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<?xml-stylesheet type="text/xsl" media="screen" href="/~d/styles/rss2full.xsl"?><?xml-stylesheet type="text/css" media="screen" href="http://feeds.rsc.org/~d/styles/itemcontent.css"?><rss xmlns:a10="http://www.w3.org/2005/Atom" xmlns:feedburner="http://rssnamespace.org/feedburner/ext/1.0" version="2.0"><channel><title>RSC - Chem. Soc. Rev. latest articles</title><link>http://pubs.rsc.org/en/Journals/Journal/CS</link><description>RSC - Chem. Soc. Rev. latest articles</description><copyright>Copyright (c)  The Royal Society of Chemistry</copyright><lastBuildDate>Fri, 24 May 2013 12:44:37 Z</lastBuildDate><category>RSC - Chem. Soc. Rev. latest articles</category><image><url>http://pubs.rsc.org/content/NewImages/rsc_publishing_logo.gif</url><title>RSC - Chem. Soc. Rev. latest articles</title><link>http://pubs.rsc.org/en/Journals/Journal/CS</link></image><atom10:link xmlns:atom10="http://www.w3.org/2005/Atom" rel="self" type="application/rss+xml" href="http://feeds.rsc.org/rss/CS" /><feedburner:info uri="rss/cs" /><atom10:link xmlns:atom10="http://www.w3.org/2005/Atom" rel="hub" href="http://pubsubhubbub.appspot.com/" /><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60069F"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60069F</guid><link>http://feeds.rsc.org/~r/rss/CS/~3/xlbPnoYV0mg/C3CS60069F</link><title>Supramolecular complexations of natural products</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3CS60069F" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Soc. Rev.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3CS60069F, Review Article&lt;/div&gt;&lt;div&gt;Hans-Jorg Schneider, Pawan Agrawal, Anatoly K. Yatsimirsky&lt;br/&gt;Synthetic host compounds can efficiently complex natural products, such as a modified cyclodextrin with a bile acid or a cucurbituril with a peptide; they may be used &lt;em&gt;e.g.&lt;/em&gt; for sensing, separation, enzyme assays, or drug protection. Also the host properties of some natural products find applications in analysis and separation.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/CS/~4/xlbPnoYV0mg" height="1" width="1"/&gt;</description><a10:updated>2013-05-24T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Hans-Jorg Schneider</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Pawan Agrawal</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Anatoly K. Yatsimirsky</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60069F</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60055F"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60055F</guid><link>http://feeds.rsc.org/~r/rss/CS/~3/XLqf1LfzAWA/C3CS60055F</link><title>Thiol-addition reactions and their applications in thiol recognition</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3CS60055F" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Soc. Rev.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3CS60055F, Review Article&lt;/div&gt;&lt;div&gt;Caixia Yin, Fangjun Huo, Jingjing Zhang, Ramon Martinez-Manez, Yutao Yang, Haigang Lv, Sidian Li&lt;br/&gt;Four reaction types, including 1,1, 1,2, 1,3, 1,4 addition reactions, based on different Michael acceptors have been used for the chromo-fluorogenic recognition of thiols.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/CS/~4/XLqf1LfzAWA" height="1" width="1"/&gt;</description><a10:updated>2013-05-23T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Caixia Yin</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Fangjun Huo</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jingjing Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ramon Martinez-Manez</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yutao Yang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Haigang Lv</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sidian Li</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60055F</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60024F"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60024F</guid><link>http://feeds.rsc.org/~r/rss/CS/~3/vJbWqQm4I-M/C3CS60024F</link><title>Recent progress in luminescent and colorimetric chemosensors for detection of thiols</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3CS60024F" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Soc. Rev.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3CS60024F, Tutorial Review&lt;/div&gt;&lt;div&gt;Hyo Sung Jung, Xiaoqiang Chen, Jong Seung Kim, Juyoung Yoon&lt;br/&gt;This review focuses on the recent examples of fluorescent or colorimetric sensors for thiols, categorizing them based on diverse sensing mechanisms of optical probes towards thiols.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/CS/~4/vJbWqQm4I-M" height="1" width="1"/&gt;</description><a10:updated>2013-05-20T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Hyo Sung Jung</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiaoqiang Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jong Seung Kim</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Juyoung Yoon</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60024F</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60050E"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60050E</guid><link>http://feeds.rsc.org/~r/rss/CS/~3/3IFOqVkAa8s/C3CS60050E</link><title>Chemical information matters: an e-Research perspective on information and data sharing in the chemical sciences</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3CS60050E" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Soc. Rev.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3CS60050E, Review Article&lt;/div&gt;&lt;div&gt;Colin L. Bird, Jeremy G. Frey&lt;br/&gt;A timely review of the information data sharing issue highlighted by the recent report about the research practices of chemists.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/CS/~4/3IFOqVkAa8s" height="1" width="1"/&gt;</description><a10:updated>2013-05-20T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Colin L. Bird</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jeremy G. Frey</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60050E</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60132C"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60132C</guid><link>http://feeds.rsc.org/~r/rss/CS/~3/CPL30aWG2EQ/C3CS60132C</link><title>Graphane and hydrogenated graphene</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3CS60132C" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Soc. Rev.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3CS60132C, Tutorial Review&lt;/div&gt;&lt;div&gt;Martin Pumera, Colin Hong An Wong&lt;br/&gt;Do graphane and partially hydrogenated graphane possess the predicted properties? How to make graphane? What is graphane in the first place? Read here!&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/CS/~4/CPL30aWG2EQ" height="1" width="1"/&gt;</description><a10:updated>2013-05-20T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Martin Pumera</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Colin Hong An Wong</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60132C</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS35494F"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS35494F</guid><link>http://feeds.rsc.org/~r/rss/CS/~3/Rp-MhZ-QO68/C3CS35494F</link><title>Mechanochemistry of fullerenes and related materials</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3CS35494F" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Soc. Rev.