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document.write('<p class="rss-title"><a class="rss-title" href="http://xlink.rsc.org/jumptojournal.cfm?journal_code=OB" target="_self">RSC - Org. Biomol. Chem. latest articles</a><br /><span class="rss-item">RSC - Org. Biomol. Chem. latest articles</span></p>');
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document.write('<li class="rss-item"><a class="rss-item" href="http://xlink.rsc.org/?DOI=b924169h&RSS=1" title="Chemical investigations of a fermentation culture from the endophytic fungus Pestalotiopsis sp. yielded three novel caprolactams, pestalactams A-C (1-3). These compounds are the first C-7 alkylated caprolactam natural products to be reported...." target="_self">Pestalactams A-C: novel caprolactams from the endophytic fungus Pestalotiopsis sp.</a><br />');
document.write('<p><img align=\"center\" src=\"http://www.rsc.org/ejga/OB/2010/b924169h-ga.gif\"/> </p>Rohan A. Davis, Anthony R. Carroll, Katherine T. Andrews, Glen M. Boyle, Truc Linh Tran, Peter C. Healy, John A. Kalaitzis, Roger G. Shivas <br/> (Paper from Org. Biomol. Chem.)<br/> Rohan A. Davis, Org. Biomol. Chem., 2010, DOI: 10.1039/b924169h<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry');
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document.write('<li class="rss-item"><a class="rss-item" href="http://xlink.rsc.org/?DOI=b920443a&RSS=1" title="A carbamate linked quenching group coupled with a pro-quinone methide reactive core provides an effective tool for studying enzyme function without problems associated with background fluorescence. However protein labelling observations should be treated ..." target="_self">Fluorescence quenched quinone methide based activity probes - a cautionary tale</a><br />');
document.write('<p><img align=\"center\" src=\"http://www.rsc.org/ejga/OB/2010/b920443a-ga.gif\"/> </p>Jonathan D. Sellars, Marie Landrum, Aileen Congreve, David P. Dixon, Jackie A. Mosely, Andrew Beeby, Robert Edwards, Patrick G. Steel <br/> (Paper from Org. Biomol. Chem.)<br/> Jonathan D. Sellars, Org. Biomol. Chem., 2010, DOI: 10.1039/b920443a<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry');
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document.write('<li class="rss-item"><a class="rss-item" href="http://xlink.rsc.org/?DOI=b917217c&RSS=1" title="A stereospecific addition/elimination of 2-sulfinyl acrylates using various nucleophiles is demonstrated as a general protocol for alkane- and arenesulfenate generation. A variety of sulfoxides are prepared through alkylation chemistry...." target="_self">Nucleophilic attack of 2-sulfinyl acrylates: A mild and general approach to sulfenic acid anions</a><br />');
document.write('<p><img align=\"center\" src=\"http://www.rsc.org/ejga/OB/2010/b917217c-ga.gif\"/> </p>Suneel P. Singh, Jennifer S. O\'Donnell, Adrian L. Schwan <br/> (Paper from Org. Biomol. Chem.)<br/> Suneel P. Singh, Org. Biomol. Chem., 2010, DOI: 10.1039/b917217c<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry');
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document.write('<li class="rss-item"><a class="rss-item" href="http://xlink.rsc.org/?DOI=b924309g&RSS=1" title="The continuous flow syntheses of a family of butane-2,3-diacetal protected building blocks has been achieved using microreactors in concert with solid supported reagents and scavengers...." target="_self">The continuous flow synthesis of butane-2,3-diacetal protected building blocks using microreactors</a><br />');
document.write('<p><img align=\"center\" src=\"http://www.rsc.org/ejga/OB/2010/b924309g-ga.gif\"/> </p>Catherine F. Carter, Ian R. Baxendale, John B. J. Pavey, Steven V. Ley <br/> (Paper from Org. Biomol. Chem.)<br/> Catherine F. Carter, Org. Biomol. Chem., 2010, DOI: 10.1039/b924309g<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry');
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document.write('<li class="rss-item"><a class="rss-item" href="http://xlink.rsc.org/?DOI=b924721a&RSS=1" title="An efficient, stereocontrolled synthesis of 1-deoxy-7,8-di-epi-castanospermine has been developed involving a vinylogous Mukaiyama aldol reaction (VMAR) and an ene-ene ring closing metathesis reaction (RCM) as key steps...." target="_self">Asymmetric total synthesis of 1-deoxy-7,8-di-epi-castanospermine</a><br />');
document.write('<p><img align=\"center\" src=\"http://www.rsc.org/ejga/OB/2010/b924721a-ga.gif\"/> </p>Vincenzo Zambrano, Gloria Rassu, Annamaria Roggio, Luigi Pinna, Franca Zanardi, Claudio Curti, Giovanni Casiraghi, Lucia Battistini <br/> (Paper from Org. Biomol. Chem.)<br/> Vincenzo Zambrano, Org. Biomol. Chem., 2010, DOI: 10.1039/b924721a<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry');
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document.write('<li class="rss-item"><a class="rss-item" href="http://xlink.rsc.org/?DOI=b917409e&RSS=1" title="The synthesis of 1,4-anhydro-[small beta]-d-galactopyranose (1,5-anhydro-[small alpha]-d-galactofuranose), a proposed intermediate in the ring contraction isomerisation catalyzed by UDP-galactopyranose mutase, together with its [2.2.2] bicyclic methylene ..." target="_self">The UDP-Galp mutase catalyzed isomerization: synthesis and evaluation of 1,4-anhydro-[small beta]-d-galactopyranose and its [2.2.2] methylene homologue</a><br />');
document.write('<p><img align=\"center\" src=\"http://www.rsc.org/ejga/OB/2010/b917409e-ga.gif\"/> </p>Ali Sadeghi-Khomami, Tatiana J. Forcada, Claire Wilson, David A. R. Sanders, Neil R. Thomas <br/> (Paper from Org. Biomol. Chem.)<br/> Ali Sadeghi-Khomami, Org. Biomol. Chem., 2010, DOI: 10.1039/b917409e<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry');
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document.write('<li class="rss-item"><a class="rss-item" href="http://xlink.rsc.org/?DOI=b923249b&RSS=1" title="Zn(OTf)2 acts as an excellent catalyst precursor for addition of various amines to carbodiimides under an atmosphere of air, offering a convenient synthesis of guanidines with high functional-group tolerance. A Zn-N amido species acts as the active specie..." target="_self">Zn(OTf)2-catalyzed addition of amines to carbodiimides: efficient synthesis of guanidines and unpredicted formation of Zn-N amido species</a><br />');
document.write('<p><img align=\"center\" src=\"http://www.rsc.org/ejga/OB/2010/b923249b-ga.gif\"/> </p>Dongzhen Li, Jie Guang, Wen-Xiong Zhang, Yang Wang, Zhenfeng Xi <br/> (Paper from Org. Biomol. Chem.)<br/> Dongzhen Li, Org. Biomol. Chem., 2010, DOI: 10.1039/b923249b<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry');
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document.write('<li class="rss-item"><a class="rss-item" href="http://xlink.rsc.org/?DOI=b922843h&RSS=1" title="Supramolecular fibres are formed by a homochiral synthetic dipeptide incorporating two cyclobutyl rings. Current-sensing AFM shows that once doped, films of the material are capable of conducting electricity...." target="_self">Use of unnatural [small beta]-peptides as a self-assembling component in functional organic fibres</a><br />');
