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<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>2013-05-24T19:38:31Z</dc:date>
<dc:publisher>Wiley-VCH</dc:publisher>
<dc:creator>mmueller@wiley-vch.de</dc:creator>
<dc:subject>Chemistry</dc:subject>
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<item rdf:about="http://dx.doi.org/10.1002/ajoc.201200201">
<title>Synthesis and Optical Properties of Tetraaryl-1,4-dihydropyrrolo[3,2-&#x3C;I&#x3E;b&#x3C;/I&#x3E;]pyrroles</title>
<link>http://dx.doi.org/10.1002/ajoc.201200201</link>
<dc:creator>Anita Janiga, Eliza Glodkowska-Mrowka, Tomasz Stoklosa, Daniel T. Gryko</dc:creator>
<dc:date>2013-02-18T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/ajoc.201200201.gif" alt="Synthesis and Optical Properties of Tetraaryl-1,4-dihydropyrrolo[3,2-b]pyrroles" style="float:left; padding-right: 10px" /></p><P><B>Hit for six!</B> Six bonds are formed in a tandem process that gives rise to substituted 1,4-dihydropyrrole[3,2-<I>b</I>]pyrroles. Unparalleled simplicity and versatility of this one-pot reaction, no chromatography, as well as highly interesting optical properties have the potential to bring these molecules to the forefront in various applications.</P><p>[Full Paper]<br />Anita Janiga, Eliza Glodkowska-Mrowka, Tomasz Stoklosa, Daniel T. Gryko<br /><i>Asian J. Org. Chem.</i> <b>2013</b>, <i>2</i>, No. 5, 411. <a href="http://dx.doi.org/10.1002/ajoc.201200201">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ajoc.201200203">
<title>The Origin of the Emission Properties of &#x3C0;-Conjugated Molecules that have an Acid-responsive Benzimidazole Unit</title>
<link>http://dx.doi.org/10.1002/ajoc.201200203</link>
<dc:creator>Toshifumi Inouchi, Takuya Nakashima, Tsuyoshi Kawai</dc:creator>
<dc:date>2013-03-01T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/ajoc.201200203.gif" alt="The Origin of the Emission Properties of &pi;-Conjugated Molecules that have an Acid-responsive Benzimidazole Unit" style="float:left; padding-right: 10px" /></p><P><B>A twist in the tale</B>: The emission properties of &pi;-conjugated molecules with an <I>N</I>-methylbenzimidazole as a proton-responsive unit are compared between T-shaped cross-conjugated and linear conjugated molecules. Acid-responsive twisted intramolecular charge-transfer (TICT) emission requires the cross-conjugated T-shaped structure in terms of the separation of frontier molecular orbitals of the HOMO and LUMO, as well as bond rotation.</P><p>[Full Paper]<br />Toshifumi Inouchi, Takuya Nakashima, Tsuyoshi Kawai<br /><i>Asian J. Org. Chem.</i> <b>2013</b>, <i>2</i>, No. 3, 230. <a href="http://dx.doi.org/10.1002/ajoc.201200203">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ajoc.201300007">
<title>Application of Tertiary Amines Synthesized by Catalytic Dehydrogenation of Enamines as Nucleophilic C&#x3C;sub&#x3E;2&#x3C;/sub&#x3E; Synthons for 1,4-Conjugate Addition with Fluoroalkylated Olefins</title>
<link>http://dx.doi.org/10.1002/ajoc.201300007</link>
<dc:creator>Atsunori Morigaki, Mio Kawamura, Satoru Arimitsu, Takashi Ishihara, Tsutomu Konno</dc:creator>
<dc:date>2013-02-11T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/ajoc.201300007.gif" alt="Application of Tertiary Amines Synthesized by Catalytic Dehydrogenation of Enamines as Nucleophilic C2 Synthons for 1,4-Conjugate Addition with Fluoroalkylated Olefins" style="float:left; padding-right: 10px" /></p><P><B>The synthesis</B> of enamines from only tertiary amines has been developed by using a catalytic amount of Pd(OAc)<sub>2</sub> (5 mol %) in air. These generated enamines were successfully used for 1,4-conjugated addition reactions with fluoroalkylated olefins as an alternative synthetic route for the formylmethylation of olefins. This reaction adds potential for the use of tertiary amines as a nucleophilic C<sub>2</sub> synthon. EWG=electron-withdrawing group.</P><p>[Full Paper]<br />Atsunori Morigaki, Mio Kawamura, Satoru Arimitsu, Takashi Ishihara, Tsutomu Konno<br /><i>Asian J. Org. Chem.</i> <b>2013</b>, <i>2</i>, No. 3, 239. <a href="http://dx.doi.org/10.1002/ajoc.201300007">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ajoc.201300017">
<title>The Addition of ArSSAr to Alkenes: The Implications of a Cationic Chain Mechanism Initiated by Electrogenerated ArS(ArSSAr)&#x3C;SUP&#x3E;+&#x3C;/SUP&#x3E;</title>
<link>http://dx.doi.org/10.1002/ajoc.201300017</link>
<dc:creator>Kouichi Matsumoto, Tomonari Sanada, Hayato Shimazaki, Kazuaki Shimada, Shino Hagiwara, Shunsuke Fujie, Yosuke Ashikari, Seiji Suga, Shigenori Kashimura, Jun-ichi Yoshida</dc:creator>
<dc:date>2013-03-21T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/ajoc.201300017.gif" alt="The Addition of ArSSAr to Alkenes: The Implications of a Cationic Chain Mechanism Initiated by Electrogenerated ArS(ArSSAr)+" style="float:left; padding-right: 10px" /></p><P><B>She's electric</B>: The addition reactions of diaryl disulfides (ArSSAr) to alkenes and alkynes were achieved with a catalytic amount of an electrochemically generated arylbis(arylthio)sulfonium ion (ArS(ArSSAr)<SUP>+</SUP>) to give the corresponding diarylthiolated products. A cation chain mechanism mediated by ArS(ArSSAr)<SUP>+</SUP> as a chain carrier is suggested.</P><p>[Full Paper]<br />Kouichi Matsumoto, Tomonari Sanada, Hayato Shimazaki, Kazuaki Shimada, Shino Hagiwara, Shunsuke Fujie, Yosuke Ashikari, Seiji Suga, Shigenori Kashimura, Jun-ichi Yoshida<br /><i>Asian J. Org. Chem.</i> <b>2013</b>, <i>2</i>, No. 4, 325. <a href="http://dx.doi.org/10.1002/ajoc.201300017">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/anie.201210329">
<title>Calcite Crystal Growth by a Solid-State Transformation of Stabilized Amorphous Calcium Carbonate Nanospheres in a Hydrogel
</title>
<link>http://dx.doi.org/10.1002/anie.201210329</link>
<dc:creator>Assaf Gal, Wouter Habraken, Dvir Gur, Peter Fratzl, Steve Weiner, Lia Addadi</dc:creator>
<dc:date>2013-04-04T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/anie.201210329.gif" alt="Calcite Crystal Growth by a Solid-State Transformation of Stabilized Amorphous Calcium Carbonate Nanospheres in a Hydrogel
" style="float:left; padding-right: 10px" /></p><P><B>An ugly duckling grows into a swan</B>: Many organisms grow their crystalline mineral phases through the secondary nucleation of nanospheres made of an amorphous precursor phase. Stable amorphous calcium carbonate biominerals were used to induce a similar transformation in vitro. The amorphous nanospheres underwent a solid-phase transformation that resulted in highly ordered calcite crystals composed of aggregated particles (see SEM image).</P><p>[Communication]<br />Assaf Gal, Wouter Habraken, Dvir Gur, Peter Fratzl, Steve Weiner, Lia Addadi<br /><i>Angew. Chem. Int. Ed.</i> <b>2013</b>, <i>52</i>, No. 18, 4867. <a href="http://dx.doi.org/10.1002/anie.201210329">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/anie.201210359">
<title>A Plasmon-Assisted Optofluidic (PAOF) System for Measuring the Photothermal Conversion Efficiencies of Gold Nanostructures and Controlling an Electrical Switch
</title>
<link>http://dx.doi.org/10.1002/anie.201210359</link>
<dc:creator>Jie Zeng, David Goldfeld, Younan Xia</dc:creator>
<dc:date>2013-03-12T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/anie.201210359.gif" alt="A Plasmon-Assisted Optofluidic (PAOF) System for Measuring the Photothermal Conversion Efficiencies of Gold Nanostructures and Controlling an Electrical Switch
" style="float:left; padding-right: 10px" /></p><P><B>&ldquo;Photothermometer&rdquo;</B>: A PAOF system was constructed using a diode laser as the energy source, an aqueous suspension of plasmonic nanostructures as the photothermal transducer, and a glass capillary for measuring the volumetric expansion of the suspension (see picture). The suspension could be driven to move up the capillary by more than 30 mm and be used to control the operation of an electrical switch.</P><p>[Communication]<br />Jie Zeng, David Goldfeld, Younan Xia<br /><i>Angew. Chem. Int. Ed.</i> <b>2013</b>, <i>52</i>, No. 15, 4169. <a href="http://dx.doi.org/10.1002/anie.201210359">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/anie.201300751">
