<?xml version="1.0" encoding="UTF-8"?>

<rdf:RDF
 xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#"
 xmlns="http://purl.org/rss/1.0/"
 xmlns:content="http://purl.org/rss/1.0/modules/content/"
 xmlns:taxo="http://purl.org/rss/1.0/modules/taxonomy/"
 xmlns:dc="http://purl.org/dc/elements/1.1/"
 xmlns:syn="http://purl.org/rss/1.0/modules/syndication/"
 xmlns:admin="http://webns.net/mvcb/"
>

<channel rdf:about="http://www.chempubsoc.eu/">
<title>Spotlights on Chemistry Journals by ChemPubSoc Europe / Wiley-VCH</title>
<link>http://www.chempubsoc.eu/</link>
<description>Selected content from chemistry journals published by Wiley-VCH with ChemPubSoc Europe</description>
<dc:language>en-us</dc:language>
<dc:rights>Copyright 2011, Wiley-VCH</dc:rights>
<dc:date>2012-02-08T04:19:18Z</dc:date>
<dc:publisher>Wiley-VCH</dc:publisher>
<dc:creator>mmueller@wiley-vch.de</dc:creator>
<dc:subject>Chemistry</dc:subject>
<syn:updateBase>2010-01-01T00:00+00:00</syn:updateBase>
<syn:updateFrequency>1</syn:updateFrequency>
<syn:updatePeriod>daily</syn:updatePeriod>
<items>
 <rdf:Seq>
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/anie.201103672" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/anie.201105719" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/anie.201106313" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/anie.201107900" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/asia.201100563" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/asia.201100632" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/asia.201100637" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/asia.201100681" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cbic.201100377" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cbic.201100578" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cbic.201100579" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cbic.201100603" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cctc.201100174" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cctc.201100221" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cctc.201100250" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cctc.201100281" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201102487" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201102494" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201102769" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/chem.201103090" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cmdc.201100317" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cmdc.201100338" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cmdc.201100358" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cmdc.201100372" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100446" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100454" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100504" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cphc.201100640" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cplu.201100007" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cplu.201100016" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cplu.201100026" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cssc.201100276" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cssc.201100281" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cssc.201100398" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/cssc.201100492" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201100700" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201100834" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201100890" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejic.201100894" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101057" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101215" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101249" />
  <rdf:li rdf:resource="http://dx.doi.org/10.1002/ejoc.201101284" />
 </rdf:Seq>
</items>
</channel>
<item rdf:about="http://dx.doi.org/10.1002/anie.201103672">
<title>Etiology of Potentially Primordial Biomolecular Structures: From Vitamin B&#x3C;sub&#x3E;12&#x3C;/sub&#x3E; to the Nucleic Acids and an Inquiry into the Chemistry of Life&#x2019;s Origin: A Retrospective</title>
<link>http://dx.doi.org/10.1002/anie.201103672</link>
<dc:creator>Albert Eschenmoser</dc:creator>
<dc:date>2011-12-07T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/anie.201103672.gif" alt="Etiology of Potentially Primordial Biomolecular Structures: From Vitamin B12 to the Nucleic Acids and an Inquiry into the Chemistry of Life&rsquo;s Origin: A Retrospective" style="float:left; padding-right: 10px" /></p><P><B>The quest for the etiology</B> of a biomolecular structure acquires special significance when the questions asked refer to molecules, the existence of which are fundamental to life, and in particular to the origin of life. In a search for the chemistry of the emergence of life, one needs to pay strict heed to molecular guides&mdash;nucleic acids, proteins, cofactors&mdash;that all carry a message, which is our job to decipher.</P><p>[Review]<br />Albert Eschenmoser<br /><i>Angew. Chem. Int. Ed.</i> <b>2011</b>, <i>50</i>, No. 52, 12412. <a href="http://dx.doi.org/10.1002/anie.201103672">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/anie.201105719">
<title>Molecular Details of the Recognition of Blood Group Antigens by a Human Norovirus as Determined by STD NMR Spectroscopy
</title>
<link>http://dx.doi.org/10.1002/anie.201105719</link>
<dc:creator>Brigitte Fiege, Christoph Rademacher, Jonathan Cartmell, Pavel I. Kitov, Francisco Parra, Thomas Peters</dc:creator>
<dc:date>2011-12-13T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/anie.201105719.gif" alt="Molecular Details of the Recognition of Blood Group Antigens by a Human Norovirus as Determined by STD NMR Spectroscopy
" style="float:left; padding-right: 10px" /></p><P><B>Tracing the infection</B>: The binding of human norovirus particles to blood group antigens was investigated using NMR spectroscopy. Binding epitopes were determined at atomic resolution, information on the binding specificity was obtained, and the bioactive conformation of various sugars was revealed. This provides valuable information for the design of entry inhibitors against this important class of human pathogenic viruses.</P><p>[Communication]<br />Brigitte Fiege, Christoph Rademacher, Jonathan Cartmell, Pavel I. Kitov, Francisco Parra, Thomas Peters<br /><i>Angew. Chem. Int. Ed.</i> <b>2012</b>, <i>51</i>, No. 4, 928. <a href="http://dx.doi.org/10.1002/anie.201105719">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/anie.201106313">
<title>ImmunoPods: Polymer Shells with Native Antibody Cross-Links
</title>
<link>http://dx.doi.org/10.1002/anie.201106313</link>
<dc:creator>Ke Zhang, Dan Zheng, Liangliang Hao, Joshua I. Cutler, Evelyn Auyeung, Chad A. Mirkin</dc:creator>
<dc:date>2011-12-15T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/anie.201106313.gif" alt="ImmunoPods: Polymer Shells with Native Antibody Cross-Links