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3CS35494F, Review Article&lt;/div&gt;&lt;div&gt;San-E Zhu, Fei Li, Guan-Wu Wang&lt;br/&gt;Functionalizations of fullerenes and related materials have been achieved by ball milling and hand grinding.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/CS/~4/Rp-MhZ-QO68" height="1" width="1"/&gt;</description><a10:updated>2013-05-16T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">San-E Zhu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Fei Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Guan-Wu Wang</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS35494F</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60031A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60031A</guid><link>http://feeds.rsc.org/~r/rss/CS/~3/ohFNypWk0yI/C3CS60031A</link><title>Responsive hydrogels - structurally and dimensionally optimized smart frameworks for applications in catalysis, micro-system technology and material science</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3CS60031A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Soc. Rev.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3CS60031A, Review Article&lt;/div&gt;&lt;div&gt;Artjom Doring, Wolfgang Birnbaum, Dirk Kuckling&lt;br/&gt;The review covers the most recent developments in the field of responsive hydrogels focussing on catalysis, sensors and actuators.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/CS/~4/ohFNypWk0yI" height="1" width="1"/&gt;</description><a10:updated>2013-05-15T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Artjom Doring</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Wolfgang Birnbaum</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Dirk Kuckling</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60031A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60105F"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60105F</guid><link>http://feeds.rsc.org/~r/rss/CS/~3/Slrlf5X5hOk/C3CS60105F</link><title>The modern interpretation of the Wittig reaction mechanism</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3CS60105F" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Soc. Rev.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3CS60105F, Review Article&lt;/div&gt;&lt;div&gt;Peter A. Byrne, Declan G. Gilheany&lt;br/&gt;Li salt-free Wittig reactions of all ylide types occur under kinetic control, and by a common [2+2] cycloaddition mechanism in which oxaphosphetane is the first-formed and only intermediate.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/CS/~4/Slrlf5X5hOk" height="1" width="1"/&gt;</description><a10:updated>2013-05-14T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Peter A. Byrne</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Declan G. Gilheany</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60105F</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS35526H"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS35526H</guid><link>http://feeds.rsc.org/~r/rss/CS/~3/HoA_MeRZV-Q/C3CS35526H</link><title>Mechanochemical organic synthesis</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3CS35526H" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Soc. Rev.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3CS35526H, Review Article&lt;/div&gt;&lt;div&gt;Guan-Wu Wang&lt;br/&gt;Various solvent-free mechanochemical organic reactions can be realized by ball milling techniques.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/CS/~4/HoA_MeRZV-Q" height="1" width="1"/&gt;</description><a10:updated>2013-05-09T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Guan-Wu Wang</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS35526H</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS35532B"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS35532B</guid><link>http://feeds.rsc.org/~r/rss/CS/~3/8JlZ8wSDvIU/C3CS35532B</link><title>Application of mass spectrometric techniques to delineate the modes-of-action of anticancer metallodrugs</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3CS35532B" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Soc. Rev.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3CS35532B, Review Article&lt;/div&gt;&lt;div&gt;Christian G. Hartinger, Michael Groessl, Samuel M. Meier, Angela Casini, Paul J. Dyson&lt;br/&gt;Mass spectrometric methods are increasingly being used to help elucidate the modes of action of metal-based anticancer agents. Nascent developments and recent applications are discussed in this review.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/CS/~4/8JlZ8wSDvIU" height="1" width="1"/&gt;</description><a10:updated>2013-05-09T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Christian G. Hartinger</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Michael Groessl</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Samuel M. Meier</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Angela Casini</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Paul J. Dyson</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS35532B</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60113G"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60113G</guid><link>http://feeds.rsc.org/~r/rss/CS/~3/aPYyPCMZ0MM/C3CS60113G</link><title>Chemical routes to top-down nanofabrication</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3CS60113G" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Soc. Rev.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3CS60113G, Tutorial Review&lt;/div&gt;&lt;div&gt;Hai-Dong Yu, Michelle D. Regulacio, Enyi Ye, Ming-Yong Han&lt;br/&gt;This tutorial review summarizes the different chemical routes to top-down nanofabrication that have enabled the construction of three-dimensional nanostructures with unique structural features and promising applications.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/CS/~4/aPYyPCMZ0MM" height="1" width="1"/&gt;</description><a10:updated>2013-05-08T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Hai-Dong Yu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Michelle D. Regulacio</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Enyi Ye</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ming-Yong Han</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60113G</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60029G"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60029G</guid><link>http://feeds.rsc.org/~r/rss/CS/~3/UrDm7IJKpeA/C3CS60029G</link><title>Near-infrared phosphorescence: materials and applications</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3CS60029G" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Soc. Rev.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3CS60029G, Review Article&lt;/div&gt;&lt;div&gt;Haifeng Xiang, Jinghui Cheng, Xiaofeng Ma, Xiangge Zhou, Jason Joseph Chruma&lt;br/&gt;An overview of the latest developments and applications in the field of room-temperature near-infrared phosphorescent transition-metal complexes is given.