<title>Interactions of a Periplasmic Binding Protein with a Tetradentate Siderophore Mimic
</title>
<link>http://dx.doi.org/10.1002/anie.201300751</link>
<dc:creator>Daniel J. Raines, Olga V. Moroz, Keith S. Wilson, Anne-K. Duhme-Klair</dc:creator>
<dc:date>2013-03-19T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/anie.201300751.gif" alt="Interactions of a Periplasmic Binding Protein with a Tetradentate Siderophore Mimic
" style="float:left; padding-right: 10px" /></p><P><B>Iron-bound structure</B>: The ferric complex of a tetradentate siderophore mimic was synthesized and co-crystallized with the periplasmic binding protein CeuE of <I>Campylobacter jejuni.</I> In addition to electrostatic and hydrogen-bonding interactions between the binding pocket and the substrate, the structure showed direct coordination of two amino acid side chains to the Fe<SUP>III</SUP> center (orange, see figure).</P><p>[Communication]<br />Daniel J. Raines, Olga V. Moroz, Keith S. Wilson, Anne-K. Duhme-Klair<br /><i>Angew. Chem. Int. Ed.</i> <b>2013</b>, <i>52</i>, No. 17, 4595. <a href="http://dx.doi.org/10.1002/anie.201300751">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/anie.201301128">
<title>A Gel-Based Trihybrid System Containing Nanofibers, Nanosheets, and Nanoparticles: Modulation of the Rheological Property and Catalysis
</title>
<link>http://dx.doi.org/10.1002/anie.201301128</link>
<dc:creator>Jayanta Nanda, Abhijit Biswas, Bimalendu Adhikari, Arindam Banerjee</dc:creator>
<dc:date>2013-04-08T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/anie.201301128.gif" alt="A Gel-Based Trihybrid System Containing Nanofibers, Nanosheets, and Nanoparticles: Modulation of the Rheological Property and Catalysis
" style="float:left; padding-right: 10px" /></p><P><B>Wonderful gels</B>: A trihybrid gel was prepared by incorporating graphene oxide and in situ synthesized gold nanoparticles (AuNPs) into an amino-acid-based native gel matrix (see pict). The morphology of this system indicates the presence of three distinctly different nanostructures: nanofibers, nanosheets, and nanoparticles. The catalytic efficiency of this trihybrid system is enhanced relative to that of AuNPs in a dihybrid system.</P><p>[Communication]<br />Jayanta Nanda, Abhijit Biswas, Bimalendu Adhikari, Arindam Banerjee<br /><i>Angew. Chem. Int. Ed.</i> <b>2013</b>, <i>52</i>, No. 19, 5041. <a href="http://dx.doi.org/10.1002/anie.201301128">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/asia.201201060">
<title>Unusual Binding of a Potential Biomarker with Human Serum Albumin</title>
<link>http://dx.doi.org/10.1002/asia.201201060</link>
<dc:creator>Dipanwita De, Harpreet Kaur, Anindya Datta</dc:creator>
<dc:date>2013-02-12T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/asia.201201060.gif" alt="Unusual Binding of a Potential Biomarker with Human Serum Albumin" style="float:left; padding-right: 10px" /></p><P><B>Ties that bind</B>: Typically, a fluorophore binds to one of the Sudlow's sites on albumin. Surprisingly, BP(OH)<sub>2</sub> did not exhibit such behavior, but rather appeared to bind to a cleft at the interface of subdomains IIIA and IIB.</P><p>[Full Paper]<br />Dipanwita De, Harpreet Kaur, Anindya Datta<br /><i>Chem. Asian J.</i> <b>2013</b>, <i>8</i>, No. 4, 728. <a href="http://dx.doi.org/10.1002/asia.201201060">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/asia.201201109">
<title>Formation of Nanostructured MnO/Co/Solid&#x2013;Electrolyte Interphase Ternary Composites as a Durable Anode Material for Lithium-Ion Batteries</title>
<link>http://dx.doi.org/10.1002/asia.201201109</link>
<dc:creator>Feng Dang, Yuya Oaki, Takao Kokubu, Eiji Hosono, Haoshen Zhou, Hiroaki Imai</dc:creator>
<dc:date>2013-02-07T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/asia.201201109.gif" alt="Formation of Nanostructured MnO/Co/Solid&ndash;Electrolyte Interphase Ternary Composites as a Durable Anode Material for Lithium-Ion Batteries" style="float:left; padding-right: 10px" /></p><P><B>An ode to anodes</B>: Ternary nanocomposites consisting of a porous MnO framework, metallic Co nanoparticles, and a solid&ndash;electrolyte interphase (SEI) were produced from MnCO<sub>3</sub> precursors. As the highly dispersed Co nanoparticles and SEI provide electron and Li-ion conductive networks, respectively, the MnO frameworks are applicable as durable anode materials for Li-ion batteries.</P><p>[Full Paper]<br />Feng Dang, Yuya Oaki, Takao Kokubu, Eiji Hosono, Haoshen Zhou, Hiroaki Imai<br /><i>Chem. Asian J.</i> <b>2013</b>, <i>8</i>, No. 4, 760. <a href="http://dx.doi.org/10.1002/asia.201201109">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/asia.201201227">
<title>1,2-Bis(ferrocenyl)-Substituted Distibene and Dibismuthene: Sb=Sb and Bi=Bi Units as &#x3C0; Spacers between Two Ferrocenyl Units</title>
<link>http://dx.doi.org/10.1002/asia.201201227</link>
<dc:creator>Michiyasu Sakagami, Takahiro Sasamori, Heisuke Sakai, Yukio Furukawa, Norihiro Tokitoh</dc:creator>
<dc:date>2013-02-01T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/asia.201201227.gif" alt="1,2-Bis(ferrocenyl)-Substituted Distibene and Dibismuthene: Sb=Sb and Bi=Bi Units as &pi; Spacers between Two Ferrocenyl Units" style="float:left; padding-right: 10px" /></p><P><B>Pi in the sky</B>: 1,2-bis(ferrocenyl)distibene and 1,2-bis(ferrocenyl)dibismuthene derivatives, where two bulky ferrocenyl units are bridged by a Sb=Sb and Bi=Bi &pi; spacer, have been synthesized as a new family of novel d&ndash;&pi; conjugated systems. Their molecular structures, spectroscopic behavior, and electrochemical properties reveal the Sb=Sb and Bi=Bi units to be effective &pi;-electron spacers.</P><p>[Communication]<br />Michiyasu Sakagami, Takahiro Sasamori, Heisuke Sakai, Yukio Furukawa, Norihiro Tokitoh<br /><i>Chem. Asian J.</i> <b>2013</b>, <i>8</i>, No. 4, 690. <a href="http://dx.doi.org/10.1002/asia.201201227">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/asia.201300003">
<title>Redox Inactive Metal Ion Promoted C-H Activation of Benzene to Phenol with Pd&#x3C;SUP&#x3E;II&#x3C;/SUP&#x3E;(bpym): Demonstrating New Strategies in Catalyst Designs</title>
<link>http://dx.doi.org/10.1002/asia.201300003</link>
<dc:creator>Huajun Guo, Zhuqi Chen, Fuming Mei, Dajian Zhu, Hui Xiong, Guochuan Yin</dc:creator>
<dc:date>2013-02-10T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/asia.201300003.gif" alt="Redox Inactive Metal Ion Promoted C-H Activation of Benzene to Phenol with PdII(bpym): Demonstrating New Strategies in Catalyst Designs" style="float:left; padding-right: 10px" /></p><P><B>Al in</B>: A new strategy was introduced to modify the electronics and steric hindrance of the Pd<SUP>II</SUP> ion in order to change its reactivity towards benzene hydroxylation. In trifluoroacetic acid, free Pd<SUP>II</SUP> ions provide dominantly biphenyl, with phenol as minor product. Ligation of bpym to the Pd<SUP>II</SUP> ion results in its deactivation with regard to benzene functionalization. The addition of the redox inactive Al<SUP>III</SUP> ion to the Pd<SUP>II</SUP>(bpym) complex recovers its catalytic activity, and alters the reactivity of Pd<SUP>II</SUP> ion from benzene coupling to hydroxylation.</P><p>[Communication]<br />Huajun Guo, Zhuqi Chen, Fuming Mei, Dajian Zhu, Hui Xiong, Guochuan Yin<br /><i>Chem. Asian J.</i> <b>2013</b>, <i>8</i>, No. 5, 888. <a href="http://dx.doi.org/10.1002/asia.201300003">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cbic.201200714">
<title>Structural Insights into the Recovery of Aldolase Activity in &#x3C;I&#x3E;N&#x3C;/I&#x3E;-Acetylneuraminic Acid Lyase by Replacement of the Catalytically Active Lysine with &#x3B3;-Thialysine by Using a Chemical Mutagenesis Strategy</title>
<link>http://dx.doi.org/10.1002/cbic.201200714</link>
<dc:creator>Nicole Timms, Claire L. Windle, Anna Polyakova, James R. Ault, Chi H. Trinh, Arwen R. Pearson, Adam Nelson, Alan Berry</dc:creator>