" style="float:left; padding-right: 10px" /></p><P><B>Nanopods</B> functionalized with anti-HER2 antibodies (ImmunoPods, see scheme) have been synthesized by adsorbing the proteins onto gold nanoparticles and catalytically cross-linking them with a coadsorbed polymer through pendant propargyl ether groups. Upon dissolution of the gold template, the hollow polymer nanopod&ndash;protein conjugates remain. ImmunoPods are bioactive and can target cancer cells that express the HER2 antigen.</P><p>[Communication]<br />Ke Zhang, Dan Zheng, Liangliang Hao, Joshua I. Cutler, Evelyn Auyeung, Chad A. Mirkin<br /><i>Angew. Chem. Int. Ed.</i> <b>2012</b>, <i>51</i>, No. 5, 1169. <a href="http://dx.doi.org/10.1002/anie.201106313">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/anie.201107900">
<title>Fritz Haber: Flawed Greatness of Person and Country
</title>
<link>http://dx.doi.org/10.1002/anie.201107900</link>
<dc:creator>Fritz Stern</dc:creator>
<dc:date>2011-12-08T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/anie.201107900.gif" alt="Fritz Haber: Flawed Greatness of Person and Country
" style="float:left; padding-right: 10px" /></p><P><B>Onkel Fritz</B>: In his lecture at the Centennial Celebration of The Fritz Haber Institute, Fritz Stern reflects on the strengths and flaws of the Institute's founder. Can we judge a person without considering the historical and cultural context? In a sense, Haber's life encompassing triumph and tragedy is a reflection of his country at that time.</P><p>[Essay]<br />Fritz Stern<br /><i>Angew. Chem. Int. Ed.</i> <b>2012</b>, <i>51</i>, No. 1, 50. <a href="http://dx.doi.org/10.1002/anie.201107900">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/asia.201100563">
<title>Decoration of Diatom Biosilica with Noble Metal and Semiconductor Nanoparticles (&#x3C;10 nm): Assembly, Characterization, and Applications</title>
<link>http://dx.doi.org/10.1002/asia.201100563</link>
<dc:creator>Anne Jantschke, Anne-Kristin Herrmann, Vladimir Lesnyak, Alexander Eychm&#xFC;ller, Eike Brunner</dc:creator>
<dc:date>2011-11-18T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/asia.201100563.gif" alt="Decoration of Diatom Biosilica with Noble Metal and Semiconductor Nanoparticles (&lt;10 nm): Assembly, Characterization, and Applications" style="float:left; padding-right: 10px" /></p><P><B>Midas touch</B>: Diatom-templated noble metal (Ag, Pt, Au) and semiconductor (CdTe) nanoparticle arrays were synthesized by the attachment of prefabricated nanoparticles of defined size. The synthesized arrays were useful for surface-enhanced Raman spectroscopy (SERS) of components, for catalysis, and for the improvement of image quality in SEM.</P><p>[Full Paper]<br />Anne Jantschke, Anne-Kristin Herrmann, Vladimir Lesnyak, Alexander Eychm&uuml;ller, Eike Brunner<br /><i>Chem. Asian J.</i> <b>2012</b>, <i>7</i>, No. 1, 85. <a href="http://dx.doi.org/10.1002/asia.201100563">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/asia.201100632">
<title>New Azidotetrazoles: Structurally Interesting and Extremely Sensitive</title>
<link>http://dx.doi.org/10.1002/asia.201100632</link>
<dc:creator>Thomas M. Klap&#xF6;tke, Burkhard Krumm, Franz A. Martin, J&#xF6;rg Stierstorfer</dc:creator>
<dc:date>2011-11-09T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/asia.201100632.gif" alt="New Azidotetrazoles: Structurally Interesting and Extremely Sensitive" style="float:left; padding-right: 10px" /></p><P><B>Hypersensitivity</B>: 1-Amino-5-azidotetrazole (<B>1</B>), 5-azido-1-diazido-carbamoyltetrazole (<B>2</B>), and 1-(amino-azidocarbamoyl)-5-azidotetrazole (<B>3</B>) were formed by the diazotation of triaminoguanidinium chloride and separated by short-column chromatography. Their high nitrogen content results in extremely high sensitivity, therefore handling and characterization were very challenging.</P><p>[Full Paper]<br />Thomas M. Klap&ouml;tke, Burkhard Krumm, Franz A. Martin, J&ouml;rg Stierstorfer<br /><i>Chem. Asian J.</i> <b>2012</b>, <i>7</i>, No. 1, 214. <a href="http://dx.doi.org/10.1002/asia.201100632">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/asia.201100637">
<title>Selective, Cytotoxic Organoruthenium(II) Full-Sandwich Complexes: A Structural, Computational and In Vitro Biological Study</title>
<link>http://dx.doi.org/10.1002/asia.201100637</link>
<dc:creator>Bradley T. Loughrey, Benjamin V. Cunning, Peter C. Healy, Christopher L. Brown, Peter G. Parsons, Michael L. Williams</dc:creator>
<dc:date>2011-11-17T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/asia.201100637.gif" alt="Selective, Cytotoxic Organoruthenium(II) Full-Sandwich Complexes: A Structural, Computational and In Vitro Biological Study" style="float:left; padding-right: 10px" /></p><P><B>Ru positive?</B> A diverse range of lipophilic, cationic full-sandwich complexes of ruthenium(II) have been prepared and structurally characterized. Computational experiments predict each molecule to possess a delocalized &delta;+ electrostatic potential, and in vitro cytotoxicity studies demonstrate these lipophilic cations to be potent and selective growth inhibitors of tumorigenic cells lines.</P><p>[Full Paper]<br />Bradley T. Loughrey, Benjamin V. Cunning, Peter C. Healy, Christopher L. Brown, Peter G. Parsons, Michael L. Williams<br /><i>Chem. Asian J.</i> <b>2012</b>, <i>7</i>, No. 1, 112. <a href="http://dx.doi.org/10.1002/asia.201100637">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/asia.201100681">
<title>Nanoporous Carbon Materials for Electrochemical Sensing</title>
<link>http://dx.doi.org/10.1002/asia.201100681</link>
<dc:creator>Hwee Ling Poh, Martin Pumera</dc:creator>
<dc:date>2011-12-12T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/asia.201100681.gif" alt="Nanoporous Carbon Materials for Electrochemical Sensing" style="float:left; padding-right: 10px" /></p><P><B>A great sense of achievement!</B> The performance of nanoporous carbon as an electrode material was investigated and compared with that of bare glassy carbon, graphite microparticles, and carbon nanotubes. Nanoporous carbon was found to exhibit the highest heterogeneous electron transfer (HET) rate among these materials, thus sensing analytes such as NADH, DNA bases, and 2,4,6-trinitrotoluene (TNT) with an improved electrochemical response.</P><p>[Full Paper]<br />Hwee Ling Poh, Martin Pumera<br /><i>Chem. Asian J.</i> <b>2012</b>, <i>7</i>, No. 2, 412. <a href="http://dx.doi.org/10.1002/asia.201100681">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cbic.201100377">
<title>Intein-Mediated Construction of a Library of Fluorescent Rab GTPase Probes</title>
<link>http://dx.doi.org/10.1002/cbic.201100377</link>
<dc:creator>Yao-Wen Wu, Roger S. Goody, Kirill Alexandrov</dc:creator>
<dc:date>2011-11-15T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/cbic.201100377.gif" alt="Intein-Mediated Construction of a Library of Fluorescent Rab GTPase Probes" style="float:left; padding-right: 10px" /></p><P><B>Taking the Rab:</B> Expressed protein ligation allows site-specific incorporation of unnatural functionalities, such as fluorophores, into proteins. This requires synthesis of peptides with such functionalities and their subsequent ligation onto proteins. To construct a library of fluorescent RabGTPase sensors we developed an alternative approach in which proteins are labeled on a free cysteine and then ligated to an unlabeled peptide.</P><p>[Full Paper]<br />Yao-Wen Wu, Roger S. Goody, Kirill Alexandrov<br /><i>ChemBioChem</i> <b>2011</b>, <i>12</i>, No. 18, 2813. <a href="http://dx.doi.org/10.1002/cbic.201100377">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cbic.201100578">