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/CS/~4/UrDm7IJKpeA" height="1" width="1"/&gt;</description><a10:updated>2013-05-07T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Haifeng Xiang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jinghui Cheng</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiaofeng Ma</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiangge Zhou</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jason Joseph Chruma</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60029G</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60076A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60076A</guid><link>http://feeds.rsc.org/~r/rss/CS/~3/h_V6_3uPTPk/C3CS60076A</link><title>From powder to technical body: the undervalued science of catalyst scale up</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3CS60076A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Soc. Rev.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3CS60076A, Review Article&lt;/div&gt;&lt;div&gt;Sharon Mitchell, Nina-Luisa Michels, Javier Perez-Ramirez&lt;br/&gt;This review examines the complexity associated with the scale up of heterogeneous catalysts, proposing directions to strengthen the fundamental understanding of this exciting, but often neglected field.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/CS/~4/h_V6_3uPTPk" height="1" width="1"/&gt;</description><a10:updated>2013-05-07T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Sharon Mitchell</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Nina-Luisa Michels</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Javier Perez-Ramirez</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60076A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS90029K"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS90029K</guid><link>http://feeds.rsc.org/~r/rss/CS/~3/dm3tLuAiwfI/C3CS90029K</link><title>Multivalent scaffolds in glycoscience: an overview</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3CS90029K" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Soc. Rev.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;42&lt;/b&gt;,4515-4517&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3CS90029K, Editorial&lt;/div&gt;&lt;div&gt;Olivier Renaudet, Rene Roy&lt;br/&gt;Guest editors Olivier Renaudet and Rene Roy introduce the Multivalent scaffolds in glycosciences themed issue of &lt;em&gt;Chemical Society Reviews&lt;/em&gt;.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/CS/~4/dm3tLuAiwfI" height="1" width="1"/&gt;</description><a10:updated>2013-04-30T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Olivier Renaudet</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Rene Roy</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS90029K</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60090D"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60090D</guid><link>http://feeds.rsc.org/~r/rss/CS/~3/iM6SlPzzK78/C3CS60090D</link><title>How do multivalent glycodendrimers benefit from sulfur chemistry?</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3CS60090D" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Soc. Rev.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;42&lt;/b&gt;,4823-4841&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3CS60090D, Review Article&lt;/div&gt;&lt;div&gt;Marc Gingras, Yoann M. Chabre, Myriam Roy, Rene Roy&lt;br/&gt;The combination of sugar and sulfur chemistry is reported to benefit multivalent glycodendrimer chemistry. Besides the contribution of sulfur to structural linking strategies, we emphasized some novelties in the modulation of optoelectronic properties of those ligands and their uses in glycobiology, in materials science and in nanoscience.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/CS/~4/iM6SlPzzK78" height="1" width="1"/&gt;</description><a10:updated>2013-04-30T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Marc Gingras</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yoann M. Chabre</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Myriam Roy</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Rene Roy</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60090D</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS00001J"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS00001J</guid><link>http://feeds.rsc.org/~r/rss/CS/~3/750i5Wzror0/C3CS00001J</link><title>Multivalent glycoliposomes and micelles to study carbohydrate-protein and carbohydrate-carbohydrate interactions</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3CS00001J" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Soc. Rev.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;42&lt;/b&gt;,4640-4656&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3CS00001J, Tutorial Review&lt;/div&gt;&lt;div&gt;Narayanaswamy Jayaraman, Krishnagopal Maiti, Kottari Naresh&lt;br/&gt;The synthetic design of glycolipids, and formation of glycoliposomes and micelles thereof to study multivalent carbohydrate-protein and carbohydrate-carbohydrate interactions are presented.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/CS/~4/750i5Wzror0" height="1" width="1"/&gt;</description><a10:updated>2013-03-13T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Narayanaswamy Jayaraman</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Krishnagopal Maiti</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Kottari Naresh</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS00001J</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS35483K"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS35483K</guid><link>http://feeds.rsc.org/~r/rss/CS/~3/BKnXMzWAOOQ/C3CS35483K</link><title>Multivalent glycoconjugate syntheses and applications using aromatic scaffolds</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3CS35483K" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Soc. Rev.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;42&lt;/b&gt;,4657-4708&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3CS35483K, Review Article&lt;/div&gt;&lt;div&gt;Yoann M. Chabre, Rene Roy&lt;br/&gt;This review describes the chemical syntheses and biological properties of multivalent glycoarchitectures prepared around aromatic backbones.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/CS/~4/BKnXMzWAOOQ" height="1" width="1"/&gt;</description><a10:updated>2013-02-12T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Yoann M. Chabre</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Rene Roy</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS35483K</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS35504G"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS35504G</guid><link>http://feeds.rsc.org/~r/rss/CS/~3/pWSKk6P2egI/C3CS35504G</link><title>Glycopeptide dendrimers as Pseudomonas aeruginosa biofilm inhibitors</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3CS35504G" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Soc. Rev.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;42&lt;/b&gt;,4814-4822&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3CS35504G, Review Article&lt;/div&gt;&lt;div&gt;Jean-Louis Reymond, Myriam Bergmann, Tamis Darbre&lt;br/&gt;Inhibition and dispersal of &lt;em&gt;Pseudomonas aeruginosa&lt;/em&gt; biofilms were achieved with multivalent glycopeptide dendrimer inhibitors of lectins LecA and LecB.