<dc:date>2013-02-18T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/cbic.201200714.gif" alt="Structural Insights into the Recovery of Aldolase Activity in N-Acetylneuraminic Acid Lyase by Replacement of the Catalytically Active Lysine with &gamma;-Thialysine by Using a Chemical Mutagenesis Strategy" style="float:left; padding-right: 10px" /></p><P><B>Looks like lysine:</B> The catalytically essential lysine in <I>N</I>-acetylneuraminic acid lyase was replaced by thialysine by chemical modification. High yields of modified enzyme allowed detailed structural and kinetic analyses which demonstrated that thialysine is a good structural mimic of lysine, but that the altered p<I>K</I><sub>a</sub> of the thialysine results in lower recovery of activity.</P><p>[Full Paper]<br />Nicole Timms, Claire L. Windle, Anna Polyakova, James R. Ault, Chi H. Trinh, Arwen R. Pearson, Adam Nelson, Alan Berry<br /><i>ChemBioChem</i> <b>2013</b>, <i>14</i>, No. 4, 474. <a href="http://dx.doi.org/10.1002/cbic.201200714">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cbic.201200718">
<title>Engineering New Protein&#x2013;Protein Interactions on the &#x3B2;-Propeller Fold by Yeast Cell Surface Display</title>
<link>http://dx.doi.org/10.1002/cbic.201200718</link>
<dc:creator>Keya Zhang, Heng Li, Karan Bhuripanyo, Bo Zhao, Tiffany F. Chen, Ning Zheng, Jun Yin</dc:creator>
<dc:date>2013-02-10T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/cbic.201200718.gif" alt="Engineering New Protein&ndash;Protein Interactions on the &beta;-Propeller Fold by Yeast Cell Surface Display" style="float:left; padding-right: 10px" /></p><P><B>Reinventing the wheel</B>: The &beta;-propeller domain folds like a wheel to provide key protein&ndash;protein interactions in the cell. Here we used high-throughput yeast sorting to &ldquo;invent&rdquo; &beta;-propellers of new binding specificities with cellular targets.</P><p>[Communication]<br />Keya Zhang, Heng Li, Karan Bhuripanyo, Bo Zhao, Tiffany F. Chen, Ning Zheng, Jun Yin<br /><i>ChemBioChem</i> <b>2013</b>, <i>14</i>, No. 4, 426. <a href="http://dx.doi.org/10.1002/cbic.201200718">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cbic.201200727">
<title>Dissecting the Roles of the N- and C-Flanking Residues of Acetyllysine Substrates for SIRT1 Activity</title>
<link>http://dx.doi.org/10.1002/cbic.201200727</link>
<dc:creator>Roman Meledin, Ashraf Brik, Amir Aharoni</dc:creator>
<dc:date>2013-02-20T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/cbic.201200727.gif" alt="Dissecting the Roles of the N- and C-Flanking Residues of Acetyllysine Substrates for SIRT1 Activity" style="float:left; padding-right: 10px" /></p><P><B>SIRT1 specificity</B>: The multispecific SIRT1 enzyme catalyzes the deacetylation of acetyllysine residues within protein targets. However, little is known regarding the molecular basis for SIRT1 substrate recognition. Kinetic analysis of SIRT1 with a panel of peptide substrates shows the high importance of the region N-flanking the target acetyllysine and its high conservation through evolution.</P><p>[Communication]<br />Roman Meledin, Ashraf Brik, Amir Aharoni<br /><i>ChemBioChem</i> <b>2013</b>, <i>14</i>, No. 5, 577. <a href="http://dx.doi.org/10.1002/cbic.201200727">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cbic.201300037">
<title>An Enzymatic Route to Selenazolines</title>
<link>http://dx.doi.org/10.1002/cbic.201300037</link>
<dc:creator>Jesko Koehnke, Falk Morawitz, Andrew F. Bent, Wael E. Houssen, Sally L. Shirran, Matthew A. Fuszard, Iain A. Smellie, Catherine H. Botting, Margaret C. M. Smith, Marcel Jaspars, James H. Naismith</dc:creator>
<dc:date>2013-02-18T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/cbic.201300037.gif" alt="An Enzymatic Route to Selenazolines" style="float:left; padding-right: 10px" /></p><P><B>Ringing the changes:</B> Selenazolines have applications in medicinal chemistry, but their synthesis is challenging. We report a new convenient and less toxic route to these heterocycles that starts from commercially available selenocysteine. The new route depends on a heterocyclase enzyme that creates oxazolines and thiazolines from serines/threonines and cysteines.</P><p>[Communication]<br />Jesko Koehnke, Falk Morawitz, Andrew F. Bent, Wael E. Houssen, Sally L. Shirran, Matthew A. Fuszard, Iain A. Smellie, Catherine H. Botting, Margaret C. M. Smith, Marcel Jaspars, James H. Naismith<br /><i>ChemBioChem</i> <b>2013</b>, <i>14</i>, No. 5, 564. <a href="http://dx.doi.org/10.1002/cbic.201300037">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cctc.201200551">
<title>Efficient Tertiary Amine/Weak Acid Bifunctional Mesoporous Silica Catalysts for Michael Addition Reactions</title>
<link>http://dx.doi.org/10.1002/cctc.201200551</link>
<dc:creator>Sayantani Das, Anandarup Goswami, Nagarajan Murali, Tewodros Asefa</dc:creator>
<dc:date>2013-01-29T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/cctc.201200551.gif" alt="Efficient Tertiary Amine/Weak Acid Bifunctional Mesoporous Silica Catalysts for Michael Addition Reactions" style="float:left; padding-right: 10px" /></p><P><B>Dual activity:</B> We report the synthesis and efficient catalytic properties of acid&ndash;base bifunctional mesoporous silica catalyst comprising tertiary amine and optimized concentration of surface silanol (weak acid) groups for the Michael addition reactions between various <I>trans</I>-&beta;-nitrostyrenes and active methylene compounds, such as malononitrile, acetylacetone, and diethylmalonate.</P><p>[Full Paper]<br />Sayantani Das, Anandarup Goswami, Nagarajan Murali, Tewodros Asefa<br /><i>ChemCatChem</i> <b>2013</b>, <i>5</i>, No. 4, 910. <a href="http://dx.doi.org/10.1002/cctc.201200551">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cctc.201200591">
<title>Synergistic Catalysis over Bimetallic Alloy Nanoparticles</title>
<link>http://dx.doi.org/10.1002/cctc.201200591</link>
<dc:creator>Ashish Kumar Singh, Qiang Xu</dc:creator>
<dc:date>2013-01-23T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/cctc.201200591.gif" alt="Synergistic Catalysis over Bimetallic Alloy Nanoparticles" style="float:left; padding-right: 10px" /></p><P><B>Co-op multiplayer:</B> The synergistic effect of bimetallic alloy nanoparticles in various catalytic reactions is highlighted, in particular those related to fuel cells, such as the electrochemical oxidation of MeOH, EtOH, and formic acid, CO oxidation, oxygen reduction, and the dehydrogenation of ammonia borane, formic acid, hydrous hydrazine, and hydrazine borane. The use of synergistic catalysis in a number of other reactions is also discussed.</P><p>[Review]<br />Ashish Kumar Singh, Qiang Xu<br /><i>ChemCatChem</i> <b>2013</b>, <i>5</i>, No. 3, 652. <a href="http://dx.doi.org/10.1002/cctc.201200591">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cctc.201200699">
<title>Enhancing Oxidative Dehydrogenation Selectivity of Ceria-Based Catalysts with Phosphorus as Additive</title>
<link>http://dx.doi.org/10.1002/cctc.201200699</link>
<dc:creator>Ioan-Teodor Trotu&#x15F;, Cristian M. Teodorescu, Vasile I. P&#xE2;rvulescu, Ioan-Cezar Marcu</dc:creator>
<dc:date>2013-01-22T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/cctc.201200699.gif" alt="Enhancing Oxidative Dehydrogenation Selectivity of Ceria-Based Catalysts with Phosphorus as Additive" style="float:left; padding-right: 10px" /></p><P><B>Rise to the top:</B> A series of phosphated ceria catalysts were studied and presented an increase in oxidative dehydrogenation selectivity with respect to pure ceria, mainly at the expense of total oxidation selectivity. Thus, the selectivity to propene was approximately 74 % with surface-phosphated catalysts and 62 % with bulk-phosphated catalysts.</P><p>[Full Paper]<br />Ioan-Teodor Trotu&#x015F;, Cristian M. Teodorescu, Vasile I. P&acirc;rvulescu, Ioan-Cezar Marcu<br /><i>ChemCatChem</i> <b>2013</b>, <i>5</i>, No. 3, 757. <a href="http://dx.doi.org/10.1002/cctc.201200699">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cctc.201200730">
<title>Cyclopalladated Arylimine Self-Assembly Films for Suzuki Reaction</title>
<link>http://dx.doi.org/10.1002/cctc.201200730</link>