document.write('<p><img align=\"center\" src=\"http://www.rsc.org/ejga/OB/2010/b922843h-ga.gif\"/> </p>Elisabeth Torres, Josep Puigmarti-Luis, Angel Perez del Pino, Rosa M. Ortuno, David B. Amabilino <br/> (Paper from Org. Biomol. Chem.)<br/> Elisabeth Torres, Org. Biomol. Chem., 2010, DOI: 10.1039/b922843h<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry');
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document.write('<li class="rss-item"><a class="rss-item" href="http://xlink.rsc.org/?DOI=b924144b&RSS=1" title="Transketolase mutants have been used with a series of linear and cyclic aliphatic aldehydes, and excellent stereoselectivities observed...." target="_self">Non-[small alpha]-hydroxylated aldehydes with evolved transketolase enzymes</a><br />');
document.write('<p><img align=\"center\" src=\"http://www.rsc.org/ejga/OB/2010/b924144b-ga.gif\"/> </p>Armando Cazares, James L. Galman, Lydia G. Crago, Mark E. B. Smith, John Strafford, Leonardo Rios-Solis, Gary J. Lye, Paul A. Dalby, Helen C. Hailes <br/> (Paper from Org. Biomol. Chem.)<br/> Armando Cazares, Org. Biomol. Chem., 2010, DOI: 10.1039/b924144b<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry');
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document.write('<li class="rss-item"><a class="rss-item" href="http://xlink.rsc.org/?DOI=b924986a&RSS=1" title="2,5-Diarylselenophenes can be prepared by reaction of O-methyl Se-hydrogen phenylphosphonodiselenoate with arylacetylenes or by direct reaction of Woollins\' reagent with 1,4-diarylbutane-1,4-diones...." target="_self">Synthesis of novel 2,5-diarylselenophenes from selenation of 1,4-diarylbutane-1,4-diones or methanol/arylacetylenes</a><br />');
document.write('<p><img align=\"center\" src=\"http://www.rsc.org/ejga/OB/2010/b924986a-ga.gif\"/> </p>Guoxiong Hua, John B. Henry, Yang Li, Andrew R. Mount, Alexandra M. Z. Slawin, J. Derek Woollins <br/> (Paper from Org. Biomol. Chem.)<br/> Guoxiong Hua, Org. Biomol. Chem., 2010, DOI: 10.1039/b924986a<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry');
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document.write('<li class="rss-item"><a class="rss-item" href="http://xlink.rsc.org/?DOI=b925483h&RSS=1" title="Biosynthetic studies with 13C-labelled biosynthetic precursors revealed that the infamous, food-related toxin bongkrekic acid is a polyketide with acetate-derived [small beta]-branches and a carboxylate terminus derived from the methyl group of acetate...." target="_self">Biosynthesis of the mitochondrial adenine nucleotide translocase (ATPase) inhibitor bongkrekic acid in Burkholderia gladioli</a><br />');
document.write('<p><img align=\"center\" src=\"http://www.rsc.org/ejga/OB/2010/b925483h-ga.gif\"/> </p>Barbara Rohm, Kirstin Scherlach, Christian Hertweck <br/> (Communication from Org. Biomol. Chem.)<br/> Barbara Rohm, Org. Biomol. Chem., 2010, DOI: 10.1039/b925483h<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry');
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document.write('<li class="rss-item"><a class="rss-item" href="http://xlink.rsc.org/?DOI=b923336a&RSS=1" title="Treatment of the preformed or the in situ generated aryl/alkyl dithiocarbamates triethylammonium salt with methyl acrylate in an aqueous medium gave solely arylisothiocyanate, whereas the in situ generated aryl dithiocarbamic acid yielded exclusively the ..." target="_self">The thiocarbonyl \'S\' is softer than thiolate \'S\': A catalyst-free one-pot synthesis of isothiocyanates in water</a><br />');
document.write('<p><img align=\"center\" src=\"http://www.rsc.org/ejga/OB/2010/b923336a-ga.gif\"/> </p>Latonglila Jamir, Abdur Rezzak Ali, Harisadhan Ghosh, Francis A. S. Chipem, Bhisma K. Patel <br/> (Paper from Org. Biomol. Chem.)<br/> Latonglila Jamir, Org. Biomol. Chem., 2010, DOI: 10.1039/b923336a<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry');
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document.write('<li class="rss-item"><a class="rss-item" href="http://xlink.rsc.org/?DOI=b921934j&RSS=1" title="Non-heme iron(ii) oxidases (NHIOs) promote a raft of interesting oxidation reactions in vivo. Can we replicate the iron binding environment of the NHIO active site to create biomimetic small-molecule systems that promote hydrocarbon oxidation in vitro?..." target="_self">Design and synthesis of a tetradentate \'3-amine-1-carboxylate\' ligand to mimic the metal binding environment at the non-heme iron(ii) oxidase active site</a><br />');
document.write('<p><img align=\"center\" src=\"http://www.rsc.org/ejga/OB/2010/b921934j-ga.gif\"/> </p>Victoria J. Dungan, Yannick Ortin, Helge Mueller-Bunz, Peter J. Rutledge <br/> (Paper from Org. Biomol. Chem.)<br/> Victoria J. Dungan, Org. Biomol. Chem., 2010, DOI: 10.1039/b921934j<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry');
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document.write('<li class="rss-item"><a class="rss-item" href="http://xlink.rsc.org/?DOI=b922928k&RSS=1" title="Novel modified arginine residues suitable for \'click\' chemistry and their use in a PKC inhibitor is described...." target="_self">Preparation of novel alkylated arginine derivatives suitable for click-cycloaddition chemistry and their incorporation into pseudosubstrate- and bisubstrate-based kinase inhibitors</a><br />');
document.write('<p><img align=\"center\" src=\"http://www.rsc.org/ejga/OB/2010/b922928k-ga.gif\"/> </p>Jeroen van Ameijde, Alex J. Poot, Loek T. M. van Wandelen, Angelique E. M. Wammes, Rob Ruijtenbeek, Dirk T. S. Rijkers, Rob M. J. Liskamp <br/> (Paper from Org. Biomol. Chem.)<br/> Jeroen van Ameijde, Org. Biomol. Chem., 2010, DOI: 10.1039/b922928k<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry');
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document.write('<li class="rss-item"><a class="rss-item" href="http://xlink.rsc.org/?DOI=b924712b&RSS=1" title="Cyclobutane pyrimidine dimers produced in DNA upon UVA irradiation arise from a direct photochemical mechanism rather than a photosensitized process...." target="_self">UVA-induced cyclobutane pyrimidine dimers in DNA: a direct photochemical mechanism?</a><br />');
document.write('<p><img align=\"center\" src=\"http://www.rsc.org/ejga/OB/2010/b924712b-ga.gif\"/> </p>Stephane Mouret, Coralie Philippe, Jocelyne Gracia-Chantegrel, Akos Banyasz, Szilvia Karpati, Dimitra Markovitsi, Thierry Douki <br/> (Paper from Org. Biomol. Chem.)<br/> Stephane Mouret, Org. Biomol. Chem., 2010, DOI: 10.1039/b924712b<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry');
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document.write('<li class="rss-item"><a class="rss-item" href="http://xlink.rsc.org/?DOI=b923754b&RSS=1" title="A highly selective ratiometric fluorescent probe for 1,4-dithiothreitol (DTT) was designed and synthesized, which displays a 66 nm red-shift of fluorescence emission and the color changes from colorless to jade-green upon reaction with DTT...." target="_self">A highly selective ratiometric fluorescent probe for 1,4-dithiothreitol (DTT) detection</a><br />');