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/CS/~4/pWSKk6P2egI" height="1" width="1"/&gt;</description><a10:updated>2013-02-01T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Jean-Louis Reymond</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Myriam Bergmann</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Tamis Darbre</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS35504G</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C2CS35437C"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C2CS35437C</guid><link>http://feeds.rsc.org/~r/rss/CS/~3/Dkfmo_kfRTg/C2CS35437C</link><title>Multivalent glycocalixarenes for recognition of biological macromolecules: glycocalyx mimics capable of multitasking</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C2CS35437C" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Soc. Rev.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;42&lt;/b&gt;,4623-4639&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2CS35437C, Tutorial Review&lt;/div&gt;&lt;div&gt;Francesco Sansone, Alessandro Casnati&lt;br/&gt;Glycocalixarenes, like the cell-wall glycocalyx, recognise macromolecules through multivalency. Their possibility to simultaneously perform other tasks such as drug-delivery, imaging or immunostimulation suggests their potential application in bionanotechnology and nanomedicine.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/CS/~4/Dkfmo_kfRTg" height="1" width="1"/&gt;</description><a10:updated>2013-01-29T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Francesco Sansone</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Alessandro Casnati</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C2CS35437C</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C2CS35435G"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C2CS35435G</guid><link>http://feeds.rsc.org/~r/rss/CS/~3/NUbqsIBXa3w/C2CS35435G</link><title>Binding sugars: from natural lectins to synthetic receptors and engineered neolectins</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C2CS35435G" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Soc. Rev.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;42&lt;/b&gt;,4798-4813&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2CS35435G, Review Article&lt;/div&gt;&lt;div&gt;Julie Arnaud, Aymeric Audfray, Anne Imberty&lt;br/&gt;From structural knowledge of natural lectins, artificial carbohydrate-binders are developed based either on engineered biomolecules or on biomimetics systems.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/CS/~4/NUbqsIBXa3w" height="1" width="1"/&gt;</description><a10:updated>2013-01-25T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Julie Arnaud</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Aymeric Audfray</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Anne Imberty</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C2CS35435G</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C2CS35395D"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C2CS35395D</guid><link>http://feeds.rsc.org/~r/rss/CS/~3/woJAUwmf3UM/C2CS35395D</link><title>Enzymatic glycosylation of multivalent scaffolds</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C2CS35395D" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Soc. Rev.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;42&lt;/b&gt;,4774-4797&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2CS35395D, Review Article&lt;/div&gt;&lt;div&gt;Pavla Bojarova, Ruben R. Rosencrantz, Lothar Elling, Vladimir Kren&lt;br/&gt;The use of glycosyltransferases for glycosylating natural and synthetic multivalent substrates is presented, including glycoarrays, metabolic labeling and glycosylation engineering.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/CS/~4/woJAUwmf3UM" height="1" width="1"/&gt;</description><a10:updated>2013-01-24T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Pavla Bojarova</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ruben R. Rosencrantz</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lothar Elling</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Vladimir Kren</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C2CS35395D</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C2CS35424A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C2CS35424A</guid><link>http://feeds.rsc.org/~r/rss/CS/~3/_tSeTVaG5XA/C2CS35424A</link><title>Cyclodextrin-based multivalent glycodisplays: covalent and supramolecular conjugates to assess carbohydrate-protein interactions</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C2CS35424A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Soc. Rev.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;42&lt;/b&gt;,4746-4773&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2CS35424A, Review Article&lt;/div&gt;&lt;div&gt;Alvaro Martinez, Carmen Ortiz Mellet, Jose M. Garcia Fernandez&lt;br/&gt;Multivalent cyclodextrin conjugates, from covalent to self-assembled constructs, can be tailored to investigate and control carbohydrate binding to biological receptors.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/CS/~4/_tSeTVaG5XA" height="1" width="1"/&gt;</description><a10:updated>2013-01-23T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Alvaro Martinez</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Carmen Ortiz Mellet</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jose M. Garcia Fernandez</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C2CS35424A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C2CS35420A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C2CS35420A</guid><link>http://feeds.rsc.org/~r/rss/CS/~3/a81kCxHrljQ/C2CS35420A</link><title>Glyconanoparticles as multifunctional and multimodal carbohydrate systems</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C2CS35420A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Soc. Rev.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;42&lt;/b&gt;,4728-4745&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2CS35420A, Review Article&lt;/div&gt;&lt;div&gt;Marco Marradi, Fabrizio Chiodo, Isabel Garcia, Soledad Penades&lt;br/&gt;Glyconanoparticles with varying density of carbohydrates are multivalent and multifunctional tools for studying interactions, for developing vaccines, and for molecular imaging.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/CS/~4/a81kCxHrljQ" height="1" width="1"/&gt;</description><a10:updated>2013-01-04T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Marco Marradi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Fabrizio Chiodo</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Isabel Garcia</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Soledad Penades</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C2CS35420A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C2CS35430F"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C2CS35430F</guid><link>http://feeds.rsc.org/~r/rss/CS/~3/v0j35s8acFA/C2CS35430F</link><title>Bacterial toxin inhibitors based on multivalent scaffolds</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C2CS35430F" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Soc. Rev.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;42&lt;/b&gt;,4613-4622&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2CS35430F, Tutorial Review&lt;/div&gt;&lt;div&gt;Thomas R. Branson, W. Bruce Turnbull&lt;br/&gt;Protein toxins released by certain intestinal bacteria are the cause of many diarrhoeal diseases including cholera and travellers' diarrhoea.