575790</comments>
            <pubDate>Fri, 23 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5575790</guid>        </item>
        <item>
            <title>Deep-Tissue Photoacoustic Tomography of a Genetically Encoded Near-Infrared Fluorescent Probe.</title>
            <link>http://www.medworm.com/index.php?rid=5575788&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22213541%26dopt%3DAbstract</link>
            <description>Authors: Filonov GS, Krumholz A, Xia J, Yao J, Wang LV, Verkhusha VV
    Abstract
    Skin-deep: The combination of a near-infrared fluorescent protein (iRFP) and deep-tissue photoacoustic tomography clearly demonstrates the superiority of iRFP over other genetically encoded probes. Impressive resolution (280 μm lateral and 75 μm axial) was obtained at a depth of 4 mm in a live animal, and volumetric images of a tumor were produced, thus allowing the spatially resolved monitoring of its development.
    PMID: 22213541 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575788</comments>
            <pubDate>Fri, 23 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5575788</guid>        </item>
        <item>
            <title>Remarkable Adsorption Capacity of CuCl(2) -Loaded Porous Vanadium Benzenedicarboxylate for Benzothiophene.</title>
            <link>http://www.medworm.com/index.php?rid=5575786&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22213559%26dopt%3DAbstract</link>
            <description>Authors: Khan NA, Jhung SH
    Abstract
    Metal-organic frameworks loaded with cupric chloride are applied for adsorptive desulfurization. In their Communication (DOI: 10.1002/anie.201105113), N. A. Khan and S. H. Jhung report the remarkable adsorptive performance of CuCl(2) /V-benzenedicarboxylate (V-BDC) because of the facile reduction of Cu(II) to Cu(I) by V(III) of V-BDC. This approach provides new insights into redox reactions in metal-organic framework materials and can find application in the adsorptive desulfurization of liquid fuels.
    PMID: 22213559 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575786</comments>
            <pubDate>Fri, 23 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5575786</guid>        </item>
        <item>
            <title>A Synthetic Approach Toward a Self-Regulated Insulin Delivery System.</title>
            <link>http://www.medworm.com/index.php?rid=5575784&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22213580%26dopt%3DAbstract</link>
            <description>Authors: Matsumoto A, Ishii T, Nishida J, Matsumoto H, Kataoka K, Miyahara Y
    Abstract
    A totally synthetic artificial pancreas is described by Y. Miyahara et al. in their Communication (DOI: 10.1002/anie.201106252). A hydrogel bearing a phenylboronate derivative undergoes a glucose-dependent transition in its state of hydration under physiological conditions. The reversible surface-localized dehydration enables the provision of insulin to be controlled, thus offering a new basis for the treatment of diabetes with long-term stability and safety.
    PMID: 22213580 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575784</comments>
            <pubDate>Fri, 23 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5575784</guid>        </item>
        <item>
            <title>Competition and Cooperativity in Carbon Dioxide Sorption by Amine-Functionalized Metal-Organic Frameworks.</title>
            <link>http://www.medworm.com/index.php?rid=5575782&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22213592%26dopt%3DAbstract</link>
            <description>Authors: Vaidhyanathan R, Iremonger SS, Shimizu GK, Boyd PG, Alavi S, Woo TK
    Abstract
    Molecular insights into the roles of amine functionalization and cooperative CO(2) interactions into enhancing (and diminishing) CO(2) binding by metal-organic frameworks are shown both experimentally and computationally. Contrary to popular thinking, higher amination decreases CO(2) binding in this system. This loss is compensated by cooperativity between CO(2) triads that enhances binding by over 7 kJ mol(-1) .
    PMID: 22213592 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575782</comments>
            <pubDate>Fri, 23 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5575782</guid>        </item>
        <item>
            <title>Oligoprolines as Scaffolds for the Formation of Silver Nanoparticles in Defined Sizes-Correlating Molecular and Nanoscopic Dimensions.</title>
            <link>http://www.medworm.com/index.php?rid=5575780&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22213611%26dopt%3DAbstract</link>
            <description>Authors: Upert G, Bouillère F, Wennemers H
    Abstract
    Metallized scaffolds: Oligoproline scaffolds that are functionalized with aldehyde groups have been shown to control the size of silver nanoparticles that are formed in the Tollens reaction. The size of the nanoparticles correlates linearly with the length of the scaffold and the oxidation of the aldehyde moieties during the reaction helps to stabilize the nanoparticles through coordination to the newly formed carboxylic acid groups.