<title>Photoswitchable Click Amino Acids: Light Control of Conformation and Bioactivity</title>
<link>http://dx.doi.org/10.1002/cbic.201100578</link>
<dc:creator>Christian Hoppmann, Peter Schmieder, Nadja Heinrich, Michael Beyermann</dc:creator>
<dc:date>2011-10-13T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/cbic.201100578.gif" alt="Photoswitchable Click Amino Acids: Light Control of Conformation and Bioactivity" style="float:left; padding-right: 10px" /></p><P><B>Click the switch:</B> By using a photoswitchable click amino acid (PSCaa) a light-induced intramolecular thiol-ene click reaction with a neighboring cysteine under very mild conditions results in an azobenzene bridge (see figure). By expanding the genetic code for PSCaa the specific incorporation of photoswitch units into proteins in living cells can result in an exciting approach for studying light-controllable activity, in vivo.</P><p>[Communication]<br />Christian Hoppmann, Peter Schmieder, Nadja Heinrich, Michael Beyermann<br /><i>ChemBioChem</i> <b>2011</b>, <i>12</i>, No. 17, 2555. <a href="http://dx.doi.org/10.1002/cbic.201100578">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cbic.201100579">
<title>Directed Evolution Strategies for Enantiocomplementary Haloalkane Dehalogenases: From Chemical Waste to Enantiopure Building Blocks</title>
<link>http://dx.doi.org/10.1002/cbic.201100579</link>
<dc:creator>Jan G. E. van Leeuwen, Hein J. Wijma, Robert J. Floor, Jan-Metske van der Laan, Dick B. Janssen</dc:creator>
<dc:date>2011-11-23T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/cbic.201100579.gif" alt="Directed Evolution Strategies for Enantiocomplementary Haloalkane Dehalogenases: From Chemical Waste to Enantiopure Building Blocks" style="float:left; padding-right: 10px" /></p><P><B>Waste not, want not:</B> A carefully optimized directed evolution strategy was used to obtain two enantiocomplementary haloalkane dehalogenase variants that convert the toxic waste compound 1,2,3-trichloropropane into either (<I>R</I>)- or (<I>S</I>)-2,3-dichloropropan-1-ol. The products can be converted into optically active epichlorohydrins that could be used for the preparation of various chiral pharmaceuticals.</P><p>[Full Paper]<br />Jan G. E. van Leeuwen, Hein J. Wijma, Robert J. Floor, Jan-Metske van der Laan, Dick B. Janssen<br /><i>ChemBioChem</i> <b>2012</b>, <i>13</i>, No. 1, 137. <a href="http://dx.doi.org/10.1002/cbic.201100579">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cbic.201100603">
<title>Bromomaleimide-Linked Bioconjugates Are Cleavable in Mammalian Cells</title>
<link>http://dx.doi.org/10.1002/cbic.201100603</link>
<dc:creator>Paul Moody, Mark. E. B. Smith, Chris P. Ryan, Vijay Chudasama, James R. Baker, Justin Molloy, Stephen Caddick</dc:creator>
<dc:date>2011-11-18T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/cbic.201100603.gif" alt="Bromomaleimide-Linked Bioconjugates Are Cleavable in Mammalian Cells" style="float:left; padding-right: 10px" /></p><P><B>Bromomaleimides are versatile scaffolds</B> that allow facile conjugation of thiolated biomolecules. Here we demonstrate that bromomaleimide-linked GFP&ndash;rhodamine FRET pairs cleave in the cytoplasm of mammalian cells. We believe that bromomaleimide scaffolds provide a potential core structure for prodrugs designed to release bioactive cargo following cell internalisation.</P><p>[Communication]<br />Paul Moody, Mark. E. B. Smith, Chris P. Ryan, Vijay Chudasama, James R. Baker, Justin Molloy, Stephen Caddick<br /><i>ChemBioChem</i> <b>2012</b>, <i>13</i>, No. 1, 39. <a href="http://dx.doi.org/10.1002/cbic.201100603">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cctc.201100174">
<title>Application of Hierarchical Porous Silica with a Stable Large Porosity for &#x3B2;-Galactosidase Immobilization</title>
<link>http://dx.doi.org/10.1002/cctc.201100174</link>
<dc:creator>Claudia Bernal, Ligia Sierra, Monica Mesa</dc:creator>
<dc:date>2011-09-23T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/cctc.201100174.gif" alt="Application of Hierarchical Porous Silica with a Stable Large Porosity for &beta;-Galactosidase Immobilization" style="float:left; padding-right: 10px" /></p><P><B>Pin that enzyme down:</B> Hierarchical porous silica, synthesized by using sodium silicate, is used as support for immobilization of &beta;-galactosidase by the adsorption pathway. Their loading capacity and enzyme retention are explained in terms of their large mesopores and macropores and the surface silanol groups. Under extreme conditions, the hybrid biocatalyst is more stable than the soluble &beta;-galactosidase.</P><p>[Full Paper]<br />Claudia Bernal, Ligia Sierra, Monica Mesa<br /><i>ChemCatChem</i> <b>2011</b>, <i>3</i>, No. 12, 1948. <a href="http://dx.doi.org/10.1002/cctc.201100174">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cctc.201100221">
<title>Catalytic Aminolysis (Amide Formation) from Esters and Carboxylic Acids: Mechanism, Enhanced Ionic Liquid Effect, and its Origin</title>
<link>http://dx.doi.org/10.1002/cctc.201100221</link>
<dc:creator>Vanda Maria de Oliveira, Richard Silva de Jesus, Alexandre F. Gomes, F&#xE1;bio C. Gozzo, Alexandre P. Umpierre, Paulo A. Z. Suarez, Joel C. Rubim, Brenno A. D. Neto</dc:creator>
<dc:date>2011-10-26T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/cctc.201100221.gif" alt="Catalytic Aminolysis (Amide Formation) from Esters and Carboxylic Acids: Mechanism, Enhanced Ionic Liquid Effect, and its Origin" style="float:left; padding-right: 10px" /></p><P><B>Amides ride the ionic liquid cycles:</B> A novel catalytic method to perform amide bond formation from esters and carboxylic acids in ionic liquids is described. Mechanistic studies and the ionic liquid effect are also investigated. Recycling reactions are performed successfully. NMR and electrospray ionization&ndash;quadrupole time-of-flight experiments allowed for the proposition of a catalytic cycle to explain the reaction with Br&oslash;nsted acids, such as SnCl<sub>2</sub> and CdO.</P><p>[Full Paper]<br />Vanda Maria de Oliveira, Richard Silva de Jesus, Alexandre F. Gomes, F&aacute;bio C. Gozzo, Alexandre P. Umpierre, Paulo A. Z. Suarez, Joel C. Rubim, Brenno A. D. Neto<br /><i>ChemCatChem</i> <b>2011</b>, <i>3</i>, No. 12, 1911. <a href="http://dx.doi.org/10.1002/cctc.201100221">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cctc.201100250">
<title>Recycling Chiral Copper Bis(oxazoline) Complexes in an Original Multireaction Procedure</title>
<link>http://dx.doi.org/10.1002/cctc.201100250</link>
<dc:creator>Dorian Didier, Emmanuelle Schulz</dc:creator>
<dc:date>2011-10-12T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/cctc.201100250.gif" alt="Recycling Chiral Copper Bis(oxazoline) Complexes in an Original Multireaction Procedure" style="float:left; padding-right: 10px" /></p><P><B>Precipitation&ndash;the solution?</B> The recovery of a chiral copper(II) bis(oxazoline) catalyst by charge-transfer complexation and subsequent precipitation allows its efficient reuse in ene and cyclopropanation reactions for up to ten successive catalytic cycles and affords the desired products in high yields and enantioselectivities. The same catalyst batch is also successfully reused in three different asymmetric transformations in an original multireaction procedure.</P><p>[Communication]<br />Dorian Didier, Emmanuelle Schulz<br /><i>ChemCatChem</i> <b>2011</b>, <i>3</i>, No. 12, 1880. <a href="http://dx.doi.org/10.1002/cctc.201100250">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cctc.201100281">