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/CS/~4/v0j35s8acFA" height="1" width="1"/&gt;</description><a10:updated>2012-12-21T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Thomas R. Branson</creator><creator xmlns="http://purl.org/dc/elements/1.1/">W. Bruce Turnbull</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C2CS35430F</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C2CS35413F"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C2CS35413F</guid><link>http://feeds.rsc.org/~r/rss/CS/~3/dyqvo7yHdCs/C2CS35413F</link><title>Multivalent glyco(cyclo)peptides</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C2CS35413F" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Soc. Rev.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;42&lt;/b&gt;,4599-4612&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2CS35413F, Tutorial Review&lt;/div&gt;&lt;div&gt;M. Carmen Galan, Pascal Dumy, Olivier Renaudet&lt;br/&gt;This tutorial review provides an overview of the most recent advances in the preparation and utilization of glycopeptides and glycocyclopeptides in glycobiology.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/CS/~4/dyqvo7yHdCs" height="1" width="1"/&gt;</description><a10:updated>2012-12-21T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">M. Carmen Galan</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Pascal Dumy</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Olivier Renaudet</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C2CS35413F</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C2CS35421G"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C2CS35421G</guid><link>http://feeds.rsc.org/~r/rss/CS/~3/gW5CSYusbI4/C2CS35421G</link><title>Carbosilane glycodendrimers</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C2CS35421G" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Soc. Rev.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;42&lt;/b&gt;,4574-4598&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2CS35421G, Tutorial Review&lt;/div&gt;&lt;div&gt;Ken Hatano, Koji Matsuoka, Daiyo Terunuma&lt;br/&gt;Glycodendrimers fascinate both carbohydrate chemists and biologists because of their ability to recognize lectins and enhance carbohydrate-protein interactions.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/CS/~4/gW5CSYusbI4" height="1" width="1"/&gt;</description><a10:updated>2012-12-21T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Ken Hatano</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Koji Matsuoka</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Daiyo Terunuma</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C2CS35421G</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C2CS35406C"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C2CS35406C</guid><link>http://feeds.rsc.org/~r/rss/CS/~3/zZv_ps0HtVk/C2CS35406C</link><title>Glycoclusters on oligonucleotide and PNA scaffolds: synthesis and applications</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C2CS35406C" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Soc. Rev.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;42&lt;/b&gt;,4557-4573&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2CS35406C, Tutorial Review&lt;/div&gt;&lt;div&gt;Nicolas Spinelli, Eric Defrancq, Francois Morvan&lt;br/&gt;Oligonucleotide glycocluster conjugates are involved in several approaches for cellular delivery, carbohydrate microarray or supramolecular glycoclusters.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/CS/~4/zZv_ps0HtVk" height="1" width="1"/&gt;</description><a10:updated>2012-12-19T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Nicolas Spinelli</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Eric Defrancq</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Francois Morvan</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C2CS35406C</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C2CS35408J"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C2CS35408J</guid><link>http://feeds.rsc.org/~r/rss/CS/~3/Zvh2p7iiSL4/C2CS35408J</link><title>Multivalent glycoconjugates as anti-pathogenic agents</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C2CS35408J" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Soc. Rev.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;42&lt;/b&gt;,4709-4727&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2CS35408J, Review Article&lt;/div&gt;&lt;div&gt;Anna Bernardi, Jesus Jimenez-Barbero, Alessandro Casnati, Cristina De Castro, Tamis Darbre, Franck Fieschi, Jukka Finne, Horst Funken, Karl-Erich Jaeger, Martina Lahmann, Thisbe K. Lindhorst, Marco Marradi, Paul Messner, Antonio Molinaro, Paul V. Murphy, Cristina Nativi, Stefan Oscarson, Soledad Penades, Francesco Peri, Roland J. Pieters, Olivier Renaudet, Jean-Louis Reymond, Barbara Richichi, Javier Rojo, Francesco Sansone, Christina Schaffer, W. Bruce Turnbull, Trinidad Velasco-Torrijos, Sebastien Vidal, Stephane Vincent, Tom Wennekes, Han Zuilhof, Anne Imberty&lt;br/&gt;Glycocompounds interfere with infection and immunity.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/CS/~4/Zvh2p7iiSL4" height="1" width="1"/&gt;</description><a10:updated>2012-12-19T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Anna Bernardi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jesus Jimenez-Barbero</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Alessandro Casnati</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Cristina De Castro</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Tamis Darbre</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Franck Fieschi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jukka Finne</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Horst Funken</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Karl-Erich Jaeger</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Martina Lahmann</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Thisbe K. Lindhorst</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Marco Marradi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Paul Messner</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Antonio Molinaro</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Paul V. Murphy</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Cristina Nativi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Stefan Oscarson</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Soledad Penades</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Francesco Peri</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Roland J. Pieters</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Olivier Renaudet</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jean-Louis Reymond</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Barbara Richichi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Javier Rojo</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Francesco Sansone</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Christina Schaffer</creator><creator xmlns="http://purl.org/dc/elements/1.1/">W. Bruce Turnbull</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Trinidad Velasco-Torrijos</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sebastien Vidal</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Stephane Vincent</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Tom Wennekes</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Han Zuilhof</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Anne Imberty</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C2CS35408J</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C2CS35422E"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C2CS35422E</guid><link>http://feeds.rsc.org/~r/rss/CS/~3/REvpm4YaQkg/C2CS35422E</link><title>Clustered carbohydrates in synthetic vaccines</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C2CS35422E" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Soc. Rev.