    PMID: 22213611 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575780</comments>
            <pubDate>Fri, 23 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5575780</guid>        </item>
        <item>
            <title>Controlled Doping of MS(2)  (M=W, Mo) Nanotubes and Fullerene-like Nanoparticles.</title>
            <link>http://www.medworm.com/index.php?rid=5575779&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22213621%26dopt%3DAbstract</link>
            <description>Controlled Doping of MS(2) (M=W, Mo) Nanotubes and Fullerene-like Nanoparticles.
    Angew Chem Int Ed Engl. 2011 Dec 23;
    Authors: Yadgarov L, Rosentsveig R, Leitus G, Albu-Yaron A, Moshkovich A, Perfilyev V, Vasic R, Frenkel AI, Enyashin AN, Seifert G, Rapoport L, Tenne R
    Abstract
    Lubricating nanoparticles: The effect of doping semiconductor hollow closed-fullerene-like nanoparticles of MoS(2) and WS(2) has been overlooked to date. Rhenium doping of these nanoparticles leads to a marked increase in the nanoparticle's conductivity, reduced agglomeration, and a great reduction in friction and wear that approaches superlubricity.
    PMID: 22213621 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575779</comments>
            <pubDate>Fri, 23 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5575779</guid>        </item>
        <item>
            <title>Fragment Deconstruction of Small, Potent Factor Xa Inhibitors: Exploring the Superadditivity Energetics of Fragment Linking in Protein-Ligand Complexes.</title>
            <link>http://www.medworm.com/index.php?rid=5575778&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22213624%26dopt%3DAbstract</link>
            <description>Authors: Nazaré M, Matter H, Will DW, Wagner M, Urmann M, Czech J, Schreuder H, Bauer A, Ritter K, Wehner V
    Abstract
    The superadditivity of fragment linking on affinities was quantified by systematic deconstruction of a fXa inhibitor. In their Communication (DOI: 10.1002/anie.201107091), M. Nazaré, H. Matter, and co-workers show that by connecting two fragments with a single bond, a linker contribution of -14.0 kJ mol(-1) results, which corresponds to an affinity improvement of about 2.5 orders of magnitude relative to the sum of fragment affinities.
    PMID: 22213624 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575778</comments>
            <pubDate>Fri, 23 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5575778</guid>        </item>
        <item>
            <title>The Triple Role of Fluoride Ions in Palladium-Catalyzed Suzuki-Miyaura Reactions: Unprecedented Transmetalation from [ArPdFL(2) ] Complexes.</title>
            <link>http://www.medworm.com/index.php?rid=5575777&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22213630%26dopt%3DAbstract</link>
            <description>Authors: Amatore C, Jutand A, Le Duc G
    Abstract
    Fluoride ions play three roles in the Suzuki-Miyaura reaction. They favor the reaction by formation of trans-[ArPdF(PPh(3) )(2) ], which reacts with Ar'B(OH)(2) in an unprecedented rate-determining transmetalation; and promoting the reductive elimination from the trans-[ArPdAr'(PPh(3) )(2) ] intermediate. Conversely, F(-) disfavors the reaction by formation of unreactive anionic Ar'B(OH)(n-3) F(n)       (-) (n=1-3), leading to two antagonistic effects of F(-) in the transmetalation.
    PMID: 22213630 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575777</comments>
            <pubDate>Fri, 23 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5575777</guid>        </item>
        <item>
            <title>Mesoporous Organosilica Hybrids Consisting of Silica-Wrapped π-π Stacking Columns.</title>
            <link>http://www.medworm.com/index.php?rid=5575776&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22213633%26dopt%3DAbstract</link>
            <description>Authors: Mizoshita N, Tani T, Shinokubo H, Inagaki S
    Abstract
    A new class of periodic mesoporous organosilica (PMO) materials with a columnar π-stacking arrangement of the framework organic groups have been prepared from disk-like precursors with hydrophobic perylene bisimide (PBI) cores. The PBI-bridged PMOs exhibit exciton coupling and efficient formation of mobile radical spins by electron doping within the pore walls.
    PMID: 22213633 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575776</comments>
            <pubDate>Fri, 23 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5575776</guid>        </item>
        <item>
            <title>Linking Ion and Neutral Chemistry in CH Bond Electrophilic Activation: Generation and Detection of HO(2)             (.)  Reactive Radicals in the Gas Phase.</title>
            <link>http://www.medworm.com/index.php?rid=5575774&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22213640%26dopt%3DAbstract</link>
            <description>Linking Ion and Neutral Chemistry in CH Bond Electrophilic Activation: Generation and Detection of HO(2)       (.) Reactive Radicals in the Gas Phase.