<title>Synthesis of Titanium Chabazite: A New Shape Selective Oxidation Catalyst with Small Pore Openings and Application in the Production of Methyl Formate from Methanol</title>
<link>http://dx.doi.org/10.1002/cctc.201100281</link>
<dc:creator>Einar Andr&#xE9; Eilertsen, Silvia Bordiga, Carlo Lamberti, Alessandro Damin, Francesca Bonino, Bj&#xF8;rnar Arstad, Stian Svelle, Unni Olsbye, Karl Petter Lillerud</dc:creator>
<dc:date>2011-09-28T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/cctc.201100281.gif" alt="Synthesis of Titanium Chabazite: A New Shape Selective Oxidation Catalyst with Small Pore Openings and Application in the Production of Methyl Formate from Methanol" style="float:left; padding-right: 10px" /></p><P><B>Take CHAnce on zeolites:</B> A new titanium silicate oxidation catalyst (Ti-CHA) and a bifunctional titanium aluminum silicate catalyst (Ti-Al-CHA) with the chabazite (CHA) topology have been synthesized. The materials have a 3-dimensional channel system with small pore openings that enable shape selective oxidation catalysis. The new Ti-Al-CHA material facilitates a high conversion of methanol to methyl formate with a selectivity of 85 % at 60 &deg;C, using H<sub>2</sub>O<sub>2</sub> as the oxidation agent.</P><p>[Communication]<br />Einar Andr&eacute; Eilertsen, Silvia Bordiga, Carlo Lamberti, Alessandro Damin, Francesca Bonino, Bj&oslash;rnar Arstad, Stian Svelle, Unni Olsbye, Karl Petter Lillerud<br /><i>ChemCatChem</i> <b>2011</b>, <i>3</i>, No. 12, 1869. <a href="http://dx.doi.org/10.1002/cctc.201100281">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/chem.201102487">
<title>From Molecule to Materials: Crystalline Superlattices of Nanoscopic CdS Clusters</title>
<link>http://dx.doi.org/10.1002/chem.201102487</link>
<dc:creator>Tetyana I. Levchenko, Christian K&#xFC;bel, Yining Huang, John F. Corrigan</dc:creator>
<dc:date>2011-11-18T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/chem.201102487.gif" alt="From Molecule to Materials: Crystalline Superlattices of Nanoscopic CdS Clusters" style="float:left; padding-right: 10px" /></p><P><B>Make way for a superlattice!</B> A crystalline 3D superlattice of 2.3 nm molecular CdS nanoclusters was prepared from a convenient mononuclear cadmium thiophenolate precursor. HRTEM and STEM tomography show highly crystalline repetition of monodisperse frameworks (see figure). This combined with elemental and thermogravimetric analyses suggests an approximate formula [Cd<sub>130</sub>S<sub>103</sub>(SPh)<sub>54</sub>].</P><p>[Communication]<br />Tetyana I. Levchenko, Christian K&uuml;bel, Yining Huang, John F. Corrigan<br /><i>Chem. Eur. J.</i> <b>2011</b>, <i>17</i>, No. 51, 14394. <a href="http://dx.doi.org/10.1002/chem.201102487">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/chem.201102494">
<title>Mechanistic Aspects and Elementary Steps of N-H Bond Activation of Ammonia and C-N Coupling Induced by Gas-Phase Ions: A Combined Experimental/Computational Exercise</title>
<link>http://dx.doi.org/10.1002/chem.201102494</link>
<dc:creator>Robert Kretschmer, Maria Schlangen, Helmut Schwarz</dc:creator>
<dc:date>2011-12-05T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/chem.201102494.gif" alt="Mechanistic Aspects and Elementary Steps of N-H Bond Activation of Ammonia and C-N Coupling Induced by Gas-Phase Ions: A Combined Experimental/Computational Exercise" style="float:left; padding-right: 10px" /></p><P><B>Step by step</B>: Due to its extraordinary potential, N-H bond activation and C-N coupling processes have formed the focus of broad research activities. This Minireview will describe examples of these processes mediated by gaseous &ldquo;bare&rdquo; or ligated ions and provide detailed insights into the underlying mechanisms and elementary steps.</P><p>[Minireview]<br />Robert Kretschmer, Maria Schlangen, Helmut Schwarz<br /><i>Chem. Eur. J.</i> <b>2012</b>, <i>18</i>, No. 1, 40. <a href="http://dx.doi.org/10.1002/chem.201102494">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/chem.201102769">
<title>Drug Delivery and Imaging with Polydiacetylene Micelles
</title>
<link>http://dx.doi.org/10.1002/chem.201102769</link>
<dc:creator>Edmond Gravel, Julien Ogier, Thomas Arnauld, Nicolas Mackiewicz, Fr&#xE9;d&#xE9;ric Ducong&#xE9;, Eric Doris</dc:creator>
<dc:date>2011-12-02T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/chem.201102769.gif" alt="Drug Delivery and Imaging with Polydiacetylene Micelles
" style="float:left; padding-right: 10px" /></p><P><B>Photopolymerized micelles</B> obtained from the self-assembly of diacetylene-containing amphiphiles have been developed for biomedical applications in the fields of imaging and drug delivery (see figure).</P><p>[Concept]<br />Edmond Gravel, Julien Ogier, Thomas Arnauld, Nicolas Mackiewicz, Fr&eacute;d&eacute;ric Ducong&eacute;, Eric Doris<br /><i>Chem. Eur. J.</i> <b>2012</b>, <i>18</i>, No. 2, 400. <a href="http://dx.doi.org/10.1002/chem.201102769">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/chem.201103090">
<title>A Perylene Diimide Rotaxane: Synthesis, Structure and Electrochemically Driven De-Threading</title>
<link>http://dx.doi.org/10.1002/chem.201103090</link>
<dc:creator>Benjamin J. Slater, E. Stephen Davies, Stephen P. Argent, Harriott Nowell, William Lewis, Alexander J. Blake, Neil R. Champness</dc:creator>
<dc:date>2011-12-01T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/chem.201103090.gif" alt="A Perylene Diimide Rotaxane: Synthesis, Structure and Electrochemically Driven De-Threading" style="float:left; padding-right: 10px" /></p><P><B>Perylene diimides</B> make excellent building blocks for the formation of [2]-rotaxanes. The rich electrochemistry of the perylene-based recognition site facilitates a pathway to different oxidation states and properties and allows a mechanism for electrochemically driven de-treading of the interlocked species (see figure).</P><p>[Full Paper]<br />Benjamin J. Slater, E. Stephen Davies, Stephen P. Argent, Harriott Nowell, William Lewis, Alexander J. Blake, Neil R. Champness<br /><i>Chem. Eur. J.</i> <b>2011</b>, <i>17</i>, No. 52, 14746. <a href="http://dx.doi.org/10.1002/chem.201103090">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cmdc.201100317">
<title>Structure-Based Discovery of Allosteric Modulators of Two Related Class B G-Protein-Coupled Receptors</title>
<link>http://dx.doi.org/10.1002/cmdc.201100317</link>
<dc:creator>Chris de Graaf, Chantal Rein, David Piwnica, Fabrizio Giordanetto, Didier Rognan</dc:creator>