document.write('<p><img align=\"center\" src=\"http://www.rsc.org/ejga/OB/2010/b923754b-ga.gif\"/> </p>Baocun Zhu, Xiaoling Zhang, Hongying Jia, Yamin Li, Haipeng Liu, Weihong Tan <br/> (Paper from Org. Biomol. Chem.)<br/> Baocun Zhu, Org. Biomol. Chem., 2010, DOI: 10.1039/b923754b<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry');
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document.write('<li class="rss-item"><a class="rss-item" href="http://xlink.rsc.org/?DOI=b925722e&RSS=1" title="This Emerging Area summarises about 40 years of investigations directed towards asymmetric Si-O couplings, including substrate-, reagent- and catalyst-controlled approaches...." target="_self">Asymmetric Si-O coupling of alcohols</a><br />');
document.write('<p><img align=\"center\" src=\"http://www.rsc.org/ejga/OB/2010/b925722e-ga.gif\"/> </p>Andreas Weickgenannt, Marius Mewald, Martin Oestreich <br/> (Emerging Area from Org. Biomol. Chem.)<br/> Andreas Weickgenannt, Org. Biomol. Chem., 2010, DOI: 10.1039/b925722e<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry');
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document.write('<li class="rss-item"><a class="rss-item" href="http://xlink.rsc.org/?DOI=b926217b&RSS=1" title="Aminomethylated Beaucage\'s reagent 1 was found to be more potent than Beaucage\'s reagent in causing DNA cleavage. This study demonstrated the importance of the amino functionality in enhancing DNA-cleaving activities, and such findings may facilitate de..." target="_self">Thiol-dependent DNA cleavage by aminomethylated Beaucage\'s reagent</a><br />');
document.write('<p><img align=\"center\" src=\"http://www.rsc.org/ejga/OB/2010/b926217b-ga.gif\"/> </p>Jiahui Zheng, Xiaoqian Liu, Qing Yuan, Yoon-Joo Shin, Daekyu Sun, Yixin Lu <br/> (Communication from Org. Biomol. Chem.)<br/> Jiahui Zheng, Org. Biomol. Chem., 2010, DOI: 10.1039/b926217b<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry');
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document.write('<li class="rss-item"><a class="rss-item" href="http://xlink.rsc.org/?DOI=b920869k&RSS=1" title="The dehydrogenase which is responsible for the stereoselective reduction of 2,5-hexanedione in bakers\' yeast was identified. Enzymatic synthesis now enables a highly efficient synthesis route to (2S,5S)-hexanediol. The high space-time yield make the proc..." target="_self">Highly efficient and stereoselective biosynthesis of (2S,5S)-hexanediol with a dehydrogenase from Saccharomyces cerevisiae</a><br />');
document.write('<p><img align=\"center\" src=\"http://www.rsc.org/ejga/OB/2010/b920869k-ga.gif\"/> </p>Marion Muller, Michael Katzberg, Martin Bertau, Werner Hummel <br/> (Paper from Org. Biomol. Chem.)<br/> Marion Muller, Org. Biomol. Chem., 2010, DOI: 10.1039/b920869k<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry');
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document.write('<li class="rss-item"><a class="rss-item" href="http://xlink.rsc.org/?DOI=b920373g&RSS=1" title="In the present study, for the first time, emphasis was placed on the investigation of the possible reaction of 2[prime or minute]-deoxyadenosine-3[prime or minute],5[prime or minute]-diphosphate radicals, leading to the formation of the related 5[prime or..." target="_self">Formation of 5[prime or minute],8-cyclo-2[prime or minute]-deoxyadenosine in single strand DNA. Theoretical quantum mechanics study</a><br />');
document.write('<p><img align=\"center\" src=\"http://www.rsc.org/ejga/OB/2010/b920373g-ga.gif\"/> </p>Boleslaw T. Karwowski <br/> (Paper from Org. Biomol. Chem.)<br/> Boleslaw T. Karwowski, Org. Biomol. Chem., 2010, DOI: 10.1039/b920373g<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry');
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document.write('<li class="rss-item"><a class="rss-item" href="http://xlink.rsc.org/?DOI=b924542a&RSS=1" title="An efficient synthesis of (+/-)-frondosin B (34% overall yield) has been developed based on the application of a Stille-Heck reaction sequence of 2-chloro-5-methoxybenzo[b]furan-3-yl triflate and 2-(3-butenyl)-3-(trimethylstannyl)cyclohex-2-enone...." target="_self">An efficient synthesis of (+/-)-frondosin B using a Stille-Heck reaction sequence</a><br />');
document.write('<p><img align=\"center\" src=\"http://www.rsc.org/ejga/OB/2010/b924542a-ga.gif\"/> </p>Kye-Simeon Masters, Bernard L. Flynn <br/> (Communication from Org. Biomol. Chem.)<br/> Kye-Simeon Masters, Org. Biomol. Chem., 2010, DOI: 10.1039/b924542a<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry');
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document.write('<li class="rss-item"><a class="rss-item" href="http://xlink.rsc.org/?DOI=b924748c&RSS=1" title="The behaviour of [small alpha]- and [small beta]-pinene in near-critical water and supercritical alcohols generated under closed-vessel conditions using a microwave was investigated, revealing significant differences in product distribution and reactivity..." target="_self">Fate of monoterpenes in near-critical water and supercritical alcohols assisted by microwave irradiation</a><br />');
document.write('<p><img align=\"center\" src=\"http://www.rsc.org/ejga/OB/2010/b924748c-ga.gif\"/> </p>Tony Szuppa, Achim Stolle, Bernd Ondruschka <br/> (Paper from Org. Biomol. Chem.)<br/> Tony Szuppa, Org. Biomol. Chem., 2010, DOI: 10.1039/b924748c<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry');
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document.write('<li class="rss-item"><a class="rss-item" href="http://xlink.rsc.org/?DOI=b920867d&RSS=1" title="A straightforward route to chiral macrocycles is described. The larger [3 + 3] macrocycles possess the right cavity size for the complexation of C60, with switchable stoichiometries in relation to the spacer shapes defining the cavities of the cyclic stru..." target="_self">Structurally-variable, rigid and optically-active D2 and D3 macrocycles possessing recognition properties towards C60</a><br />');
document.write('<p><img align=\"center\" src=\"http://www.rsc.org/ejga/OB/2010/b920867d-ga.gif\"/> </p>Carmine Coluccini, Daniele Dondi, Marco Caricato, Angelo Taglietti, Massimo Boiocchi, Dario Pasini <br/> (Paper from Org. Biomol. Chem.)<br/> Carmine Coluccini, Org. Biomol. Chem., 2010, DOI: 10.1039/b920867d<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry');
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document.write('<li class="rss-item"><a class="rss-item" href="http://xlink.rsc.org/?DOI=b923414d&RSS=1" title="Based on insights gained from a DFT study on the 6-exo-trig radical cyclization of an [small alpha],[small beta]-unsaturated ester-tethered sugar, we demonstrate that the stereoselective reaction proceeds according to a 1,4-chirality transfer mechanism...." target="_self">Unravelling the stereoselectivity in 6-exo-trig radical cyclization of [small alpha],[small beta]-unsaturated ester-tethered sugars. A tale of two stereocenters</a><br />');
document.write('<p><img align=\"center\" src=\"http://www.rsc.org/ejga/OB/2010/b923414d-ga.gif\"/> </p>Marcelo T. de Oliveira, Amary C., Daniel H. S. Leal, Maria A. F. Prado, Thais H. A. da Silva, Ricardo J. Alves <br/> (Paper from Org. Biomol. Chem.)<br/> Marcelo T. de Oliveira, Org. Biomol. Chem., 2010, DOI: 10.1039/b923414d<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry');