    Angew Chem Int Ed Engl. 2011 Dec 23;
    Authors: de Petris G, Angelini G, Ursini O, Rosi M, Troiani A
    Abstract
    The flip side: Both the charged and uncharged products formed by CH bond electrophilic activation have been experimentally detected in the gas phase. The HO(2)       (.) radical is formed by a process involving the prototypical oxygen-centered radical cation O(2)       (.)       (+) and the methane derivative CH(2) F(2) .
    PMID: 22213640 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575774</comments>
            <pubDate>Fri, 23 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5575774</guid>        </item>
        <item>
            <title>Formation of Enantiomeric Impeller-Like Helical Architectures by DNA Self-Assembly and Silica Mineralization.</title>
            <link>http://www.medworm.com/index.php?rid=5575773&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22213641%26dopt%3DAbstract</link>
            <description>Authors: Liu B, Han L, Che S
    Abstract
    Impeller-like helical DNA-silica complexes (see picture; green: silica) were synthesized in the presence of magnesium ions (a). DNA chiral packing and corresponding macroscopic helical morphologies are tuned by the change of reaction temperature, pH value, and molar ratio (b) of the quaternary ammonium (yellow)/phosphate group.
    PMID: 22213641 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575773</comments>
            <pubDate>Fri, 23 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5575773</guid>        </item>
        <item>
            <title>Strain-Induced Orientation-Selective Cutting of Graphene into Graphene Nanoribbons on Oxidation.</title>
            <link>http://www.medworm.com/index.php?rid=5575771&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22213650%26dopt%3DAbstract</link>
            <description>Authors: Ma L, Wang J, Ding F
    Abstract
    Cut to ribbons: Making atomically well controlled graphene nanoribbons (GNRs) is prerequisite for many graphene applications. Ab initio calculations reveal that, on applying a uniaxial external tensile strain, O atoms adsorbed on graphene form parallel epoxy chains, and subsequent cutting by oxygen attack gives GNRs instead of the quantum dots that are obtained from unstrained graphene.
    PMID: 22213650 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575771</comments>
            <pubDate>Fri, 23 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5575771</guid>        </item>
        <item>
            <title>Enhanced Binding Affinity, Remarkable Selectivity, and High Capacity of CO(2)  by Dual Functionalization of a rht-Type Metal-Organic Framework.</title>
            <link>http://www.medworm.com/index.php?rid=5575770&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22213672%26dopt%3DAbstract</link>
            <description>Enhanced Binding Affinity, Remarkable Selectivity, and High Capacity of CO(2) by Dual Functionalization of a rht-Type Metal-Organic Framework.
    Angew Chem Int Ed Engl. 2011 Dec 23;
    Authors: Li B, Zhang Z, Li Y, Yao K, Zhu Y, Deng Z, Yang F, Zhou X, Li G, Wu H, Nijem N, Chabal YJ, Lai Z, Han Y, Shi Z, Feng S, Li J
    Abstract
    Open and friendly: The smallest member of the rht-type metal-organic frameworks (MOFs, see picture) constructed by a hexacarboxylate ligand with a nitrogen-rich imino triazine backbone shows a significantly enhanced gas binding affinity relative to all other isoreticular rht-type MOFs. The high adsorption capacity and remarkable selectivity of CO(2) are attributed to the high density of open metal and Lewis basic sites in the framework.
    PMID: 22213672 [...</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575770</comments>
            <pubDate>Fri, 23 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5575770</guid>        </item>
        <item>
            <title>Enzymatic Total Synthesis of Defucogilvocarcin M and Its Implications for Gilvocarcin Biosynthesis.</title>
            <link>http://www.medworm.com/index.php?rid=5575769&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22223167%26dopt%3DAbstract</link>
            <description>Authors: Pahari P, Kharel MK, Shepherd MD, van Lanen SG, Rohr J
    Abstract
    Teamwork: Defucogilvocarcin M (1, see scheme) was synthesized in a one-pot, enzymatic reaction from acetyl-CoA and malonyl-CoA by a combination of 15 enzymes obtained from E. coli as well as the gilvocarcin, jadomycin, and ravidomycin biosynthetic pathways. The mixture of enzymes was systematically reduced and varied to further delineate the sequence of reactions in the complex, post-polyketide steps of gilvocarcin biosynthesis.