<dc:date>2011-10-12T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/cmdc.201100317.gif" alt="Structure-Based Discovery of Allosteric Modulators of Two Related Class B G-Protein-Coupled Receptors" style="float:left; padding-right: 10px" /></p><P><B>Virtual reality:</B> Although crystallographic structure data and related information have been reported for class A GPCRs, herein we report the first use of structure-based virtual screening to identify new allosteric modulators of class B GPCRs. Despite the modest activities of the identified compounds, this study provides a novel in silico approach for the discovery of future class B GPCR modulators.</P><p>[Full Paper]<br />Chris de Graaf, Chantal Rein, David Piwnica, Fabrizio Giordanetto, Didier Rognan<br /><i>ChemMedChem</i> <b>2011</b>, <i>6</i>, No. 12, 2159. <a href="http://dx.doi.org/10.1002/cmdc.201100317">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cmdc.201100338">
<title>Urolithin as a Converging Scaffold Linking Ellagic acid and Coumarin Analogues: Design of Potent Protein Kinase CK2 Inhibitors</title>
<link>http://dx.doi.org/10.1002/cmdc.201100338</link>
<dc:creator>Giorgio Cozza, Alessandra Gianoncelli, Paolo Bonvini, Elisa Zorzi, Riccardo Pasquale, Angelo Rosolen, Lorenzo A. Pinna, Flavio Meggio, Giuseppe Zagotto, Stefano Moro</dc:creator>
<dc:date>2011-10-04T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/cmdc.201100338.gif" alt="Urolithin as a Converging Scaffold Linking Ellagic acid and Coumarin Analogues: Design of Potent Protein Kinase CK2 Inhibitors" style="float:left; padding-right: 10px" /></p><P><B>Two become one:</B> Comparing the crystallographic binding modes of ellagic acid (red) and 3,8-dibromo-7-hydroxy-4-methylchromen-2-one (DBC; blue), an X-ray structure-driven merging approach to the design of novel casein kinase 2 (CK2) inhibitors was taken. Using this strategy, a potent and selective urolithin derivative, 4-bromo-3,8-dihydroxy-benzo[<I>c</I>]chromen-6-one was identified, which exhibits a <I>K</I><sub>i</sub> value of 7 n<span style="font-variant:small-caps">M</span> against CK2.</P><p>[Full Paper]<br />Giorgio Cozza, Alessandra Gianoncelli, Paolo Bonvini, Elisa Zorzi, Riccardo Pasquale, Angelo Rosolen, Lorenzo A. Pinna, Flavio Meggio, Giuseppe Zagotto, Stefano Moro<br /><i>ChemMedChem</i> <b>2011</b>, <i>6</i>, No. 12, 2273. <a href="http://dx.doi.org/10.1002/cmdc.201100338">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cmdc.201100358">
<title>A Comparison of Linear and Cyclic Peptoid Oligomers as Potent Antimicrobial Agents</title>
<link>http://dx.doi.org/10.1002/cmdc.201100358</link>
<dc:creator>Mia Lace Huang, Sung Bin Y. Shin, Meredith A. Benson, Victor J. Torres, Kent Kirshenbaum</dc:creator>
<dc:date>2011-09-23T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/cmdc.201100358.gif" alt="A Comparison of Linear and Cyclic Peptoid Oligomers as Potent Antimicrobial Agents" style="float:left; padding-right: 10px" /></p><P><B>Cycling builds endurance!</B> A family of linear N-substituted glycine &ldquo;peptoid&rdquo; oligomers bearing cationic and hydrophobic side chains were subjected to macrocyclization, thereby enhancing antimicrobial potency. These compounds are active against Gram-negative and Gram-positive bacteria and are non- hemolytic toward human erythrocytes.</P><p>[Full Paper]<br />Mia Lace Huang, Sung Bin Y. Shin, Meredith A. Benson, Victor J. Torres, Kent Kirshenbaum<br /><i>ChemMedChem</i> <b>2012</b>, <i>7</i>, No. 1, 114. <a href="http://dx.doi.org/10.1002/cmdc.201100358">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cmdc.201100372">
<title>Development of Isoxazoline-Containing Peptidomimetics as Dual &#x3B1;&#x3C;sub&#x3E;v&#x3C;/sub&#x3E;&#x3B2;&#x3C;sub&#x3E;3&#x3C;/sub&#x3E; and &#x3B1;&#x3C;sub&#x3E;5&#x3C;/sub&#x3E;&#x3B2;&#x3C;sub&#x3E;1&#x3C;/sub&#x3E; Integrin Ligands</title>
<link>http://dx.doi.org/10.1002/cmdc.201100372</link>
<dc:creator>Alessandra Tolomelli, Luca Gentilucci, Elisa Mosconi, Angelo Viola, Samantha Deianira Dattoli, Monica Baiula, Santi Spampinato, Laura Belvisi, Monica Civera</dc:creator>
<dc:date>2011-09-26T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/cmdc.201100372.gif" alt="Development of Isoxazoline-Containing Peptidomimetics as Dual &alpha;v&beta;3 and &alpha;5&beta;1 Integrin Ligands" style="float:left; padding-right: 10px" /></p><P><B>Molecular copycats!</B> Isoxazoline-containing peptidomimetics, designed to be effective &alpha;<sub>v</sub>&beta;<sub>3</sub> and &alpha;<sub>5</sub>&beta;<sub>1</sub> integrin ligands, were synthesized by hydroxyamine conjugate addition to alkylidene acetoacetates followed by intramolecular hemiketalization. Cell adhesion assay results suggest a very effective ligand&ndash;receptor interaction, as confirmed by docking studies.</P><p>[Full Paper]<br />Alessandra Tolomelli, Luca Gentilucci, Elisa Mosconi, Angelo Viola, Samantha Deianira Dattoli, Monica Baiula, Santi Spampinato, Laura Belvisi, Monica Civera<br /><i>ChemMedChem</i> <b>2011</b>, <i>6</i>, No. 12, 2264. <a href="http://dx.doi.org/10.1002/cmdc.201100372">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100446">
<title>NMR and MRI of Blood-Dissolved Hyperpolarized Xe-129 in Different Hollow-Fiber Membranes</title>
<link>http://dx.doi.org/10.1002/cphc.201100446</link>
<dc:creator>Nadia Amor, Kathrin Hamilton, Markus K&#xFC;ppers, Ulrich Steinseifer, Stephan Appelt, Bernhard Bl&#xFC;mich, Thomas Schmitz-Rode</dc:creator>
<dc:date>2011-10-12T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/cphc.201100446.gif" alt="NMR and MRI of Blood-Dissolved Hyperpolarized Xe-129 in Different Hollow-Fiber Membranes" style="float:left; padding-right: 10px" /></p><P><B>In the blood:</B> Hollow-fiber membranes for continuous dissolution of hyperpolarized xenon gas into blood are investigated via NMR spectroscopy and imaging with a xenonizer setup (see picture). Spatially resolved functionality is analyzed and a comparison of different fiber materials is presented.</P><p>[Article]<br />Nadia Amor, Kathrin Hamilton, Markus K&uuml;ppers, Ulrich Steinseifer, Stephan Appelt, Bernhard Bl&uuml;mich, Thomas Schmitz-Rode<br /><i>ChemPhysChem</i> <b>2011</b>, <i>12</i>, No. 16, 2941. <a href="http://dx.doi.org/10.1002/cphc.201100446">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100454">
<title>Nitrogen-Doped Carbon Nanotubes: Growth, Mechanism and Structure</title>
<link>http://dx.doi.org/10.1002/cphc.201100454</link>
<dc:creator>Justin P. O&#x27;Byrne, Zhonglai Li, Sarah L. T. Jones, Peter G. Fleming, J. Andreas Larsson, Michael A. Morris, Justin D. Holmes</dc:creator>
<dc:date>2011-10-14T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/cphc.201100454.gif" alt="Nitrogen-Doped Carbon Nanotubes: Growth, Mechanism and Structure" style="float:left; padding-right: 10px" /></p><P><B>Bamboo nanostructures:</B> Nitrogen-doped bamboo-structured carbon nanotubes are successfully grown using a series of cobalt/molybdenum catalysts (see picture). The growth of bamboo-structured nanotubes in the presence of nitrogen, in preference to single-walled and multi-walled nanotubes, is due to the greater binding energy of nitrogen for cobalt in the catalyst compared to the binding strength of carbon to cobalt, as determined by density functional theory.</P><p>[Article]<br />Justin P. O'Byrne, Zhonglai Li, Sarah L. T. Jones, Peter G. Fleming, J. Andreas Larsson, Michael A. Morris, Justin D. Holmes<br /><i>ChemPhysChem</i> <b>2011</b>, <i>12</i>, No. 16, 2995. <a href="http://dx.doi.org/10.1002/cphc.201100454">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100504">