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document.write('<li class="rss-item"><a class="rss-item" href="http://xlink.rsc.org/?DOI=b923243e&RSS=1" title="The unprecedent pseudopericyclic [1,4]H N-to-S rearrangement of hydrazinecarbodithioate reagents, in the presence of carbon disulfide, affords thioxo-1,3,4-thiadiazolines involving a final intermolecular double S,S-transalkylation process...." target="_self">Unexpected transalkylation on 3-alkyl-2-alkylthio-1,3,4-thiadiazolium-5-thiolates: A computational and experimental mechanistic study</a><br />');
document.write('<p><img align=\"center\" src=\"http://www.rsc.org/ejga/OB/2010/b923243e-ga.gif\"/> </p>Arturo Espinosa, Rafaela Garcia, Pedro Molina, Alberto Tarraga <br/> (Paper from Org. Biomol. Chem.)<br/> Arturo Espinosa, Org. Biomol. Chem., 2010, DOI: 10.1039/b923243e<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry');
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document.write('<li class="rss-item"><a class="rss-item" href="http://xlink.rsc.org/?DOI=b921655c&RSS=1" title="Oxygen-free: Substitution of allyl halides with N-heterocyclic carbenes results in the formation of nucleophilic 1,1-diamino-1,3-dienes which are deoxy-analogues of the conceptually related Breslow-type homoenolates and exhibit significant zwitterionic ch..." target="_self">On new N-heterocyclic carbene derived alkylidene imidazolines</a><br />');
document.write('<p><img align=\"center\" src=\"http://www.rsc.org/ejga/OB/2010/b921655c-ga.gif\"/> </p>Christiane E. I. Knappke, Jorg M. Neudorfl, Axel Jacobi von Wangelin <br/> (Paper from Org. Biomol. Chem.)<br/> Christiane E. I. Knappke, Org. Biomol. Chem., 2010, DOI: 10.1039/b921655c<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry');
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document.write('<li class="rss-item"><a class="rss-item" href="http://xlink.rsc.org/?DOI=b921842d&RSS=1" title="1,2- And 1,3-cyclic sulfamidates offer a versatile and effective reactivity profile that is readily harnessed to provide a flexible entry to a wide range of substituted, functionalised and enantiomerically pure N-based heterocycles. The scope of this chem..." target="_self">N-Heterocycle construction via cyclic sulfamidates. Applications in synthesis</a><br />');
document.write('<p><img align=\"center\" src=\"http://www.rsc.org/ejga/OB/2010/b921842d-ga.gif\"/> </p>John F. Bower, Janjira Rujirawanich, Timothy Gallagher <br/> (Perspective from Org. Biomol. Chem.)<br/> John F. Bower, Org. Biomol. Chem., 2010, DOI: 10.1039/b921842d<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry');
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document.write('<li class="rss-item"><a class="rss-item" href="http://xlink.rsc.org/?DOI=b921053a&RSS=1" title="Synthesis, acid-base and photochemical properties of a new family of polyamine macrocycles containing the 2,5-diphenyl[1,3,4]oxadiazole fluorescent probe...." target="_self">New family of polyamine macrocycles containing 2,5-diphenyl[1,3,4]oxadiazole as a signaling unit. Synthesis, acid-base and spectrophotometric properties</a><br />');
document.write('<p><img align=\"center\" src=\"http://www.rsc.org/ejga/OB/2010/b921053a-ga.gif\"/> </p>Gianluca Ambrosi, Mauro Formica, Vieri Fusi, Luca Giorgi, Eleonora Macedi, Mauro Micheloni, Giovanni Piersanti, Roberto Pontellini <br/> (Paper from Org. Biomol. Chem.)<br/> Gianluca Ambrosi, Org. Biomol. Chem., 2010, DOI: 10.1039/b921053a<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry');
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document.write('<li class="rss-item"><a class="rss-item" href="http://xlink.rsc.org/?DOI=b923545k&RSS=1" title="The synthesis of oligodeoxynucleotides containing 3[prime or minute]-thionucleosides has been explored using a reverse-direction (5[prime or minute][rightward arrow]3[prime or minute]) approach, based on nucleoside monomers which contain a trityl- or dime..." target="_self">Reverse-direction (5[prime or minute][rightward arrow]3[prime or minute]) synthesis of oligonucleotides containing a 3[prime or minute]-S-phosphorothiolate linkage and 3[prime or minute]-terminal 3[prime or minute]-thionucleosides</a><br />');
document.write('<p><img align=\"center\" src=\"http://www.rsc.org/ejga/OB/2010/b923545k-ga.gif\"/> </p>James W. Gaynor, Michael M. Piperakis, Julie Fisher, Richard Cosstick <br/> (Paper from Org. Biomol. Chem.)<br/> James W. Gaynor, Org. Biomol. Chem., 2010, DOI: 10.1039/b923545k<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry');
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document.write('<li class="rss-item"><a class="rss-item" href="http://xlink.rsc.org/?DOI=b921957a&RSS=1" title="2-Oxa-5-adamantyl carbocation 4 is a viable intermediate in several SN1 reactions of 5-bromo-2-oxaadamantane but attempts to observe 4 by NMR methods failed, probably because 4 undergoes reversible ring opening to 22, which is destroyed under superacid co..." target="_self">Searching for intermediates in Prins cyclisations: the 2-oxa-5-adamantyl carbocation</a><br />');
document.write('<p><img align=\"center\" src=\"http://www.rsc.org/ejga/OB/2010/b921957a-ga.gif\"/> </p>Roger W. Alder, Fabrizio Carta, Christopher A. Reed, Irina Stoyanova, Christine L. Willis <br/> (Paper from Org. Biomol. Chem.)<br/> Roger W. Alder, Org. Biomol. Chem., 2010, DOI: 10.1039/b921957a<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry');
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document.write('<li class="rss-item"><a class="rss-item" href="http://xlink.rsc.org/?DOI=b920260a&RSS=1" title="Phenylalanine-linked pyrrolo[1,2-a]benzimidazole LL1 was successfully designed to target melanoma cells in vitro; the design utilised three molecular targets: a phenylalanine pump, the reducing enzyme DT-diaphorase, and IMP dehydrogenase...." target="_self">Triple molecular target approach to selective melanoma cytotoxicity</a><br />');
document.write('<p><img align=\"center\" src=\"http://www.rsc.org/ejga/OB/2010/b920260a-ga.gif\"/> </p>Edward B. Skibo, Akmal Jamil, Brittany Austin, Douglas Hansen, Armand Ghodousi <br/> (Paper from Org. Biomol. Chem.)<br/> Edward B. Skibo, Org. Biomol. Chem., 2010, DOI: 10.1039/b920260a<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry');
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document.write('<li class="rss-item"><a class="rss-item" href="http://xlink.rsc.org/?DOI=b923510h&RSS=1" title="In this present perspective, we summarise the recent progress on the use of gold, platinum, silver and copper complexes to activate common oxygen and nitrogen electrophiles...." target="_self">Carbo- and heterocyclisation of oxygen- and nitrogen-containing electrophiles by platinum, gold, silver and copper species</a><br />');
document.write('<p><img align=\"center\" src=\"http://www.rsc.org/ejga/OB/2010/b923510h-ga.gif\"/> </p>Arindam Das, Shariar Md. Abu Sohel, Rai-Shung Liu <br/> (Perspective from Org. Biomol. Chem.)<br/> Arindam Das, Org. Biomol. Chem., 2010, DOI: 10.1039/b923510h<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry');