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;42&lt;/b&gt;,4543-4556&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2CS35422E, Tutorial Review&lt;/div&gt;&lt;div&gt;Francesco Peri&lt;br/&gt;Are there general rules for the design of efficient carbohydrate vaccines? Recent achievements in the field of carbohydrate immunization.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/CS/~4/REvpm4YaQkg" height="1" width="1"/&gt;</description><a10:updated>2012-12-18T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Francesco Peri</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C2CS35422E</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C2CS35396B"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C2CS35396B</guid><link>http://feeds.rsc.org/~r/rss/CS/~3/4yRt-FT8fVI/C2CS35396B</link><title>Sweet carbon nanostructures: carbohydrate conjugates with carbon nanotubes and graphene and their applications</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C2CS35396B" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Soc. Rev.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;42&lt;/b&gt;,4532-4542&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2CS35396B, Tutorial Review&lt;/div&gt;&lt;div&gt;Yanan Chen, Alexander Star, Sebastien Vidal&lt;br/&gt;This review highlights the strategies for the covalent and noncovalent functionalization of carbon nanostructures with carbohydrates and applications in biology.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/CS/~4/4yRt-FT8fVI" height="1" width="1"/&gt;</description><a10:updated>2012-12-17T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Yanan Chen</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Alexander Star</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sebastien Vidal</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C2CS35396B</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C2CS35219B"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C2CS35219B</guid><link>http://feeds.rsc.org/~r/rss/CS/~3/v4Wjkx8bk9w/C2CS35219B</link><title>Multivalency in heterogeneous glycoenvironments: hetero-glycoclusters, -glycopolymers and -glycoassemblies</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C2CS35219B" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Soc. Rev.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;42&lt;/b&gt;,4518-4531&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2CS35219B, Tutorial Review&lt;/div&gt;&lt;div&gt;Jose L. Jimenez Blanco, Carmen Ortiz Mellet, Jose M. Garcia Fernandez&lt;br/&gt;"Shuffled", multidomain and fluidic displays of different glycotopes allow assessing the effect of heterogeneity in carbohydrate-lectin or -antibody interactions.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/CS/~4/v4Wjkx8bk9w" height="1" width="1"/&gt;</description><a10:updated>2012-08-21T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Jose L. Jimenez Blanco</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Carmen Ortiz Mellet</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jose M. Garcia Fernandez</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C2CS35219B</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60053J"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60053J</guid><link>http://feeds.rsc.org/~r/rss/CS/~3/Ofwkm7bgVDo/C3CS60053J</link><title>Alkaline polymer electrolyte membranes for fuel cell applications</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3CS60053J" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Soc. Rev.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3CS60053J, Review Article&lt;/div&gt;&lt;div&gt;Yan-Jie Wang, Jinli Qiao, Ryan Baker, Jiujun Zhang&lt;br/&gt;In this review, we examine the most recent progress in the area of alkaline polymer electrolyte membrane (PEM) development in terms of material selection, synthesis, characterization, and theoretical approach, as well as their fabrication into alkaline PEM-based membrane electrode assemblies and the corresponding fuel cell performance.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/CS/~4/Ofwkm7bgVDo" height="1" width="1"/&gt;</description><a10:updated>2013-05-02T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Yan-Jie Wang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jinli Qiao</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ryan Baker</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jiujun Zhang</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60053J</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60058K"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60058K</guid><link>http://feeds.rsc.org/~r/rss/CS/~3/7zaXsEsBJhA/C3CS60058K</link><title>Magnetic responsive polymer composite materials</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3CS60058K" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Soc. Rev.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3CS60058K, Tutorial Review&lt;/div&gt;&lt;div&gt;Julie Thevenot, Hugo Oliveira, Olivier Sandre, Sebastien Lecommandoux&lt;br/&gt;Magnetic responsive materials and their potential breakthrough applications in the biomedical, coatings, microfluidics and microelectronics fields are highlighted in this review.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/CS/~4/7zaXsEsBJhA" height="1" width="1"/&gt;</description><a10:updated>2013-05-02T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Julie Thevenot</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hugo Oliveira</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Olivier Sandre</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Sebastien Lecommandoux</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60058K</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60063G"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60063G</guid><link>http://feeds.rsc.org/~r/rss/CS/~3/t1ohX6abN1s/C3CS60063G</link><title>Stimuli responsive synthetic polypeptides derived from N-carboxyanhydride (NCA) polymerisation</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3CS60063G" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Soc. Rev.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3CS60063G, Review Article&lt;/div&gt;&lt;div&gt;Jin Huang, Andreas Heise&lt;br/&gt;Advanced polymerisation and modification approaches have opened new avenues to produce novel biologically inspired responsive synthetic polypeptides.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/CS/~4/t1ohX6abN1s" height="1" width="1"/&gt;</description><a10:updated>2013-05-01T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Jin Huang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Andreas Heise</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60063G</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60081E"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60081E</guid><link>http://feeds.rsc.org/~r/rss/CS/~3/A2XQEU5F2qQ/C3CS60081E</link><title>Proteotyping for the rapid identification of influenza virus and other biopathogens</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3CS60081E" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Soc. Rev.