<title>The Chemistry of Bioluminescence: An Analysis of Chemical Functionalities</title>
<link>http://dx.doi.org/10.1002/cphc.201100504</link>
<dc:creator>Isabelle Navizet, Ya-Jun Liu, Nicolas Ferr&#xE9;, Daniel Roca-Sanju&#xE1;n, Roland Lindh</dc:creator>
<dc:date>2011-10-13T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/cphc.201100504.gif" alt="The Chemistry of Bioluminescence: An Analysis of Chemical Functionalities" style="float:left; padding-right: 10px" /></p><P><B>Evolution of oxyluciferin:</B> Starting from simple models expanding to more complex ones (see picture) this review shows how theoretical calculations give insights for the color modulation of firefly luciferin.</P><p>[Review]<br />Isabelle Navizet, Ya-Jun Liu, Nicolas Ferr&eacute;, Daniel Roca-Sanju&aacute;n, Roland Lindh<br /><i>ChemPhysChem</i> <b>2011</b>, <i>12</i>, No. 17, 3064. <a href="http://dx.doi.org/10.1002/cphc.201100504">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201100640">
<title>Carbon Nanoparticles as Chromophores for Photon Harvesting and Photoconversion</title>
<link>http://dx.doi.org/10.1002/cphc.201100640</link>
<dc:creator>Juan Xu, Sushant Sahu, Li Cao, Parambath Anilkumar, Kenneth N. Tackett, IIHaijun Qian, Christopher E. Bunker, Elena A. Guliants, Alexander Parenzan, Ya-Ping Sun</dc:creator>
<dc:date>2011-10-13T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/cphc.201100640.gif" alt="Carbon Nanoparticles as Chromophores for Photon Harvesting and Photoconversion" style="float:left; padding-right: 10px" /></p><P><B>Undercover:</B> Carbon nanoparticles have recently emerged as a unique class of optical nanomaterials. This study demonstrates the chromophoric functions of suspended small carbon nanoparticles in harvesting visible photons for the reductive coating of the nanoparticles with silver and gold (see picture) and, as a result, the preparation of unique carbon-metal core&ndash;shell nanostructures.</P><p>[Article]<br />Juan Xu, Sushant Sahu, Li Cao, Parambath Anilkumar, Kenneth N. Tackett, IIHaijun Qian, Christopher E. Bunker, Elena A. Guliants, Alexander Parenzan, Ya-Ping Sun<br /><i>ChemPhysChem</i> <b>2011</b>, <i>12</i>, No. 18, 3604. <a href="http://dx.doi.org/10.1002/cphc.201100640">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cplu.201100007">
<title>Electrical Bistability and WORM Memory Effects in Donor&#x2013;Acceptor Polymers Based on Poly(&#x3C;I&#x3E;N&#x3C;/I&#x3E;-vinylcarbazole)
</title>
<link>http://dx.doi.org/10.1002/cplu.201100007</link>
<dc:creator>Bin Zhang, Gang Liu, Yu Chen, Cheng Wang, Koon-Gee Neoh, Ting Bai, En-Tang Kang</dc:creator>
<dc:date>2011-12-16T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/cplu.201100007.gif" alt="Electrical Bistability and WORM Memory Effects in Donor&ndash;Acceptor Polymers Based on Poly(N-vinylcarbazole)
" style="float:left; padding-right: 10px" /></p><P><B>Make the switch</B>: Poly(<I>N</I>-vinylcarbazole) derivatives with pendant donor&ndash;trap&ndash;acceptor structures exhibit electrical effects. The origin of the electrical bistability, which arises from the intramolecular charge transfer, trapping, and conformational relaxation of the electrostatic energy of the Al/polymer/indium tin oxide sandwich structure (see figure), was established by spectroscopic, microscopic, and molecular computational techniques.</P><p>[Full Paper]<br />Bin Zhang, Gang Liu, Yu Chen, Cheng Wang, Koon-Gee Neoh, Ting Bai, En-Tang Kang<br /><i>ChemPlusChem</i> <b>2012</b>, <i>77</i>, No. 1, 74. <a href="http://dx.doi.org/10.1002/cplu.201100007">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cplu.201100016">
<title>Gold Nanospacers Greatly Enhance the Capacitance of Electrochemically Reduced Graphene</title>
<link>http://dx.doi.org/10.1002/cplu.201100016</link>
<dc:creator>Lucia Buglione, Alessandra Bonanni, Adriano Ambrosi, Martin Pumera</dc:creator>
<dc:date>2011-12-16T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/cplu.201100016.gif" alt="Gold Nanospacers Greatly Enhance the Capacitance of Electrochemically Reduced Graphene" style="float:left; padding-right: 10px" /></p><P><B>Capacity management</B>: Gold nanoparticle (AuNP) spacers have been used to increase the capacitance of electrochemically reduced graphene (ER-GO) to values of approximately 174 F g<SUP>&minus;1</SUP>. By the careful and systematic optimization of nanospacers loadings, the capacitance can be dramatically enhanced because these spacers prevent the graphene sheets from stacking (see picture: yellow=AuNP, green=purple=ER-GO).</P><p>[Full Paper]<br />Lucia Buglione, Alessandra Bonanni, Adriano Ambrosi, Martin Pumera<br /><i>ChemPlusChem</i> <b>2012</b>, <i>77</i>, No. 1, 71. <a href="http://dx.doi.org/10.1002/cplu.201100016">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cplu.201100026">
<title>Tuning the Release of Anticancer Drugs from Magnetic Iron Oxide/Mesoporous Silica Core/Shell Nanoparticles </title>
<link>http://dx.doi.org/10.1002/cplu.201100026</link>
<dc:creator>Nikola &#x17D;. Kne&#x17E;evi&#x107;, Igor I. Slowing, Victor S.-Y. Lin</dc:creator>
<dc:date>2011-12-16T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/cplu.201100026.gif" alt="Tuning the Release of Anticancer Drugs from Magnetic Iron Oxide/Mesoporous Silica Core/Shell Nanoparticles " style="float:left; padding-right: 10px" /></p><P><B>A series of core/shell magnetic</B> mesoporous silica nanoparticle (MMSN) materials were prepared. The loading and release of anticancer drugs, 9-aminoacridine (9AA) and camptothecin (CPT), as well as cytotoxic activity of drug loaded materials, is influenced by the presence of phenylethyl functionalization inside the MMSN mesopores (see figure). An externally applied magnetic field accelerates the drug release from the materials.</P><p>[Full Paper]<br />Nikola &#x017D;. Kne&#x017E;evi&#x0107;, Igor I. Slowing, Victor S.-Y. Lin<br /><i>ChemPlusChem</i> <b>2012</b>, <i>77</i>, No. 1, 48. <a href="http://dx.doi.org/10.1002/cplu.201100026">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cssc.201100276">
<title>Nitrogen-Doped Carbon Nanotubes as a Highly Active Metal-Free Catalyst for Selective Oxidation</title>
<link>http://dx.doi.org/10.1002/cssc.201100276</link>
<dc:creator>Kambiz Chizari, Adrien Deneuve, Ovidiu Ersen, Ileana Florea, Yu Liu, David Edouard, Izabela Janowska, Dominique Begin, Cuong Pham-Huu</dc:creator>
<dc:date>2011-12-01T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/cssc.201100276.gif" alt="Nitrogen-Doped Carbon Nanotubes as a Highly Active Metal-Free Catalyst for Selective Oxidation" style="float:left; padding-right: 10px" /></p><P><B>Nanotubes say goodbye to H</B><sub><B>2</B></sub><B>S:</B> Nitrogen-doped carbon nanotubes (N-CNTs) are synthesized by using a chemical vapor deposition method under a mixture of C<sub>2</sub>H<sub>6</sub>/NH<sub>3</sub>/Ar with Fe/Al<sub>2</sub>O<sub>3</sub> as a growth catalyst. N-CNTs can be used as a metal-free catalyst for the selective oxidation of H<sub>2</sub>S into elemental sulfur. The desulfurization activity can be further improved by supporting the N-CNT on a macroscopic host structure such as SiC foam.</P><p>[Full Paper]<br />Kambiz Chizari, Adrien Deneuve, Ovidiu Ersen, Ileana Florea, Yu Liu, David Edouard, Izabela Janowska, Dominique Begin, Cuong Pham-Huu<br /><i>ChemSusChem</i> <b>2012</b>, <i>5</i>, No. 1, 102. <a href="http://dx.doi.org/10.1002/cssc.201100276">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cssc.201100281">