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document.write('<li class="rss-item"><a class="rss-item" href="http://xlink.rsc.org/?DOI=b925494c&RSS=1" title="Enantiopure circumdatins E, H and J were prepared in 3 steps from isatoic anhydrides, l-proline and 2-nitrobenzoic acids...." target="_self">A concise synthesis of enantiopure circumdatins E, H and J</a><br />');
document.write('<p><img align=\"center\" src=\"http://www.rsc.org/ejga/OB/2010/b925494c-ga.gif\"/> </p>Paul E. Zhichkin, Xiaomin Jin, Honglu Zhang, Lisa H. Peterson, Catherine Ramirez, Tara M. Snyder, Hilde S. Burton <br/> (Communication from Org. Biomol. Chem.)<br/> Paul E. Zhichkin, Org. Biomol. Chem., 2010, DOI: 10.1039/b925494c<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry');
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document.write('<li class="rss-item"><a class="rss-item" href="http://xlink.rsc.org/?DOI=b920146g&RSS=1" title="The pillar[5]arene host forms 2:1 external complexes with alkyl-substituted paraquats, and it forms 1:1 pseudorotaxane-type inclusion complexes with methylene [-(CH2)n-] connected bis(pyridinium) derivatives...." target="_self">Complex interactions of pillar[5]arene with paraquats and bis(pyridinium) derivatives</a><br />');
document.write('<p><img align=\"center\" src=\"http://www.rsc.org/ejga/OB/2010/b920146g-ga.gif\"/> </p>Chunju Li, Qianqian Xu, Jian Li, Feina Yao, Xueshun Jia <br/> (Paper from Org. Biomol. Chem.)<br/> Chunju Li, Org. Biomol. Chem., 2010, DOI: 10.1039/b920146g<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry');
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document.write('<li class="rss-item"><a class="rss-item" href="http://xlink.rsc.org/?DOI=b921003b&RSS=1" title="High-throughput NMR titrations on H-bonded complexes were used to characterise the H-bonding properties of non-polar organic solvents, like alkanes and perfluorocarbons...." target="_self">Hydrogen bonding properties of non-polar solvents</a><br />');
document.write('<p><img align=\"center\" src=\"http://www.rsc.org/ejga/OB/2010/b921003b-ga.gif\"/> </p>Rafel Cabot, Christopher A. Hunter, Lisa M. Varley <br/> (Paper from Org. Biomol. Chem.)<br/> Rafel Cabot, Org. Biomol. Chem., 2010, DOI: 10.1039/b921003b<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry');
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document.write('<li class="rss-item"><a class="rss-item" href="http://xlink.rsc.org/?DOI=c000684j&RSS=1" title="Convenient and efficient synthesis of a novel environmentally sensitive chlorine substituted naphthalimide-based fluorophore which can be utilized for the labeling of amino acids is described...." target="_self">Synthesis and fluorescence of the new environment-sensitive fluorophore 6-chloro-2,3-naphthalimide derivative</a><br />');
document.write('<p><img align=\"center\" src=\"http://www.rsc.org/ejga/OB/2010/c000684j-ga.gif\"/> </p>Alan R. Katritzky, Sevil Ozcan, Ekaterina Todadze <br/> (Paper from Org. Biomol. Chem.)<br/> Alan R. Katritzky, Org. Biomol. Chem., 2010, DOI: 10.1039/c000684j<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry');
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document.write('<li class="rss-item"><a class="rss-item" href="http://xlink.rsc.org/?DOI=b927219b&RSS=1" title="The one-pot Horner-Wadsworth-Emmons/oxa-Michael cascade followed by spiroketalisation affords the tetracyclic benzannulated spiroketal core of berkelic acid, an extremophile natural product with selective activity against ovarian cancer...." target="_self">A flexible asymmetric synthesis of the tetracyclic core of berkelic acid using a Horner-Wadsworth-Emmons/oxa-Michael cascade</a><br />');
document.write('<p><img align=\"center\" src=\"http://www.rsc.org/ejga/OB/2010/b927219b-ga.gif\"/> </p>Zoe E. Wilson, Margaret A. Brimble <br/> (Communication from Org. Biomol. Chem.)<br/> Zoe E. Wilson, Org. Biomol. Chem., 2010, DOI: 10.1039/b927219b<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry');
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document.write('<li class="rss-item"><a class="rss-item" href="http://xlink.rsc.org/?DOI=b922442d&RSS=1" title="Enantioenriched tetrafluorinated aryl-C-nucleosides were synthesised as single diastereomers from (2R)-1-benzyloxy-4-bromo-3,3,4,4-tetrafluorobutan-2-ol. The presence of the tetrafluorinated ethylene group proved compatible with O-phosphorylation, as demo..." target="_self">Synthesis and O-phosphorylation of 3,3,4,4-tetrafluoroaryl-C-nucleoside analogues</a><br />');
document.write('<p><img align=\"center\" src=\"http://www.rsc.org/ejga/OB/2010/b922442d-ga.gif\"/> </p>Laurent Bonnac, Sarah E. Lee, Guy T. Giuffredi, Lucy M. Elphick, Alexandra A. Anderson, Emma S. Child, David J. Mann, Veronique Gouverneur <br/> (Paper from Org. Biomol. Chem.)<br/> Laurent Bonnac, Org. Biomol. Chem., 2010, DOI: 10.1039/b922442d<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry');
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document.write('<li class="rss-item"><a class="rss-item" href="http://xlink.rsc.org/?DOI=b924981h&RSS=1" title="Different experiments based on ESI-MS (competition and CID) and NMR (titration, NOESY and DOSY) were used to study the molecular recognition of N-protected amino acids and dipeptides by pseudopeptidic macrocycles...." target="_self">Molecular recognition of N-protected dipeptides by pseudopeptidic macrocycles: a comparative study of the supramolecular complexes by ESI-MS and NMR</a><br />');
document.write('<p><img align=\"center\" src=\"http://www.rsc.org/ejga/OB/2010/b924981h-ga.gif\"/> </p>Ignacio Alfonso, Michael Bolte, Miriam Bru, M. Isabel Burguete, Santiago V. Luis, Cristian Vicent <br/> (Paper from Org. Biomol. Chem.)<br/> Ignacio Alfonso, Org. Biomol. Chem., 2010, DOI: 10.1039/b924981h<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry');
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document.write('<li class="rss-item"><a class="rss-item" href="http://xlink.rsc.org/?DOI=b923253m&RSS=1" title="The carbon dioxide (CO2)-induced amidobromination of olefins with bromamine-T is described. The method can be used in reactions with a wide range of olefins, leading to the regioselective formation of amidobrominated compounds...." target="_self">CO2-induced amidobromination of olefins with bromamine-T</a><br />');
document.write('<p><img align=\"center\" src=\"http://www.rsc.org/ejga/OB/2010/b923253m-ga.gif\"/> </p>Junpei Hayakawa, Mitsuhiro Kuzuhara, Satoshi Minakata <br/> (Paper from Org. Biomol. Chem.)<br/> Junpei Hayakawa, Org. Biomol. Chem., 2010, DOI: 10.1039/b923253m<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry');
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document.write('<li class="rss-item"><a class="rss-item" href="http://xlink.rsc.org/?DOI=b921460g&RSS=1" title="Primary amino acids and their derivatives were investigated as catalysts for the direct asymmetric aldol reactions between ketones and aldehydes in the presence of water, and l-tryptophan was shown to be the best catalyst. Solvent effects, substrate scope..." target="_self">Direct asymmetric aldol reactions between aldehydes and ketones catalyzed by l-tryptophan in the presence of water</a><br />');