<dc:creator>Na Zhao, Tiesheng Li, Zhen Zhai, Jingjing Qiu, Wenjian Xu, Hui Liu, Yangjie Wu</dc:creator>
<dc:date>2013-02-11T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/cctc.201200730.gif" alt="Cyclopalladated Arylimine Self-Assembly Films for Suzuki Reaction" style="float:left; padding-right: 10px" /></p><P><B>Cyclos and cycles:</B> Cyclopalladated arylimine complexes are immobilized on solid slides and characterized. The heterogeneous catalyst obtained exhibits 10 times the catalytic performance of its homogeneous counterpart. None of the reactions require the use of ligands, air isolation, or assistant solvents. The catalysts are run for 8 cycles without deactivation. A Suzuki reaction mechanism is proposed.</P><p>[Full Paper]<br />Na Zhao, Tiesheng Li, Zhen Zhai, Jingjing Qiu, Wenjian Xu, Hui Liu, Yangjie Wu<br /><i>ChemCatChem</i>, February 11, 2013, DOI: 10.1002/cctc.201200730. <a href="http://dx.doi.org/10.1002/cctc.201200730">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/chem.201204186">
<title>Synthesis and Structure of Carbene-Stabilized N-Centered Cations [L&#x3C;sub&#x3E;2&#x3C;/sub&#x3E;N]&#x3C;SUP&#x3E;+&#x3C;/SUP&#x3E;, [L&#x3C;sub&#x3E;2&#x3C;/sub&#x3E;NR]&#x3C;SUP&#x3E;2+&#x3C;/SUP&#x3E;, [LNR&#x3C;sub&#x3E;3&#x3C;/sub&#x3E;]&#x3C;SUP&#x3E;2+&#x3C;/SUP&#x3E;, and [L&#x3C;sub&#x3E;3&#x3C;/sub&#x3E;N]&#x3C;SUP&#x3E;3+&#x3C;/SUP&#x3E;</title>
<link>http://dx.doi.org/10.1002/chem.201204186</link>
<dc:creator>Agnes Kozma, Gopinadhanpillai Gopakumar, Christophe Far&#xE8;s, Walter Thiel, Manuel Alcarazo</dc:creator>
<dc:date>2013-02-21T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/chem.201204186.gif" alt="Synthesis and Structure of Carbene-Stabilized N-Centered Cations [L2N]+, [L2NR]2+, [LNR3]2+, and [L3N]3+" style="float:left; padding-right: 10px" /></p><P><B>Crystallized!</B> Mono-, di-, and tricationic amines that display unprecedented chemical environments around the central nitrogen atom have been structurally characterized. Cyclic voltammetry experiments and density functional calculations have been performed to gain insight into the electronic structure of these new compounds.</P><p>[Communication]<br />Agnes Kozma, Gopinadhanpillai Gopakumar, Christophe Far&egrave;s, Walter Thiel, Manuel Alcarazo<br /><i>Chem. Eur. J.</i> <b>2013</b>, <i>19</i>, No. 11, 3542. <a href="http://dx.doi.org/10.1002/chem.201204186">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/chem.201204385">
<title>Coupling Photocatalysis and Redox Biocatalysis Toward Biocatalyzed Artificial Photosynthesis</title>
<link>http://dx.doi.org/10.1002/chem.201204385</link>
<dc:creator>Sahng Ha Lee, Jae Hong Kim, Chan Beum Park</dc:creator>
<dc:date>2013-02-21T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/chem.201204385.gif" alt="Coupling Photocatalysis and Redox Biocatalysis Toward Biocatalyzed Artificial Photosynthesis" style="float:left; padding-right: 10px" /></p><P><B>Nature versus man-made</B>: Biocatalyzed artificial photosynthesis occurs through the coupling of redox biocatalysis and photocatalysis to mimic natural photosynthesis based on visible-light-driven regeneration of enzyme cofactors. Key design principles for reaction components, such as electron donors, photosensitizers, and electron mediators, are described for artificial photosynthesis involving biocatalytic assemblies.</P><p>[Concept]<br />Sahng Ha Lee, Jae Hong Kim, Chan Beum Park<br /><i>Chem. Eur. J.</i> <b>2013</b>, <i>19</i>, No. 14, 4392. <a href="http://dx.doi.org/10.1002/chem.201204385">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/chem.201300158">
<title>Direct Water Splitting into Hydrogen and Oxygen under Visible Light by using Modified TaON Photocatalysts with d&#x3C;SUP&#x3E;0&#x3C;/SUP&#x3E; Electronic Configuration</title>
<link>http://dx.doi.org/10.1002/chem.201300158</link>
<dc:creator>Kazuhiko Maeda, Daling Lu, Kazunari Domen</dc:creator>
<dc:date>2013-03-28T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/chem.201300158.gif" alt="Direct Water Splitting into Hydrogen and Oxygen under Visible Light by using Modified TaON Photocatalysts with d0 Electronic Configuration" style="float:left; padding-right: 10px" /></p><P><B>Parting water!</B> Direct splitting of pure water into H<sub>2</sub> and O<sub>2</sub> under visible light (<I>&lambda;</I>&gt;400 nm) was achieved by using a modified TaON photocatalyst with d<SUP>0</SUP> electronic configuration. Modification of a less-defective TaON (ZrO<sub>2</sub>/TaON) with core/shell-structured RuO<sub><I>x</I></sub>/Cr<sub>2</sub>O<sub>3</sub> nanoparticles and colloidal IrO<sub>2</sub> was found to be indispensable to achieving the reaction (see figure).</P><p>[Communication]<br />Kazuhiko Maeda, Daling Lu, Kazunari Domen<br /><i>Chem. Eur. J.</i> <b>2013</b>, <i>19</i>, No. 16, 4986. <a href="http://dx.doi.org/10.1002/chem.201300158">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/chem.201300361">
<title>Anion-Driven Reversible Switching of Metal-Centered Stereoisomers in Metallopeptides</title>
<link>http://dx.doi.org/10.1002/chem.201300361</link>
<dc:creator>Naoki Ousaka, Yuki Takeyama, Eiji Yashima</dc:creator>
<dc:date>2013-03-11T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/chem.201300361.gif" alt="Anion-Driven Reversible Switching of Metal-Centered Stereoisomers in Metallopeptides" style="float:left; padding-right: 10px" /></p><P><B>Anion-triggered chiral switch</B>: Reversible switching between <I>fac</I> and <I>mer</I> isomers in tris(2,2'-bipyridine)iron(II) complexes, the ligands of which are substituted at the 5-position with various peptides of different lengths and sequences, has been achieved (see figure). The remote stereocontrol at the Fe<SUP>II</SUP> center by a domino-type chiral information transfer along an achiral peptide main-chain was observed even over 3 nm (50 bond lengths).</P><p>[Communication]<br />Naoki Ousaka, Yuki Takeyama, Eiji Yashima<br /><i>Chem. Eur. J.</i> <b>2013</b>, <i>19</i>, No. 15, 4680. <a href="http://dx.doi.org/10.1002/chem.201300361">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cmdc.201200516">
<title>Optimization of Marine Triterpene Sipholenols as Inhibitors of Breast Cancer Migration and Invasion</title>
<link>http://dx.doi.org/10.1002/cmdc.201200516</link>
<dc:creator>Ahmed I. Foudah, Sandeep Jain, Belnaser A. Busnena, Khalid A. El Sayed</dc:creator>
<dc:date>2013-02-12T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/cmdc.201200516.gif" alt="Optimization of Marine Triterpene Sipholenols as Inhibitors of Breast Cancer Migration and Invasion" style="float:left; padding-right: 10px" /></p><P><B>Sipholenol A</B>, a sipholane triterpene from <I>Callyspongia siphonella</I>, and its analogues are shown to have antimigratory activity in metastatic human breast cancer cells, while exhibiting no cytotoxicity towards normal epithelial cells. Evaluation of 19,20-anhydrosipholenol A 4&beta;-benzoate ester against 451 human protein kinases identified protein tyrosine kinase 6 as a potential target. Sipholane triterpenoids represent novel antimigratory marine natural products with potential for development against metastatic malignancies.</P><p>[Full Paper]<br />Ahmed I. Foudah, Sandeep Jain, Belnaser A. Busnena, Khalid A. El Sayed<br /><i>ChemMedChem</i> <b>2013</b>, <i>8</i>, No. 3, 497. <a href="http://dx.doi.org/10.1002/cmdc.201200516">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cmdc.201200562">
<title>Synthesis and Biological Evaluation of Purine 2&#x27;-Fluoro-2&#x27;-deoxyriboside ProTides as Anti-influenza Virus Agents</title>
<link>http://dx.doi.org/10.1002/cmdc.201200562</link>
<dc:creator>Silvia Meneghesso, Evelien Vanderlinden, Andrea Brancale, Jan Balzarini, Lieve Naesens, Christopher McGuigan</dc:creator>