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3CS60081E, Tutorial Review&lt;/div&gt;&lt;div&gt;Kevin M. Downard&lt;br/&gt;A new proteotyping approach to characterise the influenza virus, and by extension other biopathogens, through the detection of signature peptides.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/CS/~4/A2XQEU5F2qQ" height="1" width="1"/&gt;</description><a10:updated>2013-04-30T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Kevin M. Downard</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60081E</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60119F"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60119F</guid><link>http://feeds.rsc.org/~r/rss/CS/~3/6VGfVIKDc8Q/C3CS60119F</link><title>Ubiquitous trisulfur radical anion: fundamentals and applications in materials science, electrochemistry, analytical chemistry and geochemistry</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3CS60119F" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Soc. Rev.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3CS60119F, Tutorial Review&lt;/div&gt;&lt;div&gt;Tristram Chivers, Philip J. W. Elder&lt;br/&gt;The fundamental chemistry and multi-faceted influence of the paramagnetic, deep blue sulfur species [S&lt;small&gt;&lt;sub&gt;3&lt;/sub&gt;&lt;/small&gt;][radical dot]&lt;small&gt;&lt;sup&gt;-&lt;/sup&gt;&lt;/small&gt; in materials science, electrochemistry, analytical chemistry and geochemistry are discussed.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/CS/~4/6VGfVIKDc8Q" height="1" width="1"/&gt;</description><a10:updated>2013-04-30T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Tristram Chivers</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Philip J. W. Elder</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60119F</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60101C"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60101C</guid><link>http://feeds.rsc.org/~r/rss/CS/~3/dmoUc-KtVdI/C3CS60101C</link><title>Dendritic architectures based on bis-MPA: functional polymeric scaffolds for application-driven research</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3CS60101C" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Soc. Rev.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3CS60101C, Review Article&lt;/div&gt;&lt;div&gt;Anna Carlmark, Eva Malmstrom, Michael Malkoch&lt;br/&gt;This review covers the array of synthetic methodologies as well as potential applications of dendritic architectures based on bis-MPA.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/CS/~4/dmoUc-KtVdI" height="1" width="1"/&gt;</description><a10:updated>2013-04-30T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Anna Carlmark</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Eva Malmstrom</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Michael Malkoch</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60101C</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60074B"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60074B</guid><link>http://feeds.rsc.org/~r/rss/CS/~3/8j24lWtqNtc/C3CS60074B</link><title>An overview of the magnetoresistance phenomenon in molecular systems</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3CS60074B" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Soc. Rev.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3CS60074B, Review Article&lt;/div&gt;&lt;div&gt;Hongbo Gu, Xi Zhang, Huige Wei, Yudong Huang, Suying Wei, Zhanhu Guo&lt;br/&gt;Magnetoresistance effects in molecular systems are summarized and the related models are reviewed together with some detailed application examples.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/CS/~4/8j24lWtqNtc" height="1" width="1"/&gt;</description><a10:updated>2013-04-30T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Hongbo Gu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xi Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Huige Wei</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yudong Huang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Suying Wei</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhanhu Guo</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60074B</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60108K"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60108K</guid><link>http://feeds.rsc.org/~r/rss/CS/~3/8oGa1S6HDcM/C3CS60108K</link><title>Heteroarenes as high performance organic semiconductors</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3CS60108K" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Soc. Rev.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3CS60108K, Review Article&lt;/div&gt;&lt;div&gt;Wei Jiang, Yan Li, Zhaohui Wang&lt;br/&gt;This review article highlights the practical synthesis, tuneable self-assembled packing arrangement and high electronic performance of heteroarenes.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/CS/~4/8oGa1S6HDcM" height="1" width="1"/&gt;</description><a10:updated>2013-04-29T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Wei Jiang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yan Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Zhaohui Wang</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60108K</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS90030D"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS90030D</guid><link>http://feeds.rsc.org/~r/rss/CS/~3/fwg9aMjUVME/C3CS90030D</link><title>Carbohydrate chemistry</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3CS90030D" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Soc. Rev.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;42&lt;/b&gt;,4267-4269&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3CS90030D, Editorial&lt;/div&gt;&lt;div&gt;Injae Shin, Kwan Soo Kim&lt;br/&gt;Guest editors Injae Shin and Kwan Soo Kim introduce the Carbohydrate chemistry themed issue of &lt;em&gt;Chemical Society Reviews&lt;/em&gt;.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/CS/~4/fwg9aMjUVME" height="1" width="1"/&gt;</description><a10:updated>2013-04-19T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Injae Shin</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Kwan Soo Kim</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS90030D</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60089K"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60089K</guid><link>http://feeds.rsc.org/~r/rss/CS/~3/l8lhTHhAP1U/C3CS60089K</link><title>Bridging lectin binding sites by multivalent carbohydrates</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3CS60089K" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Soc. Rev.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;42&lt;/b&gt;,4492-4503&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3CS60089K, Review Article&lt;/div&gt;&lt;div&gt;Valentin Wittmann, Roland J. Pieters&lt;br/&gt;Creating potent bridging ligands for medicinally important lectins is a strategy that increasingly sees creative and successful examples that are highlighted here.