document.write('<p><img align=\"center\" src=\"http://www.rsc.org/ejga/OB/2010/b921460g-ga.gif\"/> </p>Zhaoqin Jiang, Hui Yang, Xiao Han, Jie Luo, Ming Wah Wong, Yixin Lu <br/> (Paper from Org. Biomol. Chem.)<br/> Zhaoqin Jiang, Org. Biomol. Chem., 2010, DOI: 10.1039/b921460g<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry');
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document.write('<li class="rss-item"><a class="rss-item" href="http://xlink.rsc.org/?DOI=b925377g&RSS=1" title="Examples of parallel interconnected kinetic asymmetric transformations are presented. In a one-pot reaction using two biocatalysts, optically active ketones, sulfoxides and sec-alcohols could concurrently be achieved in a strict parallel fashion...." target="_self">Biocatalysed concurrent production of enantioenriched compounds through parallel interconnected kinetic asymmetric transformations</a><br />');
document.write('<p><img align=\"center\" src=\"http://www.rsc.org/ejga/OB/2010/b925377g-ga.gif\"/> </p>Ana Rioz-Martinez, Fabricio R. Bisogno, Cristina Rodriguez, Gonzalo de Gonzalo, Ivan Lavandera, Daniel E. Torres Pazmino, Marco W. Fraaije, Vicente Gotor <br/> (Paper from Org. Biomol. Chem.)<br/> Ana Rioz-Martinez, Org. Biomol. Chem., 2010, DOI: 10.1039/b925377g<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry');
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document.write('<li class="rss-item"><a class="rss-item" href="http://xlink.rsc.org/?DOI=b922881k&RSS=1" title="One-electron oxidation of DNA leads to reaction at guanine because it is the nucleobase with lowest Eox. In the absence of guanine, reaction occurs primarily at TT steps. We find that remote guanines &quot;protect&quot; thymines...." target="_self">One-electron oxidation of DNA: thymine versus guanine reactivity</a><br />');
document.write('<p><img align=\"center\" src=\"http://www.rsc.org/ejga/OB/2010/b922881k-ga.gif\"/> </p>Sriram Kanvah, Gary B. Schuster <br/> (Paper from Org. Biomol. Chem.)<br/> Sriram Kanvah, Org. Biomol. Chem., 2010, DOI: 10.1039/b922881k<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry');
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document.write('<li class="rss-item"><a class="rss-item" href="http://xlink.rsc.org/?DOI=b924209k&RSS=1" title="A micro-scale, pH indicator based, colorimetric assay has been developed for the process development of transaminase catalysed reactions. Enzyme activity and stability as a function of multiple reaction parameters have been determined at 100 [small mu]L s..." target="_self">Micro-scale process development of transaminase catalysed reactions</a><br />');
document.write('<p><img align=\"center\" src=\"http://www.rsc.org/ejga/OB/2010/b924209k-ga.gif\"/> </p>Matthew D. Truppo, Nicholas J. Turner <br/> (Communication from Org. Biomol. Chem.)<br/> Matthew D. Truppo, Org. Biomol. Chem., 2010, DOI: 10.1039/b924209k<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry');
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document.write('<li class="rss-item"><a class="rss-item" href="http://xlink.rsc.org/?DOI=b920535g&RSS=1" title="Sugars and simplified oligosaccharide &quot;mimics&quot; can be joined with protein fragments at pre-defined sites and assembled into potential neoglycoprotein therapeutics using native chemical ligation...." target="_self">Exploring neoglycoprotein assembly through native chemical ligation using neoglycopeptide thioesters prepared via N[rightward arrow]S acyl transfer</a><br />');
document.write('<p><img align=\"center\" src=\"http://www.rsc.org/ejga/OB/2010/b920535g-ga.gif\"/> </p>Jonathan P. Richardson, Chung-Hei Chan, Javier Blanc, Mona Saadi, Derek Macmillan <br/> (Paper from Org. Biomol. Chem.)<br/> Jonathan P. Richardson, Org. Biomol. Chem., 2010, DOI: 10.1039/b920535g<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry');
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document.write('<li class="rss-item"><a class="rss-item" href="http://xlink.rsc.org/?DOI=b919345f&RSS=1" title="In drug discovery, structural modifications over the lead molecule are often crucial for the development of a drug. Herein, we reported the first in vivo bioisosteric effect of phosphinolactone function in relation to the lactol group constituting the bio..." target="_self">Drug discovery: phosphinolactone, in vivo bioisostere of the lactol group</a><br />');
document.write('<p><img align=\"center\" src=\"http://www.rsc.org/ejga/OB/2010/b919345f-ga.gif\"/> </p>Jean-Noel Volle, Damien Filippini, Bartlomiej Krawczy, Nikolay Kaloyanov, Arie Van der Lee, Tangui Maurice, Jean-Luc Pirat, David Virieux <br/> (Paper from Org. Biomol. Chem.)<br/> Jean-Noel Volle, Org. Biomol. Chem., 2010, DOI: 10.1039/b919345f<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry');
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document.write('<li class="rss-item"><a class="rss-item" href="http://xlink.rsc.org/?DOI=b920211k&RSS=1" title="Thymine-based nucleo-heptapeptides, containing zero, one or four Aib residues, have been synthesized. A single Aib residue is enough to increase structuration and resistance towards enzymatic degradation...." target="_self">Replacement of Ala by Aib improves structuration and biological stability in thymine-based [small alpha]-nucleopeptides</a><br />');
document.write('<p><img align=\"center\" src=\"http://www.rsc.org/ejga/OB/2010/b920211k-ga.gif\"/> </p>Piero Geotti-Bianchini, Alessandro Moretto, Cristina Peggion, Julien Beyrath, Alberto Bianco, Fernando Formaggio <br/> (Paper from Org. Biomol. Chem.)<br/> Piero Geotti-Bianchini, Org. Biomol. Chem., 2010, DOI: 10.1039/b920211k<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry');
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document.write('<li class="rss-item"><a class="rss-item" href="http://xlink.rsc.org/?DOI=b925962g&RSS=1" title="A series of thiourea-amine bifunctional catalysts have been developed by a rational combination of prolines with cinchona alkaloids, which are found to be highly efficient catalysts for the conjugate addition of ketones/aldehydes to a wide range of nitroa..." target="_self">Novel thiourea-amine bifunctional catalysts for asymmetric conjugate addition of ketones/aldehydes to nitroalkenes: rational structural combination for high catalytic efficiency</a><br />');
document.write('<p><img align=\"center\" src=\"http://www.rsc.org/ejga/OB/2010/b925962g-ga.gif\"/> </p>Jia-Rong Chen, Yi-Ju Cao, You-Quan Zou, Fen Tan, Liang Fu, Xiao-Yu Zhu, Wen-Jing Xiao <br/> (Communication from Org. Biomol. Chem.)<br/> Jia-Rong Chen, Org. Biomol. Chem., 2010, DOI: 10.1039/b925962g<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry');