<title>Hydrogen Evolution from Water/Alcohol Mixtures: Effective In Situ Generation of an Active Au/TiO&#x3C;sub&#x3E;2&#x3C;/sub&#x3E; catalyst</title>
<link>http://dx.doi.org/10.1002/cssc.201100281</link>
<dc:creator>Felix G&#xE4;rtner, Sebastian Losse, Albert Boddien, Marga-Martina Pohl, Stefania Denurra, Henrik Junge, Matthias Beller</dc:creator>
<dc:date>2011-10-27T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/cssc.201100281.gif" alt="Hydrogen Evolution from Water/Alcohol Mixtures: Effective In Situ Generation of an Active Au/TiO2 catalyst" style="float:left; padding-right: 10px" /></p><P><B>Gold standard:</B> Au/TiO<sub>2</sub> catalysts, easily prepared in situ from different Au precursors and TiO<sub>2</sub>, generate hydrogen from water/alcohol mixtures. Different alcohols, and even glucose, can serve as sacrificial reductants. The best system produces hydrogen on a liter scale, and is stable for more than two days. Deuteration studies show that proton reduction is likely the rate-limiting step in this reaction.</P><p>[Communication]<br />Felix G&auml;rtner, Sebastian Losse, Albert Boddien, Marga-Martina Pohl, Stefania Denurra, Henrik Junge, Matthias Beller<br /><i>ChemSusChem</i>, October 27, 2011, DOI: 10.1002/cssc.201100281. <a href="http://dx.doi.org/10.1002/cssc.201100281">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cssc.201100398">
<title>Renewable Rigid Diamines: Efficient, Stereospecific Synthesis of High Purity Isohexide Diamines</title>
<link>http://dx.doi.org/10.1002/cssc.201100398</link>
<dc:creator>Shanmugam Thiyagarajan, Linda Gootjes, Willem Vogelzang, Jacco van Haveren, Martin Lutz, Daan S. van Es</dc:creator>
<dc:date>2011-11-25T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/cssc.201100398.gif" alt="Renewable Rigid Diamines: Efficient, Stereospecific Synthesis of High Purity Isohexide Diamines" style="float:left; padding-right: 10px" /></p><P><B>Turning up the stereo:</B> An efficient three-step strategy for synthesizing chiral biobased dideoxy-diamino isoidide and dideoxy-diamino isosorbide in high yield with absolute stereo control is described. These highly interesting chiral building blocks are presently the subject of several investigations due to their application in high-performance biobased polymers such as polyamides and polyurethanes.</P><p>[Full Paper]<br />Shanmugam Thiyagarajan, Linda Gootjes, Willem Vogelzang, Jacco van Haveren, Martin Lutz, Daan S. van Es<br /><i>ChemSusChem</i> <b>2011</b>, <i>4</i>, No. 12, 1823. <a href="http://dx.doi.org/10.1002/cssc.201100398">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cssc.201100492">
<title>Synthesis of Cyclic Sulfites from Epoxides and Sulfur Dioxide with Silica-Immobilized Homogeneous Catalysts</title>
<link>http://dx.doi.org/10.1002/cssc.201100492</link>
<dc:creator>Yasumasa Takenaka, Takahiro Kiyosu, Goro Mori, Jun-Chul Choi, Norihisa Fukaya, Toshiyasu Sakakura, Hiroyuki Yasuda</dc:creator>
<dc:date>2011-12-01T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/cssc.201100492.gif" alt="Synthesis of Cyclic Sulfites from Epoxides and Sulfur Dioxide with Silica-Immobilized Homogeneous Catalysts" style="float:left; padding-right: 10px" /></p><P><B>Immobilized for crimes of pyrolysis:</B> Quaternary ammonium- and amino-functionalized silica catalysts promote the cycloaddition of sulfur dioxide to epoxides to produce cyclic sulfites in high yields (79&ndash;96 %) that are comparable to those with the homogeneous catalysts. Separation of the functionalized silica catalyst from the product solution by filtration avoids pyrolysis of the cyclic sulfites during purification by distillation.</P><p>[Full Paper]<br />Yasumasa Takenaka, Takahiro Kiyosu, Goro Mori, Jun-Chul Choi, Norihisa Fukaya, Toshiyasu Sakakura, Hiroyuki Yasuda<br /><i>ChemSusChem</i> <b>2012</b>, <i>5</i>, No. 1, 194. <a href="http://dx.doi.org/10.1002/cssc.201100492">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201100700">
<title>Heterometallic Oximato-Bridged Linear Trinuclear Ni&#x3C;SUP&#x3E;II&#x3C;/SUP&#x3E;&#x2212;M&#x3C;SUP&#x3E;III&#x3C;/SUP&#x3E;&#x2212;Ni&#x3C;SUP&#x3E;II&#x3C;/SUP&#x3E; (M&#x3C;SUP&#x3E;III&#x3C;/SUP&#x3E; = Mn, Fe, Tb) Complexes Constructed with the &#x3C;I&#x3E;fac&#x3C;/I&#x3E;-O&#x3C;sub&#x3E;3&#x3C;/sub&#x3E; [Ni(HL)&#x3C;sub&#x3E;3&#x3C;/sub&#x3E;]&#x3C;SUP&#x3E;&#x2013;&#x3C;/SUP&#x3E; Metalloligand (H&#x3C;sub&#x3E;2&#x3C;/sub&#x3E;L = pyrimidine-2-carboxamide oxime): A Theoretical and Experimental Magneto-Structural Study</title>
<link>http://dx.doi.org/10.1002/ejic.201100700</link>
<dc:creator>Cerise Kalogridis, Mar&#xED;a A. Palacios, Antonio Rodr&#xED;guez-Di&#xE9;guez, Antonio J. Mota, Duane Choquesillo-Lazarte, Euan K. Brechin, Enrique Colacio</dc:creator>
<dc:date>2011-11-04T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/ejic.201100700.jpg" alt="Heterometallic Oximato-Bridged Linear Trinuclear NiII&minus;MIII&minus;NiII (MIII = Mn, Fe, Tb) Complexes Constructed with the fac-O3 [Ni(HL)3]&ndash; Metalloligand (H2L = pyrimidine-2-carboxamide oxime): A Theoretical and Experimental Magneto-Structural Study" style="float:left; padding-right: 10px" /></p><P>Three oximato-bridged linear heterobimetallic complexes [NiMNi] (M = Mn<SUP>3+</SUP>, Fe<SUP>3+</SUP>, Tb<SUP>3+</SUP>) have been prepared using [Ni(HL)]<SUP>&ndash;</SUP> (H<sub>2</sub>L = pyrimidine-2-carboxamide oxime). The size of the antiferromagnetic interactions in the Mn<SUP>3+</SUP> and Fe<SUP>3+</SUP> complexes has been supported by DFT calculations and justified on based on structural parameters, e.g. the Ni&ndash;N&ndash;O&ndash;M torsional angle and the distortion from the OC-6 octahedral to the TPR-6 trigonal prismatic geometry.</P><p>[Full Paper]<br />Cerise Kalogridis, Mar&iacute;a A. Palacios, Antonio Rodr&iacute;guez-Di&eacute;guez, Antonio J. Mota, Duane Choquesillo-Lazarte, Euan K. Brechin, Enrique Colacio<br /><i>Eur. J. Inorg. Chem.</i> <b>2011</b>, No. 34, 5225. <a href="http://dx.doi.org/10.1002/ejic.201100700">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201100834">
<title>Dyes That Bear Thiazolylazo Groups as Chromogenic Chemosensors for Metal Cations</title>
<link>http://dx.doi.org/10.1002/ejic.201100834</link>
<dc:creator>Tatiana Abalos, Mar&#xED;a Moragues, Santiago Royo, Diego Jim&#xE9;nez, Ram&#xF3;n Mart&#xED;nez-M&#xE1;&#xF1;ez, Juan Soto, F&#xE9;lix Sancen&#xF3;n, Salvador Gil, Joan Cano</dc:creator>
<dc:date>2011-11-22T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/ejic.201100834.jpg" alt="Dyes That Bear Thiazolylazo Groups as Chromogenic Chemosensors for Metal Cations" style="float:left; padding-right: 10px" /></p><P>A family of dyes that contain a thiazolylazo group and several macrocyclic cavities with different ring sizes and type and number of heteroatoms has been synthesised and characterized. Studies of protonation and coordination behaviour in the presence of metal cations have been carried out. The interaction was also studied by using density functional theory quantum mechanical calculations.</P><p>[Full Paper]<br />Tatiana Abalos, Mar&iacute;a Moragues, Santiago Royo, Diego Jim&eacute;nez, Ram&oacute;n Mart&iacute;nez-M&aacute;&ntilde;ez, Juan Soto, F&eacute;lix Sancen&oacute;n, Salvador Gil, Joan Cano<br /><i>Eur. J. Inorg. Chem.</i> <b>2012</b>, No. 1, 76. <a href="http://dx.doi.org/10.1002/ejic.201100834">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201100890">