    PMID: 22223167 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575769</comments>
            <pubDate>Fri, 23 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5575769</guid>        </item>
        <item>
            <title>Palladium-Catalyzed Divergent Reactions of α-Diazocarbonyl Compounds with Allylic Esters: Construction of Quaternary Carbon Centers.</title>
            <link>http://www.medworm.com/index.php?rid=5575767&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22223221%26dopt%3DAbstract</link>
            <description>Authors: Chen ZS, Duan XH, Zhou PX, Ali S, Luo JY, Liang YM
    Abstract
    Take two: α-Diazocarbonyl compounds display a diverse pattern of reactivity upon palladium-catalyzed reaction with esters. Esters bearing an alkynyl group on the carbonyl carbon lead to two different CC bonds at the same carbon atom in a single operation through decarboxylation and migratory insertion, whereas aromatic and benzylic acid derivatives afford aromatic and benzylic esters bearing an O-substituted quaternary carbon center.
    PMID: 22223221 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575767</comments>
            <pubDate>Fri, 23 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5575767</guid>        </item>
        <item>
            <title>Ambident Reactivities of Methylhydrazines.</title>
            <link>http://www.medworm.com/index.php?rid=5575761&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22223457%26dopt%3DAbstract</link>
            <description>Authors: Nigst TA, Ammer J, Mayr H
    Abstract
    Kinetics versus thermodynamics: Methyl groups increase the nucleophilic reactivity of the substituted position of hydrazines and reduce the nucleophilicity of the adjacent nitrogen center. As a result, the tertiary nitrogen of 1,1-dimethylhydrazine is 3000 times more reactive than the NH(2) group, but under thermodynamic control substitution of an NH(2) proton occurs.
    PMID: 22223457 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575761</comments>
            <pubDate>Fri, 23 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5575761</guid>        </item>
        <item>
            <title>Monitoring of Liquid-Phase Organic Reactions by Photoelectron Spectroscopy.</title>
            <link>http://www.medworm.com/index.php?rid=5575760&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22223466%26dopt%3DAbstract</link>
            <description>Authors: Kolbeck C, Niedermaier I, Taccardi N, Schulz PS, Maier F, Wasserscheid P, Steinrück HP
    Abstract
    There are strings attached: After linking the reacting groups to head groups of ionic liquids to drastically lower the vapour pressures of the reactants, ordinary liquid-phase organic reactions can be monitored by in situ X-ray photoelectron spectroscopy. This approach is demonstrated for the nucleophilic substitution of an alkyl amine and an alkyl chloride moiety, which are attached to the cation and anion of ionic liquids, respectively.
    PMID: 22223466 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575760</comments>
            <pubDate>Fri, 23 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5575760</guid>        </item>
        <item>
            <title>Dynamically Tunable Protein Microlenses.</title>
            <link>http://www.medworm.com/index.php?rid=5575757&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22223512%26dopt%3DAbstract</link>
            <description>Authors: Sun YL, Dong WF, Yang RZ, Meng X, Zhang L, Chen QD, Sun HB
    Abstract
    Proteins have been used to construct biocompatible microdevices by using maskless femtosecond laser direct writing. In their Communication (DOI: 10.1002/anie.201105925), W. F. Dong, H. B. Sun, and co-workers report their strategy to produce microlenses from bovine serum albumin. The microlenses have controllable geometry as well as excellent imaging performance, and the focal length can be dynamically tuned by changing the pH of the surrounding solution.
    PMID: 22223512 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575757</comments>
            <pubDate>Fri, 23 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5575757</guid>        </item>
        <item>
            <title>Two Different Packing Arrangements of Antiparallel Polyalanine.</title>
            <link>http://www.medworm.com/index.php?rid=5575753&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22223629%26dopt%3DAbstract</link>
            <description>Authors: Asakura T, Okonogi M, Horiguchi K, Aoki A, Saitô H, Knight DP, Williamson MP
    Abstract
    Two β-sheet arrangements: Polyalanines have been shown to adopt two different antiparallel crystal packing arrangements, depending on the length of the polymers. Short polymers that contain six alanine residues or fewer adopt a rectangular packing arrangement, whereas longer polymers are packed in a staggered pattern. The elucidation of these structures may help to explain the physical and biological properties of polyalanines.