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document.write('<li class="rss-item"><a class="rss-item" href="http://xlink.rsc.org/?DOI=b921545j&RSS=1" title="The cis-dihydrodiol metabolite from methyl benzoate has been used as a synthetic precursor of carba-[small beta]-l-galactopyranose, carba-[small beta]-l-talopyranose, carba-[small alpha]-l-talopyranose and carba-[small beta]-l-galactopyranose...." target="_self">Chemoenzymatic synthesis of the carbasugars carba-[small beta]-l-galactopyranose, carba-[small beta]-l-talopyranose and carba-[small alpha]-l-talopyranose from methyl benzoate</a><br />');
document.write('<p><img align=\"center\" src=\"http://www.rsc.org/ejga/OB/2010/b921545j-ga.gif\"/> </p>Derek R. Boyd, Narain D. Sharma, Nigel I. Bowers, Gerard B. Coen, John F. Malone, Colin R. O\'Dowd, Paul J. Stevenson, Christopher C. R. Allen <br/> (Paper from Org. Biomol. Chem.)<br/> Derek R. Boyd, Org. Biomol. Chem., 2010, DOI: 10.1039/b921545j<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry');
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document.write('<li class="rss-item"><a class="rss-item" href="http://xlink.rsc.org/?DOI=b921694d&RSS=1" title="Radical intermediates occurring during endoperoxide formation were trapped and the spin adducts were characterised by both EPR and tandem mass spectrometry...." target="_self">A combined spin trapping/EPR/mass spectrometry approach to study the formation of a cyclic peroxide by dienolic precursor autoxidation</a><br />');
document.write('<p><img align=\"center\" src=\"http://www.rsc.org/ejga/OB/2010/b921694d-ga.gif\"/> </p>Mathilde Triquigneaux, Laurence Charles, Christiane Andre-Barres, Beatrice Tuccio <br/> (Paper from Org. Biomol. Chem.)<br/> Mathilde Triquigneaux, Org. Biomol. Chem., 2010, DOI: 10.1039/b921694d<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry');
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document.write('<li class="rss-item"><a class="rss-item" href="http://xlink.rsc.org/?DOI=b924272d&RSS=1" title="A general method for the one-pot, three-component Strecker reaction of ketones, amines and trimethylsilyl cyanide was developed using Bronsted acids as organocatalysts to afford [small alpha]-aminonitriles in good to excellent yields...." target="_self">Bronsted acid-catalyzed efficient Strecker reaction of ketones, amines and trimethylsilyl cyanide</a><br />');
document.write('<p><img align=\"center\" src=\"http://www.rsc.org/ejga/OB/2010/b924272d-ga.gif\"/> </p>Guang-Wu Zhang, Dong-Hua Zheng, Jing Nie, Teng Wang, Jun-An Ma <br/> (Paper from Org. Biomol. Chem.)<br/> Guang-Wu Zhang, Org. Biomol. Chem., 2010, DOI: 10.1039/b924272d<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry');
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document.write('<li class="rss-item"><a class="rss-item" href="http://xlink.rsc.org/?DOI=b920670a&RSS=1" title="Triple-helical peptides (THPs) have been utilized as collagen models since the 1960s. In the last two decades, virtually all aspects of collagen structural biochemistry have been explored with THP models...." target="_self">Synthesis and biological applications of collagen-model triple-helical peptides</a><br />');
document.write('<p><img align=\"center\" src=\"http://www.rsc.org/ejga/OB/2010/b920670a-ga.gif\"/> </p>Gregg B. Fields <br/> (Perspective from Org. Biomol. Chem.)<br/> Gregg B. Fields, Org. Biomol. Chem., 2010, DOI: 10.1039/b920670a<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry');
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document.write('<li class="rss-item"><a class="rss-item" href="http://xlink.rsc.org/?DOI=b921232a&RSS=1" title="1,5 triazole derivatives bind to tRNALys3 with similar affinity but different selectivity than their corresponding 1,4 isomers...." target="_self">Tether influence on the binding properties of tRNALys3 ligands designed by a fragment-based approach</a><br />');
document.write('<p><img align=\"center\" src=\"http://www.rsc.org/ejga/OB/2010/b921232a-ga.gif\"/> </p>Roba Moumne, Valery Larue, Bili Seijo, Thomas Lecourt, Laurent Micouin, Carine Tisne <br/> (Paper from Org. Biomol. Chem.)<br/> Roba Moumne, Org. Biomol. Chem., 2010, DOI: 10.1039/b921232a<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry');
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document.write('<li class="rss-item"><a class="rss-item" href="http://xlink.rsc.org/?DOI=b924619c&RSS=1" title="Functionalized arene diazonium tetrafluoroborates are obtained from acetamides in a convenient one-flask procedure. A diazonium salt obtained via this method was used in the synthesis of the natural product de-O-methyl centrolobine...." target="_self">Functionalized alkoxy arene diazonium salts from paracetamol</a><br />');
document.write('<p><img align=\"center\" src=\"http://www.rsc.org/ejga/OB/2010/b924619c-ga.gif\"/> </p>Bernd Schmidt, Rene Berger, Frank Holter <br/> (Paper from Org. Biomol. Chem.)<br/> Bernd Schmidt, Org. Biomol. Chem., 2010, DOI: 10.1039/b924619c<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry');
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document.write('<li class="rss-item"><a class="rss-item" href="http://xlink.rsc.org/?DOI=b924015b&RSS=1" title="A coumarin-thiourea conjugate (1) behaves as a highly selective fluorescent probe for Hg2+ in aqueous media with a broad pH range, 2-12...." target="_self">A coumarin-thiourea conjugate as a fluorescent probe for Hg(ii) in aqueous media with a broad pH range 2-12</a><br />');
document.write('<p><img align=\"center\" src=\"http://www.rsc.org/ejga/OB/2010/b924015b-ga.gif\"/> </p>Yasuhiro Shiraishi, Shigehiro Sumiya, Takayuki Hirai <br/> (Paper from Org. Biomol. Chem.)<br/> Yasuhiro Shiraishi, Org. Biomol. Chem., 2010, DOI: 10.1039/b924015b<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry');
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document.write('<li class="rss-item"><a class="rss-item" href="http://xlink.rsc.org/?DOI=b924560j&RSS=1" title="UV-B photoirradiation of serotonin, tryptophan and tyrosine with oxygen results in DNA cleavage by generation of reactive oxygen species as demonstrated by agarose gel electrophoresis with pBR 322 DNA...." target="_self">Photoinduced DNA cleavage by formation of ROS from oxygen with a neurotransmitter and aromatic amino acids</a><br />');
document.write('<p><img align=\"center\" src=\"http://www.rsc.org/ejga/OB/2010/b924560j-ga.gif\"/> </p>Tomonori Kawashima, Kei Ohkubo, Shunichi Fukuzumi <br/> (Communication from Org. Biomol. Chem.)<br/> Tomonori Kawashima, Org. Biomol. Chem., 2010, DOI: 10.1039/b924560j<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry');
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document.write('<li class="rss-item"><a class="rss-item" href="http://xlink.rsc.org/?DOI=b918005b&RSS=1" title="[5,6] Open fulleroids were found to display a more enhanced and regioselective Diels-Alder addition at the bridgehead anti-Bredt double bond as compared with [6,6] closed methanofullerene and C60...." target="_self">Kinetics and regioselectivity in the Diels-Alder reaction of fulleroids vs. methanofullerene and C60</a><br />');
document.write('<p><img align=\"center\" src=\"http://www.rsc.org/ejga/OB/2010/b918005b-ga.gif\"/> </p>Naohiko Ikuma, Yasunori Susami, Takumi Oshima <br/> (Paper from Org. Biomol. Chem.)<br/> Naohiko Ikuma, Org. Biomol. Chem., 2010, DOI: 10.1039/b918005b<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry');