<dc:date>2013-02-05T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/cmdc.201200562.gif" alt="Synthesis and Biological Evaluation of Purine 2'-Fluoro-2'-deoxyriboside ProTides as Anti-influenza Virus Agents" style="float:left; padding-right: 10px" /></p><P><B>Tidal power:</B> We report the synthesis and biological evaluation of several ProTides of 6-modified analogues of 2'-fluoro-2'-deoxyguanosine as anti-influenza agents. The superiority of the ProTides over the parent nucleosides was demonstrated in both influenza virus replication assays in MDCK cells and vRNP reconstitution assays in HEK-293T cells.</P><p>[Full Paper]<br />Silvia Meneghesso, Evelien Vanderlinden, Andrea Brancale, Jan Balzarini, Lieve Naesens, Christopher McGuigan<br /><i>ChemMedChem</i> <b>2013</b>, <i>8</i>, No. 3, 415. <a href="http://dx.doi.org/10.1002/cmdc.201200562">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cmdc.201200580">
<title>Monitoring Binding of HIV-1 Capsid Assembly Inhibitors Using &#x3C;SUP&#x3E;19&#x3C;/SUP&#x3E;F Ligand-and &#x3C;SUP&#x3E;15&#x3C;/SUP&#x3E;N Protein-Based NMR and X-ray Crystallography: Early Hit Validation of a Benzodiazepine Series</title>
<link>http://dx.doi.org/10.1002/cmdc.201200580</link>
<dc:creator>Nathalie Goudreau, Ren&#xE9; Coulombe, Anne-Marie Faucher, Chantal Grand-Ma&#xEE;tre, Jean-Eric Lacoste, Christopher T. Lemke, Eric Malenfant, Yves Bousquet, Lee Fader, Bruno Simoneau, Jean-Fran&#xE7;ois Mercier, Steve Titolo, Stephen W. Mason</dc:creator>
<dc:date>2013-02-10T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/cmdc.201200580.gif" alt="Monitoring Binding of HIV-1 Capsid Assembly Inhibitors Using 19F Ligand-and 15N Protein-Based NMR and X-ray Crystallography: Early Hit Validation of a Benzodiazepine Series" style="float:left; padding-right: 10px" /></p><P><B>CA all the way!</B> Early hits from a series of benzodiazepine inhibitors of viral capsid protein (CA), a novel target against HIV, were characterized using NMR and X-ray co-crystallography. Ligand-based <SUP>19</SUP>F NMR was used to confirm binding specificity and reversibility, and to identify the N-terminal domain (CA<sub>NTD</sub>) as the molecular target. Protein-based NMR identified key residues involved in binding, while X-ray co-crystallography confirmed the binding site and mode. Conformationally restricted cyclic inhibitors further validated the possible binding modes.</P><p>[Full Paper]<br />Nathalie Goudreau, Ren&eacute; Coulombe, Anne-Marie Faucher, Chantal Grand-Ma&icirc;tre, Jean-Eric Lacoste, Christopher T. Lemke, Eric Malenfant, Yves Bousquet, Lee Fader, Bruno Simoneau, Jean-Fran&ccedil;ois Mercier, Steve Titolo, Stephen W. Mason<br /><i>ChemMedChem</i> <b>2013</b>, <i>8</i>, No. 3, 405. <a href="http://dx.doi.org/10.1002/cmdc.201200580">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cmdc.201200584">
<title>Computational Studies Identifying Entry Inhibitor Scaffolds Targeting the Phe 43 Cavity of HIV-1 gp120</title>
<link>http://dx.doi.org/10.1002/cmdc.201200584</link>
<dc:creator>Cristina Tintori, Manikandan Selvaraj, Roger Badia, Bonaventura Clotet, Jos&#xE9; A. Est&#xE9;, Maurizio Botta</dc:creator>
<dc:date>2013-02-12T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/cmdc.201200584.gif" alt="Computational Studies Identifying Entry Inhibitor Scaffolds Targeting the Phe 43 Cavity of HIV-1 gp120" style="float:left; padding-right: 10px" /></p><P><B>Antiviral identification:</B> Using a virtual screening protocol, &sim;250 000 commercially available compounds were theoretically evaluated for potential anti-HIV activity through disruption of the gp120&ndash;CD4 interface. Twenty hits were subsequently evaluated in vitro, identifying four novel chemical scaffolds with EC<sub>50</sub> values ranging between 25&ndash;0.9 &mu;<span style="font-variant:small-caps">M</span> against wild-type (NL4-3) HIV-1-infected MT-4 cells. Phe 43 cavity of gp120 was confirmed as the target by a mutation experiment, being the Met 475 Ile mutant strain resistant to these agents.</P><p>[Full Paper]<br />Cristina Tintori, Manikandan Selvaraj, Roger Badia, Bonaventura Clotet, Jos&eacute; A. Est&eacute;, Maurizio Botta<br /><i>ChemMedChem</i> <b>2013</b>, <i>8</i>, No. 3, 475. <a href="http://dx.doi.org/10.1002/cmdc.201200584">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201200840">
<title>Interactions of Aromatic Radicals with Water</title>
<link>http://dx.doi.org/10.1002/cphc.201200840</link>
<dc:creator>Rachel Crespo-Otero, Kenny Bravo-Rodriguez, Saonli Roy, Tobias Benighaus, Walter Thiel, Wolfram Sander, Elsa S&#xE1;nchez-Garc&#xED;a</dc:creator>
<dc:date>2013-01-18T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/cphc.201200840.gif" alt="Interactions of Aromatic Radicals with Water" style="float:left; padding-right: 10px" /></p><P><B>Complex radical interactions:</B> The complexes of aromatic radicals and water are investigated using computational methods (see picture) and (for the benzyl radical&ndash;water complex) by matrix isolation experiments.</P><p>[Article]<br />Rachel Crespo-Otero, Kenny Bravo-Rodriguez, Saonli Roy, Tobias Benighaus, Walter Thiel, Wolfram Sander, Elsa S&aacute;nchez-Garc&iacute;a<br /><i>ChemPhysChem</i> <b>2013</b>, <i>14</i>, No. 4, 805. <a href="http://dx.doi.org/10.1002/cphc.201200840">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201201075">
<title>Visible-Light-Active Elemental Photocatalysts</title>
<link>http://dx.doi.org/10.1002/cphc.201201075</link>
<dc:creator>Gang Liu, Ping Niu, Hui-Ming Cheng</dc:creator>
<dc:date>2013-02-18T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/cphc.201201075.gif" alt="Visible-Light-Active Elemental Photocatalysts" style="float:left; padding-right: 10px" /></p><P><B>Elemental photocatalysts</B> are emerging as a new class of visible-light-responsive catalytic materials for applications in pollutant degradation and water splitting.</P><p>[Concept]<br />Gang Liu, Ping Niu, Hui-Ming Cheng<br /><i>ChemPhysChem</i> <b>2013</b>, <i>14</i>, No. 5, 885. <a href="http://dx.doi.org/10.1002/cphc.201201075">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201201083">
<title>&#x3C;B&#x3E;Molecular Switching Behavior in Isosteric DNA Base Pairs&#x3C;/B&#x3E;</title>
<link>http://dx.doi.org/10.1002/cphc.201201083</link>
<dc:creator>A. K. Jissy, Sukanya Konar, Ayan Datta</dc:creator>
<dc:date>2013-02-20T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/cphc.201201083.gif" alt="Molecular Switching Behavior in Isosteric DNA Base Pairs" style="float:left; padding-right: 10px" /></p><P><B>Paired up:</B> The structures and proton-coupled behavior of adenine&ndash;thymine and a modified base pair containing a thymine isostere, adenine&ndash;difluorotoluene (A-F), are studied in different solvents by dispersion-corrected density functional theory. DNA sequences capable of changing their sequence conformation on protonation are used in the construction of pH-based molecular switches (see picture).</P><p>[Article]<br />A. K. Jissy, Sukanya Konar, Ayan Datta<br /><i>ChemPhysChem</i> <b>2013</b>, <i>14</i>, No. 6, 1219. <a href="http://dx.doi.org/10.1002/cphc.201201083">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cphc.201300027">
<title>Design of a Highly Efficient O&#x3C;sub&#x3E;2&#x3C;/sub&#x3E; Cathode Based on Bilirubin Oxidase from &#x3C;I&#x3E;Magnaporthe oryzae&#x3C;/I&#x3E;</title>
<link>http://dx.doi.org/10.1002/cphc.201300027</link>
<dc:creator>Marine Cadet, Xavier Brilland, S&#xE9;bastien Gounel, Fr&#xE9;d&#xE9;ric Louerat, Nicolas Mano</dc:creator>
<dc:date>2013-02-07T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/cphc.201300027.gif" alt="Design of a Highly Efficient O2 Cathode Based on Bilirubin Oxidase from Magnaporthe oryzae" style="float:left; padding-right: 10px" /></p><P><B>Fungi for the better:</B> The so far highest known current density (1.37 mA cm<SUP>&minus;2</SUP>) for the enzymatic O<sub>2</sub> reduction under physiological conditions is reported. This is achieved by the design of a new redox polymer with an increased catalytic site density and by using a new bilirubin oxidase (BOD) from <I>Magnaporthe oryzae</I>.</P><p>[Communication]<br />Marine Cadet, Xavier Brilland, S&eacute;bastien Gounel, Fr&eacute;d&eacute;ric Louerat, Nicolas Mano<br /><i>ChemPhysChem</i>, February 7, 2013, DOI: 10.1002/cphc.201300027. <a href="http://dx.doi.org/10.1002/cphc.201300027">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cplu.201200206">