    PMID: 22223629 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5575753</comments>
            <pubDate>Fri, 23 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5575753</guid>        </item>
        <item>
            <title>Abstracts.</title>
            <link>http://www.medworm.com/index.php?rid=5544101&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22190541%26dopt%3DAbstract</link>
            <description>Authors: 
    PMID: 22190541 [PubMed - in process] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5544101</comments>
            <pubDate>Fri, 23 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5544101</guid>        </item>
        <item>
            <title>BaFeO(3) : A Ferromagnetic Iron Oxide.</title>
            <link>http://www.medworm.com/index.php?rid=5544100&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22190542%26dopt%3DAbstract</link>
            <description>Authors: Hayashi N, Yamamoto T, Kageyama H, Nishi M, Watanabe Y, Kawakami T, Matsushita Y, Fujimori A, Takano M
    Abstract
    Magnetic attraction: The cubic perovskite BaFeO(3) (see picture, Ba blue, Fe brown, O white), which is obtained by a low-temperature reaction using ozone as an oxidant, exhibits ferromagnetism with a fairly large moment of 3.5 μ(B) per Fe ion above a small critical field of approximately 0.3 T. This specific ferromagnetism is attributed to the enhancement of O→Fe charge transfer that arises from deepening of the Fe(4+) d levels.
    PMID: 22190542 [PubMed - in process] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5544100</comments>
            <pubDate>Fri, 23 Dec 2011 05:00:00 +0100</pubDate>
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        <item>
            <title>Preview: angew. Chem. Int. Ed. 1/2012.</title>
            <link>http://www.medworm.com/index.php?rid=5544099&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22190543%26dopt%3DAbstract</link>
            <description>Authors: 
    PMID: 22190543 [PubMed - in process] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5544099</comments>
            <pubDate>Fri, 23 Dec 2011 05:00:00 +0100</pubDate>
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            <title>&quot;Angew Chem Int Ed Engl&quot;[ta]; +208 new citations</title>
            <link>http://www.medworm.com/index.php?rid=5524653&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fsites%2Fentrez%3Fcmd%3DSearch%26db%3Dpubmed%26term%3D%28%2520%28%2522Angew%2520Chem%2520Int%2520Ed%2520Engl%2522%255Bta%255D%29%2520AND%2520%25222011%252F11%252F22%252021.36%2522%255BEDAT%255D%253A%25222011%252F12%252F22%252000.00%2522%255BEDAT%255D%29</link>
            <description>208 new pubmed citations were retrieved for your search.
Click on the search hyperlink below to display the complete search results:

&quot;Angew Chem Int Ed Engl&quot;[ta]
These pubmed results were generated on 2011/12/22PubMed, a service of the National Library of Medicine, includes over 15 million 
citations for biomedical articles back to the 1950's.
These citations are from MEDLINE and additional life science journals. 
PubMed includes links to many sites providing full text articles and other related resources. (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5524653</comments>
            <pubDate>Thu, 22 Dec 2011 05:00:00 +0100</pubDate>
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        <item>
            <title>Abstracts.</title>
            <link>http://www.medworm.com/index.php?rid=5436130&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22102335%26dopt%3DAbstract</link>
            <description>Authors: 
    PMID: 22102335 [PubMed - in process] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5436130</comments>
            <pubDate>Wed, 23 Nov 2011 02:36:22 +0100</pubDate>
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        <item>
            <title>Preview: angew. Chem. Int. Ed. 49/2011.</title>
            <link>http://www.medworm.com/index.php?rid=5436129&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22102336%26dopt%3DAbstract</link>
            <description>Authors: 
    PMID: 22102336 [PubMed - in process] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
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            <pubDate>Wed, 23 Nov 2011 02:36:12 +0100</pubDate>
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        <item>
            <title>Selective Host-Guest Binding of Anions without Auxiliary Hydrogen Bonds: Entropy as an Aid to Design.</title>
            <link>http://www.medworm.com/index.php?rid=5436134&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22095796%26dopt%3DAbstract</link>
            <description>Authors: Ursu A, Schmidtchen FP
    Abstract
    Entropy matters! In contrast to classic host-guest design, which employs dedicated enthalpic interactions of the binding partners, the novel electroneutral host 1 binds its anionic guests by virtue of an overwhelmingly positive entropy of association. The prime driving force is guest desolvation. Despite the total omission of hydrogen bonding, host 1 is one of the best electroneutral receptors known for binding anions in polar solution.
    PMID: 22095796 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
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            <pubDate>Fri, 18 Nov 2011 05:00:00 +0100</pubDate>
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        <item>
            <title>Scope and Mechanism of the (4+3) Cycloaddition Reaction of Furfuryl Cations.</title>
            <link>http://www.medworm.com/index.php?rid=5436133&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22095918%26dopt%3DAbstract</link>
            <description>Authors: Winne JM, Catak S, Waroquier M, Van Speybroeck V
    Abstract
    The method of choice for the preparation of six-membered rings is the (4+2) cycloaddition. The isoelectronic (4+3) cycloaddition between a diene and an allyl cation gives seven-membered rings, but the synthesis of suitable cationic reaction partners is challenging. In their Communication (DOI: 10.1002/anie.201104930) J. M. Winne et al. report a novel synthetic method that uses furfuryl alcohols as three-carbon dienophiles for the rapid assembly of cycloheptenes.