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document.write('<li class="rss-item"><a class="rss-item" href="http://xlink.rsc.org/?DOI=b917188f&RSS=1" title="Components of synthetic organic photosystems that are not integrated into supramolecular n/p-heterojunctions are shown to generate weak photocurrents only, whereas SHJ-compatible components are operational in the same system...." target="_self">Optoelectronically mismatched oligophenylethynyl-naphthalenediimide SHJ architectures</a><br />');
document.write('<p><img align=\"center\" src=\"http://www.rsc.org/ejga/OB/2010/b917188f-ga.gif\"/> </p>Santanu Maity, Rajesh Bhosale, Natalie Banerji, Eric Vauthey, Naomi Sakai, Stefan Matile <br/> (Paper from Org. Biomol. Chem.)<br/> Santanu Maity, Org. Biomol. Chem., 2010, DOI: 10.1039/b917188f<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry');
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document.write('<li class="rss-item"><a class="rss-item" href="http://xlink.rsc.org/?DOI=b924072a&RSS=1" title="Sonogashira cross-couplings of halogenated nucleosides and nucleoside triphosphates with bile-acid acetylenes gave steroid-nucleos(t)ide conjugates that were incorporated to DNA by polymerase...." target="_self">Synthesis of nucleoside and nucleotide conjugates of bile acids, and polymerase construction of bile acid-functionalized DNA</a><br />');
document.write('<p><img align=\"center\" src=\"http://www.rsc.org/ejga/OB/2010/b924072a-ga.gif\"/> </p>Satu Ikonen, Hana Macickova-Cahova, Radek Pohl, Miloslav Sanda, Michal Hocek <br/> (Paper from Org. Biomol. Chem.)<br/> Satu Ikonen, Org. Biomol. Chem., 2010, DOI: 10.1039/b924072a<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry');
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document.write('<li class="rss-item"><a class="rss-item" href="http://xlink.rsc.org/?DOI=b922730j&RSS=1" title="A DFT computational study of two pericyclic reactions is reported. The computational calculations represent a very useful tool to study separately the occurrence of thermal and non-thermal effects of microwave irradiation...." target="_self">Computational calculations in microwave-assisted organic synthesis (MAOS). Application to cycloaddition reactions</a><br />');
document.write('<p><img align=\"center\" src=\"http://www.rsc.org/ejga/OB/2010/b922730j-ga.gif\"/> </p>A. de Cozar, M. C. Millan, C. Cebrian, P. Prieto, A. Diaz-Ortiz, A. de la Hoz, F. P. Cossio <br/> (Paper from Org. Biomol. Chem.)<br/> A. de Cozar, Org. Biomol. Chem., 2010, DOI: 10.1039/b922730j<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry');
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document.write('<li class="rss-item"><a class="rss-item" href="http://xlink.rsc.org/?DOI=b921385f&RSS=1" title="It is possible to use water-miscible organic solvents in DNA-based asymmetric catalysis without affecting the enantioselectivity of the reactions. Additionally, it enables the use of higher substrate concentrations and lower temperatures, which gives rise..." target="_self">Organic co-solvents in aqueous DNA-based asymmetric catalysis</a><br />');
document.write('<p><img align=\"center\" src=\"http://www.rsc.org/ejga/OB/2010/b921385f-ga.gif\"/> </p>Rik P. Megens, Gerard Roelfes <br/> (Paper from Org. Biomol. Chem.)<br/> Rik P. Megens, Org. Biomol. Chem., 2010, DOI: 10.1039/b921385f<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry');
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document.write('<li class="rss-item"><a class="rss-item" href="http://xlink.rsc.org/?DOI=b920285d&RSS=1" title="For the first time a synthesis of (4E,8E,10E)-9-methyl-4,8,10-sphingatrienine, the acid-labile core component of marine sphingolipids, has been achieved using a fragment linkage strategy based on copper-mediated 1,2-metallate rearrangements. A related syn..." target="_self">Synthesis of phalluside-1 and Sch II using 1,2-metallate rearrangements</a><br />');
document.write('<p><img align=\"center\" src=\"http://www.rsc.org/ejga/OB/2010/b920285d-ga.gif\"/> </p>Fiona J. Black, Philip J. Kocienski <br/> (Paper from Org. Biomol. Chem.)<br/> Fiona J. Black, Org. Biomol. Chem., 2010, DOI: 10.1039/b920285d<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry');
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document.write('<li class="rss-item"><a class="rss-item" href="http://xlink.rsc.org/?DOI=b920058d&RSS=1" title="Zinc porphyrin functionalized with l-glutamide has been newly synthesized and its unique responses such as ligand-specific induction of secondary chirality thorough the aggregation morphology change are reported...." target="_self">Versatile chiroptics of peptide-induced assemblies of metalloporphyrins</a><br />');
document.write('<p><img align=\"center\" src=\"http://www.rsc.org/ejga/OB/2010/b920058d-ga.gif\"/> </p>Hirokuni Jintoku, Takashi Sagawa, Tsuyoshi Sawada, Makoto Takafuji, Hirotaka Ihara <br/> (Paper from Org. Biomol. Chem.)<br/> Hirokuni Jintoku, Org. Biomol. Chem., 2010, DOI: 10.1039/b920058d<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry');
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document.write('<li class="rss-item"><a class="rss-item" href="http://xlink.rsc.org/?DOI=b920861e&RSS=1" title="3-Amidoindoles were synthesized from commercially available arylhydrazines and propargylamines over Zn-salt mediated one pot procedure in excellent regioselectivity and up to 94% yield...." target="_self">A new facile synthesis of 3-amidoindole derivatives and their evaluation as potential GSK-3[small beta] inhibitors</a><br />');
document.write('<p><img align=\"center\" src=\"http://www.rsc.org/ejga/OB/2010/b920861e-ga.gif\"/> </p>Anahit Pews-Davtyan, Annegret Tillack, Anne-Caroline Schmole, Stefanie Ortinau, Moritz J. Frech, Arndt Rolfs, Matthias Beller <br/> (Paper from Org. Biomol. Chem.)<br/> Anahit Pews-Davtyan, Org. Biomol. Chem., 2010, DOI: 10.1039/b920861e<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry');
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document.write('<li class="rss-item"><a class="rss-item" href="http://xlink.rsc.org/?DOI=b917280g&RSS=1" title="The total synthesis and in vitro biological properties of a new series of multimeric porphyrin-NLS conjugates bearing two, three or four peptides with the minimum sequence PKKKRKV are described. The mono- and di-substituted photosensitizers bearing one or..." target="_self">Influence of the number and distribution of NLS peptides on the photosensitizing activity of multimeric porphyrin-NLS</a><br />');
document.write('<p><img align=\"center\" src=\"http://www.rsc.org/ejga/OB/2010/b917280g-ga.gif\"/> </p>Martha Sibrian-Vazquez, Timothy J. Jensen, M. Graca H. Vicente <br/> (Paper from Org. Biomol. Chem.)<br/> Martha Sibrian-Vazquez, Org. Biomol. Chem., 2010, DOI: 10.1039/b917280g<br/> To cite this article before page numbers are assigned, use the DOI form of citation above. <br/>The content of this RSS Feed (c) The Royal Society of Chemistry');
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