<title>Hydroalumination of Bis(alkynyl)silanes: Generation of Chelating Lewis Acids, Their Application in the Coordination of Chloride Ions and a 1,1-Carbalumination Reaction</title>
<link>http://dx.doi.org/10.1002/ejic.201100890</link>
<dc:creator>Werner Uhl, Denis Heller, Jutta K&#xF6;sters, Ernst-Ulrich W&#xFC;rthwein, Nugzar Ghavtadze</dc:creator>
<dc:date>2011-11-07T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/ejic.201100890.jpg" alt="Hydroalumination of Bis(alkynyl)silanes: Generation of Chelating Lewis Acids, Their Application in the Coordination of Chloride Ions and a 1,1-Carbalumination Reaction" style="float:left; padding-right: 10px" /></p><P>Chelating Lewis acids containing two coordinatively unsaturated, tricoordinate aluminium atoms were obtained from a facile route by the twofold hydroalumination of dialkynylsilanes. An intermediately formed alkenyl&ndash;alkynylsilane gave a silacyclobutene derivative by 1,1-carbalumination.</P><p>[Full Paper]<br />Werner Uhl, Denis Heller, Jutta K&ouml;sters, Ernst-Ulrich W&uuml;rthwein, Nugzar Ghavtadze<br /><i>Eur. J. Inorg. Chem.</i>, November 7, 2011, DOI: 10.1002/ejic.201100890. <a href="http://dx.doi.org/10.1002/ejic.201100890">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201100894">
<title>Lanthanide Complexes as Paramagnetic Probes for &#x3C;SUP&#x3E;19&#x3C;/SUP&#x3E;F Magnetic Resonance</title>
<link>http://dx.doi.org/10.1002/ejic.201100894</link>
<dc:creator>Peter Harvey, Ilya Kuprov, David Parker</dc:creator>
<dc:date>2011-11-08T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/ejic.201100894.jpg" alt="Lanthanide Complexes as Paramagnetic Probes for 19F Magnetic Resonance" style="float:left; padding-right: 10px" /></p><P>Sensitivity in <SUP>19</SUP>F magnetic resonance spectroscopy and imaging is enhanced by placing a paramagnetic lanthanide within 7 &Aring; of the spin label. Faster relaxation allows more rapid data acquisition for systems generating one main resonance, and the proximate lanthanide ion amplifies the chemical shift non-equivalence in responsive probes.</P><p>[Microreview]<br />Peter Harvey, Ilya Kuprov, David Parker<br /><i>Eur. J. Inorg. Chem.</i>, November 8, 2011, DOI: 10.1002/ejic.201100894. <a href="http://dx.doi.org/10.1002/ejic.201100894">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101057">
<title>Orthogonal Protecting Groups in the Synthesis of Tryptophanyl-Hexahydropyrroloindoles</title>
<link>http://dx.doi.org/10.1002/ejoc.201101057</link>
<dc:creator>Pau Ruiz-Sanchis, Svetlana A. Savina, Gerardo A. Acosta, Fernando Albericio, Mercedes Alvarez</dc:creator>
<dc:date>2011-11-22T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/ejoc.201101057.jpg" alt="Orthogonal Protecting Groups in the Synthesis of Tryptophanyl-Hexahydropyrroloindoles" style="float:left; padding-right: 10px" /></p><P>Several tryptophanyl-hexahydropyrroloindoles (Trp-HPI) with four or five orthogonal protecting groups have been synthesized. This polyheterocyclic system constitutes a scaffold for many natural products that have recently been isolated.</P><p>[Full Paper]<br />Pau Ruiz-Sanchis, Svetlana A. Savina, Gerardo A. Acosta, Fernando Albericio, Mercedes Alvarez<br /><i>Eur. J. Org. Chem.</i> <b>2012</b>, No. 1, 67. <a href="http://dx.doi.org/10.1002/ejoc.201101057">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101215">
<title>Coloured Artefacts Formed by Oxidation of Benzene-1,2,4-triol and &#x3B2;-Dopa During the Extraction of &#x3C;I&#x3E;Cortinarius violaceus&#x3C;/I&#x3E; (Agaricales) with Alcohols
</title>
<link>http://dx.doi.org/10.1002/ejoc.201101215</link>
<dc:creator>Franz von Nussbaum, Matthias R&#xFC;th, Peter Spiteller, Tina H&#xFC;bscher-Weissert, Florian L&#xF6;bermann, Kurt Polborn, Wolfgang Steglich</dc:creator>
<dc:date>2011-11-09T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/ejoc.201101215.jpg" alt="Coloured Artefacts Formed by Oxidation of Benzene-1,2,4-triol and &beta;-Dopa During the Extraction of Cortinarius violaceus (Agaricales) with Alcohols
" style="float:left; padding-right: 10px" /></p><P>Extraction of the mushroom <I>Cortinarius violaceus</I> with methanol leads to the formation of several colourful artefacts. They arise from benzene-1,2,4-triol, &beta;-dopa, and iron(III) ions, all of which are present in the fungus.</P><p>[Full Paper]<br />Franz von Nussbaum, Matthias R&uuml;th, Peter Spiteller, Tina H&uuml;bscher-Weissert, Florian L&ouml;bermann, Kurt Polborn, Wolfgang Steglich<br /><i>Eur. J. Org. Chem.</i> <b>2012</b>, No. 2, 380. <a href="http://dx.doi.org/10.1002/ejoc.201101215">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101249">
<title>Hydrophobic Vitamin B&#x3C;sub&#x3E;12&#x3C;/sub&#x3E; Derivatives: Unprecedented Formation of a 7-Membered Lactam</title>
<link>http://dx.doi.org/10.1002/ejoc.201101249</link>
<dc:creator>Keith &#xF3; Proinsias, Sylwester Kurco&#x144;, Dorota Gryko</dc:creator>
<dc:date>2011-11-10T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/ejoc.201101249.jpg" alt="Hydrophobic Vitamin B12 Derivatives: Unprecedented Formation of a 7-Membered Lactam" style="float:left; padding-right: 10px" /></p><P>Synthesis of a seven-membered lactam&ndash;cobalamin derivative was achieved through intramolecular acidic aminolysis of heptamethyl dicyanocobyrinate with the NH<sub>2</sub> group at the C10 position. Subsequent ring opening gave new C8,C10-diamides.</P><p>[Full Paper]<br />Keith &oacute; Proinsias, Sylwester Kurco&#x0144;, Dorota Gryko<br /><i>Eur. J. Org. Chem.</i> <b>2012</b>, No. 1, 154. <a href="http://dx.doi.org/10.1002/ejoc.201101249">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201101284">
<title>Substituted Functional Olefins Through Lateral Sequential Lithiation/Silylation/Condensation of Tertiary Aromatic Amides: A Ligand for Phosphane-Free Palladium-Catalyzed Suzuki Coupling Reactions</title>
<link>http://dx.doi.org/10.1002/ejoc.201101284</link>
<dc:creator>Li-Wen Xu, Xi-Huai Chen, Hao Shen, Yuan Deng, Jian-Xiong Jiang, Kezhi Jiang, Guo-Qiao Lai, Chun-Qi Sheng</dc:creator>
<dc:date>2011-11-09T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/ejoc.201101284.jpg" alt="Substituted Functional Olefins Through Lateral Sequential Lithiation/Silylation/Condensation of Tertiary Aromatic Amides: A Ligand for Phosphane-Free Palladium-Catalyzed Suzuki Coupling Reactions" style="float:left; padding-right: 10px" /></p><P>A new type of olefin was prepared by an unprecedented lateral sequential lithiation/silylation/condensation of tertiary aromatic amides in good yield. The resulting functional olefin, containing an amide moiety, could act as an efficient ligand in phosphane-free palladium-catalyzed Suzuki cross-coupling reactions.</P><p>[Full Paper]<br />Li-Wen Xu, Xi-Huai Chen, Hao Shen, Yuan Deng, Jian-Xiong Jiang, Kezhi Jiang, Guo-Qiao Lai, Chun-Qi Sheng<br /><i>Eur. J. Org. Chem.</i> <b>2012</b>, No. 2, 290. <a href="http://dx.doi.org/10.1002/ejoc.201101284">Read article.</a></p> ]]></content:encoded>
</item>
</rdf:RDF>