<title>Microwave-Assisted In Situ Synthesis of Graphene/PEDOT Hybrid and Its Application in Supercapacitors
</title>
<link>http://dx.doi.org/10.1002/cplu.201200206</link>
<dc:creator>Dong Sun, Li Jin, Yun Chen, Jian-Rong Zhang, Jun-Jie Zhu</dc:creator>
<dc:date>2012-12-28T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/cplu.201200206.gif" alt="Microwave-Assisted In Situ Synthesis of Graphene/PEDOT Hybrid and Its Application in Supercapacitors
" style="float:left; padding-right: 10px" /></p><P><B>Do it in the microwave</B>: A graphene/poly(3,4-ethylenedioxythiophene) (G/PEDOT) hybrid has been prepared by the in situ polymerization of EDOT monomer using the precursor of graphene, graphene oxide, as an oxidant under microwave heating. The G/PEDOT hybrid as a supercapacitor material exhibits high specific capacitance (see figure), excellent electrochemical stability, and high energy density.</P><p>[Full Paper]<br />Dong Sun, Li Jin, Yun Chen, Jian-Rong Zhang, Jun-Jie Zhu<br /><i>ChemPlusChem</i> <b>2013</b>, <i>78</i>, No. 3, 227. <a href="http://dx.doi.org/10.1002/cplu.201200206">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cplu.201200287">
<title>Controllable Fabrication of CuS Hierarchical Nanostructures and Their Optical, Photocatalytic, and Wave Absorption Properties</title>
<link>http://dx.doi.org/10.1002/cplu.201200287</link>
<dc:creator>Shuai He, Guang-Sheng Wang, Chang Lu, Xin Luo, Bo Wen, Lin Guo, Mao-Sheng Cao</dc:creator>
<dc:date>2013-01-10T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/cplu.201200287.gif" alt="Controllable Fabrication of CuS Hierarchical Nanostructures and Their Optical, Photocatalytic, and Wave Absorption Properties" style="float:left; padding-right: 10px" /></p><P><B>A series of CuS hierarchical</B> nanostructures have been synthesized. The CuS nanostructures with large surface area show excellent photocatalytic degradation of methylene blue. The formation mechanism of the hierarchical structures was discussed. Selected CuS nanostructures possess excellent microwave absorbing properties. When the absorbers have a thickness is 3.5 mm, the minimum reflection loss can reach &minus;76.4 dB at 12.64 GHz (see graph).</P><p>[Full Paper]<br />Shuai He, Guang-Sheng Wang, Chang Lu, Xin Luo, Bo Wen, Lin Guo, Mao-Sheng Cao<br /><i>ChemPlusChem</i> <b>2013</b>, <i>78</i>, No. 3, 250. <a href="http://dx.doi.org/10.1002/cplu.201200287">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cplu.201200289">
<title>Direct Growth of Fe&#x3C;sub&#x3E;2&#x3C;/sub&#x3E;V&#x3C;sub&#x3E;4&#x3C;/sub&#x3E;O&#x3C;sub&#x3E;13&#x3C;/sub&#x3E; Nanoribbons on a Stainless-Steel Mesh for Visible-Light Photoreduction of CO&#x3C;sub&#x3E;2&#x3C;/sub&#x3E; into Renewable Hydrocarbon Fuel and Degradation of Gaseous Isopropyl Alcohol</title>
<link>http://dx.doi.org/10.1002/cplu.201200289</link>
<dc:creator>Ping Li, Yong Zhou, Wenguang Tu, Qi Liu, Shicheng Yan, Zhigang Zou</dc:creator>
<dc:date>2013-01-18T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/cplu.201200289.gif" alt="Direct Growth of Fe2V4O13 Nanoribbons on a Stainless-Steel Mesh for Visible-Light Photoreduction of CO2 into Renewable Hydrocarbon Fuel and Degradation of Gaseous Isopropyl Alcohol" style="float:left; padding-right: 10px" /></p><P><B>Recyclable ribbons</B>: Fe<sub>2</sub>V<sub>4</sub>O<sub>13</sub> nanoribbons (see figure) growing on a stainless-steel mesh were fabricated by a simple and facile hydrothermal reaction. The nanoribbons can be easily recycled and used in the photocatalytic conversion of CO<sub>2</sub> into renewable hydrocarbon fuel (CH<sub>4</sub>) and in the degradation of gaseous isopropyl alcohol.</P><p>[Full Paper]<br />Ping Li, Yong Zhou, Wenguang Tu, Qi Liu, Shicheng Yan, Zhigang Zou<br /><i>ChemPlusChem</i> <b>2013</b>, <i>78</i>, No. 3, 274. <a href="http://dx.doi.org/10.1002/cplu.201200289">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cplu.201200296">
<title>Folic Acid Functionalized Nanoprobes for Fluorescence-, Dark-Field-, and Dual-Imaging-Based Selective Detection of Cancer Cells and Tissue</title>
<link>http://dx.doi.org/10.1002/cplu.201200296</link>
<dc:creator>Amit Ranjan Maity, Arindam Saha, Arun Roy, Nikhil R. Jana</dc:creator>
<dc:date>2013-01-17T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/cplu.201200296.gif" alt="Folic Acid Functionalized Nanoprobes for Fluorescence-, Dark-Field-, and Dual-Imaging-Based Selective Detection of Cancer Cells and Tissue" style="float:left; padding-right: 10px" /></p><P><B>Probes with a preference</B>: Folate-functionalized quantum dots, gold/silver nanoparticles, and magnetic quantum dots have been synthesized and used as fluorescence, dark-field, and dual-imaging probes for the selective detection of cancer cells and tissues (see figure).</P><p>[Full Paper]<br />Amit Ranjan Maity, Arindam Saha, Arun Roy, Nikhil R. Jana<br /><i>ChemPlusChem</i> <b>2013</b>, <i>78</i>, No. 3, 259. <a href="http://dx.doi.org/10.1002/cplu.201200296">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cssc.201200671">
<title>Limitations for Current Production in &#x3C;I&#x3E;Geobacter sulfurreducens&#x3C;/I&#x3E; Biofilms</title>
<link>http://dx.doi.org/10.1002/cssc.201200671</link>
<dc:creator>P. Sebastian Bonanni, Dan F. Bradley, Germ&#xE1;n D. Schrott, Juan Pablo Busalmen</dc:creator>
<dc:date>2013-02-18T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/cssc.201200671.gif" alt="Limitations for Current Production in Geobacter sulfurreducens Biofilms" style="float:left; padding-right: 10px" /></p><P><B>Hop, skip, and jump:</B> A mathematical model that allows the identification of limiting steps for current production under several experimental conditions and in different layers of a biofilm is presented. A comparison of model outputs considering electron hopping and conduction through pili indicates that only electron hopping can account for some recent experimental results.</P><p>[Full Paper]<br />P. Sebastian Bonanni, Dan F. Bradley, Germ&aacute;n D. Schrott, Juan Pablo Busalmen<br /><i>ChemSusChem</i> <b>2013</b>, <i>6</i>, No. 4, 711. <a href="http://dx.doi.org/10.1002/cssc.201200671">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cssc.201200692">
<title>Emulsion-Templated Macroporous Carbons Synthesized By Hydrothermal Carbonization and their Application for the Enzymatic Oxidation of Glucose</title>
<link>http://dx.doi.org/10.1002/cssc.201200692</link>
<dc:creator>Nicolas Brun, Lise Edembe, S&#xE9;bastien Gounel, Nicolas Mano, Magdalena M. Titirici</dc:creator>
<dc:date>2013-03-11T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/cssc.201200692.gif" alt="Emulsion-Templated Macroporous Carbons Synthesized By Hydrothermal Carbonization and their Application for the Enzymatic Oxidation of Glucose" style="float:left; padding-right: 10px" /></p><P><B>Baking biomass!</B> Highly porous carbonaceous monoliths are designed and synthesized from a sustainable saccharide derivative. With furfural as the carbon precursor and using a carbonization method that is based on using a concentrated direct emulsion as a soft-template, a graphitized carbon framework was produced. As a proof of principle, these new carbons are successfully used as electrodes for enzymatic biofuel cells.</P><p>[Full Paper]<br />Nicolas Brun, Lise Edembe, S&eacute;bastien Gounel, Nicolas Mano, Magdalena M. Titirici<br /><i>ChemSusChem</i> <b>2013</b>, <i>6</i>, No. 4, 701. <a href="http://dx.doi.org/10.1002/cssc.201200692">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cssc.201200778">
<title>Pd-modified Au on Carbon as an Effective and Durable Catalyst for the Direct Oxidation of HMF to 2,5-Furandicarboxylic Acid</title>
<link>http://dx.doi.org/10.1002/cssc.201200778</link>
<dc:creator>Alberto Villa, Marco Schiavoni, Sebastiano Campisi, Gabriel M. Veith, Laura Prati</dc:creator>