    PMID: 22095918 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5436133</comments>
            <pubDate>Fri, 18 Nov 2011 05:00:00 +0100</pubDate>
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        <item>
            <title>Convex Polyhedral Au@Pd Core-Shell Nanocrystals with High-Index Facets.</title>
            <link>http://www.medworm.com/index.php?rid=5436132&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22095936%26dopt%3DAbstract</link>
            <description>Authors: Kim D, Lee YW, Lee SB, Han SW
    Abstract
    The many faces of noble metals: Through the simultaneous reduction of Au and Pd ions in the presence of octahedral Au nanocrystal (NC) seeds, hexoctahedron-like convex Au@Pd core-shell NCs, enclosed predominantly by high-index {12 5 3} facets, were synthesized under aqueous room-temperature conditions. The convex Au@Pd NCs showed much higher electrocatalytic properties toward ethanol oxidation than other types of Au@Pd NCs.
    PMID: 22095936 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
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            <pubDate>Fri, 18 Nov 2011 05:00:00 +0100</pubDate>
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        <item>
            <title>Organic Mixed-Valence Compounds: A Playground for Electrons and Holes.</title>
            <link>http://www.medworm.com/index.php?rid=5436131&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22095940%26dopt%3DAbstract</link>
            <description>Authors: Heckmann A, Lambert C
    Abstract
    Mixed-valence (MV) compounds are excellent model systems for the investigation of basic electron-transfer (ET) or charge-transfer (CT) phenomena. These issues are important in complex biophysical processes such as photosynthesis as well as in artificial electronic devices that are based on organic conjugated materials. Organic MV compounds are effective hole-transporting materials in organic light emitting diodes (OLEDs), solar cells, and photochromic windows. However, the importance of organic mixed-valence chemistry should not be seen in terms of the direct applicability of these species but the wealth of knowledge about ET phenomena that has been gained through their study. The great variety of organic redox centers and spacer moieties tha...</description>
            <author>Angewandte Chemie</author>
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            <pubDate>Fri, 18 Nov 2011 05:00:00 +0100</pubDate>
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        <item>
            <title>Abstracts.</title>
            <link>http://www.medworm.com/index.php?rid=5410890&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22083853%26dopt%3DAbstract</link>
            <description>Authors: 
    PMID: 22083853 [PubMed - in process] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5410890</comments>
            <pubDate>Thu, 17 Nov 2011 05:43:49 +0100</pubDate>
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        <item>
            <title>Cobalt-catalyzed coupling of alkyl iodides with alkenes: deprotonation of hydridocobalt enables turnover.</title>
            <link>http://www.medworm.com/index.php?rid=5410889&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22083854%26dopt%3DAbstract</link>
            <description>Authors: Weiss ME, Kreis LM, Lauber A, Carreira EM
    PMID: 22083854 [PubMed - in process] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5410889</comments>
            <pubDate>Thu, 17 Nov 2011 05:43:38 +0100</pubDate>
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        <item>
            <title>Preview: angew. Chem. Int. Ed. 48/2011.</title>
            <link>http://www.medworm.com/index.php?rid=5410888&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22083855%26dopt%3DAbstract</link>
            <description>Authors: 
    PMID: 22083855 [PubMed - in process] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5410888</comments>
            <pubDate>Thu, 17 Nov 2011 05:43:28 +0100</pubDate>
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        <item>
            <title>Barcoded Nucleotides.</title>
            <link>http://www.medworm.com/index.php?rid=5410887&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22083884%26dopt%3DAbstract</link>
            <description>Authors: Baccaro A, Steck AL, Marx A
    PMID: 22083884 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5410887</comments>
            <pubDate>Mon, 14 Nov 2011 05:00:00 +0100</pubDate>
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        <item>
            <title>2,2'-Biphospholes: Building Blocks for Tuning the HOMO-LUMO Gap of π-Systems Using Covalent Bonding and Metal Coordination.</title>
            <link>http://www.medworm.com/index.php?rid=5410886&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22083902%26dopt%3DAbstract</link>
            <description>Authors: Chen H, Delaunay W, Yu L, Joly D, Wang Z, Li J, Wang Z, Lescop C, Tondelier D, Geffroy B, Duan Z, Hissler M, Mathey F, Réau R
    PMID: 22083902 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5410886</comments>
            <pubDate>Mon, 14 Nov 2011 05:00:00 +0100</pubDate>
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        <item>
            <title>Quinone-Based, Redox-Active Resorcin[4]arene Cavitands.</title>