<dc:date>2013-03-11T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/cssc.201200778.gif" alt="Pd-modified Au on Carbon as an Effective and Durable Catalyst for the Direct Oxidation of HMF to 2,5-Furandicarboxylic Acid" style="float:left; padding-right: 10px" /></p><P><B>Mixed noblility:</B> We show that the modification of a gold/carbon catalyst with platinum or palladium produces stable and recyclable catalysts for the selective oxidation of 5-hydroxymethylfurfural (HMF) to 2,5-furandicarboxylic acid (FDCA): the support and nanoparticle chemistry directly mediate the selective oxidation of terminal hydroxyl groups in bio-derived HMF. This finding is a significant advance over current conversion technology because of the technological importance of FDCA.</P><p>[Communication]<br />Alberto Villa, Marco Schiavoni, Sebastiano Campisi, Gabriel M. Veith, Laura Prati<br /><i>ChemSusChem</i> <b>2013</b>, <i>6</i>, No. 4, 609. <a href="http://dx.doi.org/10.1002/cssc.201200778">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/cssc.201200880">
<title>Cellulose Conversion with Tungstated-Alumina-Based Catalysts: Influence of the Presence of Platinum and Mechanistic Studies</title>
<link>http://dx.doi.org/10.1002/cssc.201200880</link>
<dc:creator>Flora Chambon, Franck Rataboul, Catherine Pinel, Amandine Cabiac, Emmanuelle Guillon, Nadine Essayem</dc:creator>
<dc:date>2013-02-20T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/cssc.201200880.gif" alt="Cellulose Conversion with Tungstated-Alumina-Based Catalysts: Influence of the Presence of Platinum and Mechanistic Studies" style="float:left; padding-right: 10px" /></p><P><B>Support for platinum:</B> The hydrothermal treatment of cellulose under H<sub>2</sub> in the presence of tungstated alumina-based catalysts (AlW) yields lactic acid or acetol and propylene glycol as the main products depending on the presence or absence of supported platinum.</P><p>[Full Paper]<br />Flora Chambon, Franck Rataboul, Catherine Pinel, Amandine Cabiac, Emmanuelle Guillon, Nadine Essayem<br /><i>ChemSusChem</i> <b>2013</b>, <i>6</i>, No. 3, 500. <a href="http://dx.doi.org/10.1002/cssc.201200880">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201201346">
<title>X-ray Crystallographic and First-Principles Theoretical Studies of K&#x3C;sub&#x3E;2&#x3C;/sub&#x3E;[TcOCl&#x3C;sub&#x3E;5&#x3C;/sub&#x3E;] and UV/Vis Investigation of the [TcOCl&#x3C;sub&#x3E;5&#x3C;/sub&#x3E;]&#x3C;SUP&#x3E;2&#x2013;&#x3C;/SUP&#x3E; and [TcOCl&#x3C;sub&#x3E;4&#x3C;/sub&#x3E;]&#x3C;SUP&#x3E;&#x2013;&#x3C;/SUP&#x3E; Ions</title>
<link>http://dx.doi.org/10.1002/ejic.201201346</link>
<dc:creator>Erik V. Johnstone, Philippe F. Weck, Frederic Poineau, Eunja Kim, Paul M. Forster, Alfred P. Sattelberger, Kenneth R. Czerwinski</dc:creator>
<dc:date>2013-01-23T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/ejic.201201346.jpg" alt="X-ray Crystallographic and First-Principles Theoretical Studies of K2[TcOCl5] and UV/Vis Investigation of the [TcOCl5]2&ndash; and [TcOCl4]&ndash; Ions" style="float:left; padding-right: 10px" /></p><P>Dipotassium pentachloridooxidotechnetate has been isolated as single crystals and its structure investigated by crystallographic and first-principles theoretical techniques.</P><p>[Short Communication]<br />Erik V. Johnstone, Philippe F. Weck, Frederic Poineau, Eunja Kim, Paul M. Forster, Alfred P. Sattelberger, Kenneth R. Czerwinski<br /><i>Eur. J. Inorg. Chem.</i> <b>2013</b>, No. 7, 1097. <a href="http://dx.doi.org/10.1002/ejic.201201346">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201201427">
<title>An Experimental and Theoretical Approach to the Photophysical Properties of Some Rh and Ir Complexes Incorporating the Dipyrromethene Ligand</title>
<link>http://dx.doi.org/10.1002/ejic.201201427</link>
<dc:creator>Diane Ramlot, Mateusz Rebarz, Leen Volker, Margriet Ovaere, David Beljonne, Wim Dehaen, Luc Van Meervelt, C&#xE9;cile Moucheron, Andr&#xE9;e Kirsch-De Mesmaeker</dc:creator>
<dc:date>2013-02-13T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/ejic.201201427.jpg" alt="An Experimental and Theoretical Approach to the Photophysical Properties of Some Rh and Ir Complexes Incorporating the Dipyrromethene Ligand" style="float:left; padding-right: 10px" /></p><P>The spectroscopic properties of Rh and Ir complexes that contain <I>meso</I>-<I>p</I>-methoxyphenyldipyrromethene (dipyH) and phenylpyridine (ppy) ligands, [Rh(dipy)<sub>3</sub>], [Rh(ppy)<sub>2</sub>(dipy)] and [Ir(ppy)<sub>2</sub>(dipy)], are described and discussed from experimental and theoretical approaches.</P><p>[Full Paper]<br />Diane Ramlot, Mateusz Rebarz, Leen Volker, Margriet Ovaere, David Beljonne, Wim Dehaen, Luc Van Meervelt, C&eacute;cile Moucheron, Andr&eacute;e Kirsch-De Mesmaeker<br /><i>Eur. J. Inorg. Chem.</i> <b>2013</b>, No. 12, 2031. <a href="http://dx.doi.org/10.1002/ejic.201201427">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201201485">
<title>Enantioselective Ir-Catalyzed Hydrogenation of Minimally Functionalized Olefins Using Pyranoside Phosphinite-Oxazoline Ligands</title>
<link>http://dx.doi.org/10.1002/ejic.201201485</link>
<dc:creator>Javier Mazuela, Oscar P&#xE0;mies, Montserrat Di&#xE9;guez</dc:creator>
<dc:date>2013-02-21T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/ejic.201201485.jpg" alt="Enantioselective Ir-Catalyzed Hydrogenation of Minimally Functionalized Olefins Using Pyranoside Phosphinite-Oxazoline Ligands" style="float:left; padding-right: 10px" /></p><P>Pyranoside phosphinite-oxazoline ligands were successfully applied in the asymmetric Ir-catalyzed hydrogenation of a wide range of minimally functionalized olefins (<I>ee</I> up to 99 %). The introduction of a bulky <I>ortho</I>-tolyl phosphinite moiety was crucial to achieving the highest enantioselectivities with some of the most challenging substrate types.</P><p>[Full Paper]<br />Javier Mazuela, Oscar P&agrave;mies, Montserrat Di&eacute;guez<br /><i>Eur. J. Inorg. Chem.</i> <b>2013</b>, No. 12, 2139. <a href="http://dx.doi.org/10.1002/ejic.201201485">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejic.201201518">
<title>B-Mercaptocarboranes: A New Synthetic Route</title>
<link>http://dx.doi.org/10.1002/ejic.201201518</link>
<dc:creator>Kuanysh Z. Kabytaev, Thomas A. Everett, Alexander V. Safronov, Yulia V. Sevryugina, Satish S. Jalisatgi, M. Frederick Hawthorne</dc:creator>
<dc:date>2013-02-04T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/ejic.201201518.jpg" alt="B-Mercaptocarboranes: A New Synthetic Route" style="float:left; padding-right: 10px" /></p><P>A new synthetic route is described for the Pd-catalyzed preparation of mono- and di-B-mercapto(<I>ortho</I>-, <I>meta</I>-, and <I>para</I>-)carboranes from iodocarboranes and a sulfur nucleophile (TIPS&ndash;SH).</P><p>[Short Communication]<br />Kuanysh Z. Kabytaev, Thomas A. Everett, Alexander V. Safronov, Yulia V. Sevryugina, Satish S. Jalisatgi, M. Frederick Hawthorne<br /><i>Eur. J. Inorg. Chem.</i> <b>2013</b>, No. 14, 2488. <a href="http://dx.doi.org/10.1002/ejic.201201518">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201201580">
<title>Stereoselective Synthesis of &#x3B1;-Glycosyl Azides by TMSOTf-Mediated Ring Opening of 1,6-Anhydro Sugars</title>
<link>http://dx.doi.org/10.1002/ejoc.201201580</link>
<dc:creator>Mathieu L. Lepage, Anne Bodlenner, Philippe Compain</dc:creator>
<dc:date>2013-02-18T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/ejoc.201201580.jpg" alt="Stereoselective Synthesis of &alpha;-Glycosyl Azides by TMSOTf-Mediated Ring Opening of 1,6-Anhydro Sugars" style="float:left; padding-right: 10px" /></p><P>A new route to &alpha;-glycosyl azides by way of TMSN<sub>3</sub> ring-opening of 1,6-anhydro sugars is presented. The potential of this methodology is demonstrated by the expeditious synthesis of a pseudopentasaccharide following a &ldquo;click-click&rdquo; approach.</P><p>[Full Paper]<br />Mathieu L. Lepage, Anne Bodlenner, Philippe Compain<br /><i>Eur. J. Org. Chem.</i> <b>2013</b>, No. 10, 1963. <a href="http://dx.doi.org/10.1002/ejoc.201201580">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201201594">
<title>Asymmetric Synthesis of (1,5)Naphthalenophanes by Dehydro-Diels&#x2013;Alder Reaction</title>
<link>http://dx.doi.org/10.1002/ejoc.201201594</link>
<dc:creator>Pablo Wessig, Annika Matthes, Uwe Schilde, Alexandra Kelling</dc:creator>