            <link>http://www.medworm.com/index.php?rid=5410885&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22083938%26dopt%3DAbstract</link>
            <description>Authors: Pochorovski I, Boudon C, Gisselbrecht JP, Ebert MO, Schweizer WB, Diederich F
    PMID: 22083938 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5410885</comments>
            <pubDate>Mon, 14 Nov 2011 05:00:00 +0100</pubDate>
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        <item>
            <title>Cross-Coupling of Aryl Grignard Reagents with Aryl Iodides and Bromides through S(RN) 1 Pathway.</title>
            <link>http://www.medworm.com/index.php?rid=5410884&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22083948%26dopt%3DAbstract</link>
            <description>Authors: Shirakawa E, Hayashi Y, Itoh KI, Watabe R, Uchiyama N, Konagaya W, Masui S, Hayashi T
    PMID: 22083948 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5410884</comments>
            <pubDate>Mon, 14 Nov 2011 05:00:00 +0100</pubDate>
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        <item>
            <title>A General Strategy for the Perfluoroalkylation of Arenes and Arylbromides by Using Arylboronate Esters and [(phen)CuR(F) ].</title>
            <link>http://www.medworm.com/index.php?rid=5410883&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22083965%26dopt%3DAbstract</link>
            <description>Authors: Litvinas ND, Fier PS, Hartwig JF
    PMID: 22083965 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5410883</comments>
            <pubDate>Mon, 14 Nov 2011 05:00:00 +0100</pubDate>
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        <item>
            <title>Copper-Catalyzed Borylation Reactions of Alkynes and Arynes.</title>
            <link>http://www.medworm.com/index.php?rid=5410882&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22083973%26dopt%3DAbstract</link>
            <description>Authors: Yoshida H, Kawashima S, Takemoto Y, Okada K, Ohshita J, Takaki K
    PMID: 22083973 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
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            <pubDate>Mon, 14 Nov 2011 05:00:00 +0100</pubDate>
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        <item>
            <title>Guest-responsive Fluorescence of Inclusion Crystals with π-Stacked Supramolecular Beads.</title>
            <link>http://www.medworm.com/index.php?rid=5410881&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22083979%26dopt%3DAbstract</link>
            <description>Authors: Hinoue T, Miyata M, Hisaki I, Tohnai N
    PMID: 22083979 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
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            <pubDate>Mon, 14 Nov 2011 05:00:00 +0100</pubDate>
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        <item>
            <title>Abstracts.</title>
            <link>http://www.medworm.com/index.php?rid=5410934&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22069157%26dopt%3DAbstract</link>
            <description>Authors: 
    PMID: 22069157 [PubMed - in process] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
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        <comments>http://www.medworm.com/rss/comments.php?id=5410934</comments>
            <pubDate>Fri, 11 Nov 2011 05:00:00 +0100</pubDate>
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        <item>
            <title>Preview: angew. Chem. Int. Ed. 47/2011.</title>
            <link>http://www.medworm.com/index.php?rid=5410930&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22069158%26dopt%3DAbstract</link>
            <description>Authors: 
    PMID: 22069158 [PubMed - in process] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
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            <pubDate>Fri, 11 Nov 2011 05:00:00 +0100</pubDate>
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            <title>Palladium-Catalyzed Oxidative Arylalkylation of Activated Alkenes: Dual CH Bond Cleavage of an Arene and Acetonitrile.</title>
            <link>http://www.medworm.com/index.php?rid=5410903&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22076660%26dopt%3DAbstract</link>
            <description>Authors: Wu T, Mu X, Liu G
    PMID: 22076660 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
            <type>journals</type>
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            <pubDate>Fri, 11 Nov 2011 05:00:00 +0100</pubDate>
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            <title>Solution-Processed Reduced Graphene Oxide Films as Electronic Contacts for Molecular Monolayer Junctions.</title>
            <link>http://www.medworm.com/index.php?rid=5410902&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22076709%26dopt%3DAbstract</link>
            <description>Authors: Seo S, Min M, Lee J, Lee T, Choi SY, Lee H
    PMID: 22076709 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
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            <pubDate>Fri, 11 Nov 2011 05:00:00 +0100</pubDate>
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            <title>Gold-Catalyzed Intermolecular [4+2] and [2+2+2] Cycloadditions of Ynamides with Alkenes.</title>
            <link>http://www.medworm.com/index.php?rid=5410901&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22076738%26dopt%3DAbstract</link>
            <description>Authors: Dateer RB, Shaibu BS, Liu RS
    PMID: 22076738 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
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            <pubDate>Fri, 11 Nov 2011 05:00:00 +0100</pubDate>
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            <title>Stable Fluorophosphines: Predicted and Realized Ligands for Catalysis.</title>
            <link>http://www.medworm.com/index.php?rid=5410896&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22076744%26dopt%3DAbstract</link>
            <description>Authors: Fey N, Garland M, Hopewell JP, McMullin CL, Mastroianni S, Orpen AG, Pringle PG
    PMID: 22076744 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
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            <pubDate>Fri, 11 Nov 2011 05:00:00 +0100</pubDate>
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            <title>Synthesis of 5-Alkyl[3,4-c]thienopyrrole-4,6-dione-Based Polymers by Direct Heteroarylation.</title>
            <link>http://www.medworm.com/index.php?rid=5410893&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22076798%26dopt%3DAbstract</link>
            <description>Authors: Berrouard P, Najari A, Pron A, Gendron D, Morin PO, Pouliot JR, Veilleux J, Leclerc M
    PMID: 22076798 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
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            <pubDate>Fri, 11 Nov 2011 05:00:00 +0100</pubDate>
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            <title>Host-Guest Geometry in Pores of Zeolite ZSM-5 Spatially Resolved with Multiplex CARS Spectromicroscopy.</title>
            <link>http://www.medworm.com/index.php?rid=5410892&amp;cid=s_37501_59_f&amp;fid=37501&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22076803%26dopt%3DAbstract</link>
            <description>Authors: Domke KF, Day JP, Rago G, Riemer TA, Kox MH, Weckhuysen BM, Bonn M
    PMID: 22076803 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
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            <pubDate>Fri, 11 Nov 2011 05:00:00 +0100</pubDate>
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            <title>Characterization of the Reaction Path and Transition States for RNA Transphosphorylation Models from Theory and Experiment.</title>
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            <title>&quot;Angew Chem Int Ed Engl&quot;[ta]; +182 new citations</title>
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            <description>182 new pubmed citations were retrieved for your search.
Click on the search hyperlink below to display the complete search results:

&quot;Angew Chem Int Ed Engl&quot;[ta]
These pubmed results were generated on 2011/11/04PubMed, a service of the National Library of Medicine, includes over 15 million 
citations for biomedical articles back to the 1950's.
These citations are from MEDLINE and additional life science journals. 
PubMed includes links to many sites providing full text articles and other related resources. (Source: Angewandte Chemie)</description>
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            <description>Authors: Chen F, Qin C, Cui Y, Jiao N
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            <title>&quot;Angew Chem Int Ed Engl&quot;[ta]; +187 new citations</title>
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            <description>187 new pubmed citations were retrieved for your search.
Click on the search hyperlink below to display the complete search results:

&quot;Angew Chem Int Ed Engl&quot;[ta]
These pubmed results were generated on 2011/10/02PubMed, a service of the National Library of Medicine, includes over 15 million 
citations for biomedical articles back to the 1950's.
These citations are from MEDLINE and additional life science journals. 
PubMed includes links to many sites providing full text articles and other related resources. (Source: Angewandte Chemie)</description>
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            <pubDate>Sun, 02 Oct 2011 18:49:57 +0100</pubDate>
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            <title>Capture of Radioactive Cesium and Iodide Ions from Water by Using Titanate Nanofibers and Nanotubes.</title>
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            <description>Authors: Yang D, Sarina S, Zhu H, Liu H, Zheng Z, Xie M, Smith SV, Komarneni S
    PMID: 21932208 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
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            <pubDate>Tue, 20 Sep 2011 04:00:00 +0100</pubDate>
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            <title>Metal Nanoparticles Sensitize the Formation of Singlet Oxygen.</title>
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            <description>Authors: Vankayala R, Sagadevan A, Vijayaraghavan P, Kuo CL, Hwang KC
    PMID: 21932210 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
            <author>Angewandte Chemie</author>
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            <title>Scandium-Catalyzed Silylation of Aromatic CH Bonds.</title>
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            <description>Authors: Oyamada J, Nishiura M, Hou Z
    PMID: 21932221 [PubMed - as supplied by publisher] (Source: Angewandte Chemie)</description>
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