<dc:date>2013-02-21T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/ejoc.201201594.jpg" alt="Asymmetric Synthesis of (1,5)Naphthalenophanes by Dehydro-Diels&ndash;Alder Reaction" style="float:left; padding-right: 10px" /></p><P>The asymmetric dehydro-Diels&ndash;Alder (ADDA) reaction to axially chiral (1,5)naphthalenophanes was investigated. Using chiral auxiliaries, both photochemical and thermal DDA provided the target compounds, in which the latter approach provided better results in regard to yields and stereoselectivity. Furthermore, the mechanism of the DDA reaction was investigated by means of DFT calculations.</P><p>[Full Paper]<br />Pablo Wessig, Annika Matthes, Uwe Schilde, Alexandra Kelling<br /><i>Eur. J. Org. Chem.</i> <b>2013</b>, No. 11, 2123. <a href="http://dx.doi.org/10.1002/ejoc.201201594">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201300010">
<title>Direct Hydrosilylation of Tertiary Amides to Amines by an In Situ Formed Iron/N-Heterocyclic Carbene Catalyst</title>
<link>http://dx.doi.org/10.1002/ejoc.201300010</link>
<dc:creator>Alexey Volkov, Elina Buitrago, Hans Adolfsson</dc:creator>
<dc:date>2013-03-01T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/ejoc.201300010.jpg" alt="Direct Hydrosilylation of Tertiary Amides to Amines by an In Situ Formed Iron/N-Heterocyclic Carbene Catalyst" style="float:left; padding-right: 10px" /></p><P>Tertiary amides are reduced to their corresponding tertiary amines in high isolated yields by using the polymeric silane polymethylhydrosiloxane (PMHS) in the presence of an in situ generated iron/N-heterocyclic carbene complex (1 mol-%), generated from iron(II) acetate and 1-(2-hydroxy-2-phenylethyl)-3-methylimidazolium triflate ([PhHEMIM][OTF]), and a catalytic amount of lithium chloride (1 mol-%).</P><p>[Short Communication]<br />Alexey Volkov, Elina Buitrago, Hans Adolfsson<br /><i>Eur. J. Org. Chem.</i> <b>2013</b>, No. 11, 2066. <a href="http://dx.doi.org/10.1002/ejoc.201300010">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/ejoc.201300112">
<title>Stereoselective Synthesis of (&#x3C;I&#x3E;E&#x3C;/I&#x3E;)-&#x3B1;,&#x3B2;-Dehydroamino Acid Esters</title>
<link>http://dx.doi.org/10.1002/ejoc.201300112</link>
<dc:creator>Yoko Yasuno, Makoto Hamada, Takeshi Yamada, Tetsuro Shinada, Yasufumi Ohfune</dc:creator>
<dc:date>2013-02-25T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/ejoc.201300112.jpg" alt="Stereoselective Synthesis of (E)-&alpha;,&beta;-Dehydroamino Acid Esters" style="float:left; padding-right: 10px" /></p><P>A variety of (<I>E</I>)-dehydroamino acid esters were stereoselectively synthesized by using (diphenylphosphono)glycinate. The stereoselectivity was influenced by metal additives. Various (<I>E</I>)-dehydroamino acid esters were prepared by the condensation reaction of the new phosphonates with easily available aldehydes by choosing the appropriate reaction conditions.</P><p>[Short Communication]<br />Yoko Yasuno, Makoto Hamada, Takeshi Yamada, Tetsuro Shinada, Yasufumi Ohfune<br /><i>Eur. J. Org. Chem.</i> <b>2013</b>, No. 10, 1884. <a href="http://dx.doi.org/10.1002/ejoc.201300112">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/open.201200039">
<title>Fluorinated Boron-Dipyrromethene (BODIPY) Dyes: Bright and Versatile Probes for Surface Analysis</title>
<link>http://dx.doi.org/10.1002/open.201200039</link>
<dc:creator>Mandy Hecht, Tobias Fischer, Paul Dietrich, Werner Kraus, Ana B. Descalzo, Wolfgang E. S. Unger, Knut Rurack</dc:creator>
<dc:date>2013-01-09T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/open.201200039.gif" alt="Fluorinated Boron-Dipyrromethene (BODIPY) Dyes: Bright and Versatile Probes for Surface Analysis" style="float:left; padding-right: 10px" /></p><P><B>Give&lsquo;em fluorine!</B> Bright and highly photostable boron-dipyrromethene (BODIPY) dyes were obtained by the introduction of up to three pentafluoro- or 3,5-bis(trifluoromethyl)phenyl moieties to the BODIPY core, which present a first generation of potent dual X-ray photoelectron spectroscopy (XPS)/fluorescence labels for the quantification of surface functional groups.</P><p>[Full Paper]<br />Mandy Hecht, Tobias Fischer, Paul Dietrich, Werner Kraus, Ana B. Descalzo, Wolfgang E. S. Unger, Knut Rurack<br /><i>ChemistryOpen</i> <b>2013</b>, <i>2</i>, No. 1, 25. <a href="http://dx.doi.org/10.1002/open.201200039">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/open.201200041">
<title>Embedded Palladium Activation as a Facile Method for TiO&#x3C;sub&#x3E;2&#x3C;/sub&#x3E;-Nanotube Nanoparticle Decoration: Cu&#x3C;sub&#x3E;2&#x3C;/sub&#x3E;O-Induced Visible-Light Photoactivity</title>
<link>http://dx.doi.org/10.1002/open.201200041</link>
<dc:creator>Anca Mazare, Ning Liu, Kiyoung Lee, Manuela S. Killian, Patrik Schmuki</dc:creator>
<dc:date>2013-01-10T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/open.201200041.gif" alt="Embedded Palladium Activation as a Facile Method for TiO2-Nanotube Nanoparticle Decoration: Cu2O-Induced Visible-Light Photoactivity" style="float:left; padding-right: 10px" /></p><P><B>Highly decorated!</B> A direct and efficient way to decorate TiO<sub>2</sub> nanotubes with copper, Cu<sub>2</sub>O and CuO particles is shown. Active palladium species embedded in the TiO<sub>2</sub> nanotube walls allow specific initiation sites to be triggered for electroless copper deposition. These Cu<sub>2</sub>O-decorated TiO<sub>2</sub> nanotubes could be used for water splitting.</P><p>[Communication]<br />Anca Mazare, Ning Liu, Kiyoung Lee, Manuela S. Killian, Patrik Schmuki<br /><i>ChemistryOpen</i> <b>2013</b>, <i>2</i>, No. 1, 21. <a href="http://dx.doi.org/10.1002/open.201200041">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/open.201200045">
<title>Carbon Dioxide Adsorption in Betulin-Based Micro- and Macroporous Polyurethanes</title>
<link>http://dx.doi.org/10.1002/open.201200045</link>
<dc:creator>Jekaterina Jeromenok, Winfried B&#xF6;hlmann, Christian J&#xE4;ger, Jens Weber</dc:creator>
<dc:date>2013-01-18T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/open.201200045.gif" alt="Carbon Dioxide Adsorption in Betulin-Based Micro- and Macroporous Polyurethanes" style="float:left; padding-right: 10px" /></p><P><B>Separation of CO<sub>2</sub></B>. Microporous polyurethane networks were prepared based on a renewable resource. Betulin, extracted from birch bark, is used as a structure-directing diol monomer in A<sub>3</sub>-B<sub>2</sub> monomers. The resulting microporous networks show very promising CO<sub>2</sub>/N<sub>2</sub> selectivities. The state of adsorbed CO<sub>2</sub> is analyzed by in situ NMR spectroscopy, and pure physisorption is proven. The preparation of monolithic materials is demonstrated as well.</P><p>[Communication]<br />Jekaterina Jeromenok, Winfried B&ouml;hlmann, Christian J&auml;ger, Jens Weber<br /><i>ChemistryOpen</i> <b>2013</b>, <i>2</i>, No. 1, 17. <a href="http://dx.doi.org/10.1002/open.201200045">Read article.</a></p> ]]></content:encoded>
</item>
<item rdf:about="http://dx.doi.org/10.1002/open.201200046">
<title>Fluoride as Ligand: Chemistry of Some New Terminal and Bridged Systems</title>
<link>http://dx.doi.org/10.1002/open.201200046</link>
<dc:creator>Torben Birk</dc:creator>
<dc:date>2013-01-29T00:00+00:00</dc:date>
<content:encoded><![CDATA[ <p><img src="http://www.wiley-vch.de/util/spotlights/open.201200046.gif" alt="Fluoride as Ligand: Chemistry of Some New Terminal and Bridged Systems" style="float:left; padding-right: 10px" /></p><P><B>Fluorine is unique!</B> A synthesis method for polynuclear systems with bridging fluorido ligands has been developed. The method is based on anchoring and protection of the fluorido ligand by initial coordination to a robust metal center (e.g., Cr<SUP>III</SUP>) and subsequent use of the robust fluoride complex for construction of more complicated polynuclear structures.</P><p>[Thesis Treasury]<br />Torben Birk<br /><i>ChemistryOpen</i> <b>2013</b>, <i>2</i>, No. 1, 13. <a href="http://dx.doi.org/10.1002/open.201200046">Read article.</a></p> ]]></content:encoded>
</item>
</rdf:RDF>