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/CS/~4/l8lhTHhAP1U" height="1" width="1"/&gt;</description><a10:updated>2013-04-19T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Valentin Wittmann</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Roland J. Pieters</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60089K</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60097A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60097A</guid><link>http://feeds.rsc.org/~r/rss/CS/~3/HzYtZc1K7vM/C3CS60097A</link><title>Glycopolymer probes of signal transduction</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3CS60097A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Soc. Rev.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;42&lt;/b&gt;,4476-4491&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3CS60097A, Review Article&lt;/div&gt;&lt;div&gt;Laura L. Kiessling, Joseph C. Grim&lt;br/&gt;This review begins with an overview of the structural features of glycopolymers that can affect their recognition by protein receptors and then highlights the use of glycopolymers as probes of signal transduction.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/CS/~4/HzYtZc1K7vM" height="1" width="1"/&gt;</description><a10:updated>2013-04-18T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Laura L. Kiessling</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Joseph C. Grim</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60097A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60056D"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60056D</guid><link>http://feeds.rsc.org/~r/rss/CS/~3/nKmFTLSeVFg/C3CS60056D</link><title>Development of fucosyltransferase and fucosidase inhibitors</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3CS60056D" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Soc. Rev.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;42&lt;/b&gt;,4459-4475&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3CS60056D, Review Article&lt;/div&gt;&lt;div&gt;Zhijay Tu, Yu-Nong Lin, Chun-Hung Lin&lt;br/&gt;We provide an updated review of the development of fucosyltransferase and fucosidase inhibitors with an emphasis on the structure-activity relationship.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/CS/~4/nKmFTLSeVFg" height="1" width="1"/&gt;</description><a10:updated>2013-04-15T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Zhijay Tu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yu-Nong Lin</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Chun-Hung Lin</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60056D</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS35419A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS35419A</guid><link>http://feeds.rsc.org/~r/rss/CS/~3/PZvQ-pWdQek/C3CS35419A</link><title>Lectin microarrays: concept, principle and applications</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3CS35419A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Soc. Rev.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;42&lt;/b&gt;,4443-4458&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3CS35419A, Review Article&lt;/div&gt;&lt;div&gt;Jun Hirabayashi, Masao Yamada, Atsushi Kuno, Hiroaki Tateno&lt;br/&gt;The lectin microarray is a novel technology that enables rapid and high-sensitivity profiling of complex features of glycans without their liberation.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/CS/~4/PZvQ-pWdQek" height="1" width="1"/&gt;</description><a10:updated>2013-02-26T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Jun Hirabayashi</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Masao Yamada</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Atsushi Kuno</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hiroaki Tateno</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS35419A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS35470A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS35470A</guid><link>http://feeds.rsc.org/~r/rss/CS/~3/zbAp9e6U2kQ/C3CS35470A</link><title>The development of synthetic antitumour vaccines from mucin glycopeptide antigens</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3CS35470A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Soc. Rev.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;42&lt;/b&gt;,4421-4442&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3CS35470A, Review Article&lt;/div&gt;&lt;div&gt;Nikola Gaidzik, Ulrika Westerlind, Horst Kunz&lt;br/&gt;Synthetic vaccines containing glycopeptide antigens from tumour-associated mucins and immunostimulatory components induce strong immune responses directed towards tumour cells.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/CS/~4/zbAp9e6U2kQ" height="1" width="1"/&gt;</description><a10:updated>2013-02-25T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Nikola Gaidzik</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ulrika Westerlind</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Horst Kunz</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS35470A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS35485G"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS35485G</guid><link>http://feeds.rsc.org/~r/rss/CS/~3/FZ2Y0GqM4qk/C3CS35485G</link><title>Chemical assembly of N-glycoproteins: a refined toolbox to address a ubiquitous posttranslational modification</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3CS35485G" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Soc. Rev.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;42&lt;/b&gt;,4408-4420&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3CS35485G, Review Article&lt;/div&gt;&lt;div&gt;Carlo Unverzagt, Yasuhiro Kajihara&lt;br/&gt;Recent developments in the ligation chemistry of peptides and carbohydrates have enabled researchers to assemble entire glycoproteins with high precision.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/CS/~4/FZ2Y0GqM4qk" height="1" width="1"/&gt;</description><a10:updated>2013-02-13T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Carlo Unverzagt</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yasuhiro Kajihara</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS35485G</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS35457A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS35457A</guid><link>http://feeds.rsc.org/~r/rss/CS/~3/VHR8aGo3vSo/C3CS35457A</link><title>Design of chemical glycosyl donors: does changing ring conformation influence selectivity/reactivity?</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3CS35457A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Soc. Rev.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;42&lt;/b&gt;,4297-4309&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3CS35457A, Tutorial Review&lt;/div&gt;&lt;div&gt;Hiroko Satoh, Shino Manabe&lt;br/&gt;This &lt;em&gt;tutorial review&lt;/em&gt; focuses on the design of glycosyl donors, especially on attempts to control selectivity/reactivity by employing bulky substituents, cyclic protecting groups, or bridged structures.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/CS/~4/VHR8aGo3vSo" height="1" width="1"/&gt;</description><a10:updated>2013-01-30T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Hiroko Satoh</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Shino Manabe</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS35457A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C2CS35438A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C2CS35438A</guid><link>http://feeds.rsc.org/~r/rss/CS/~3/3V52o4bQo-E/C2CS35438A</link><title>The biosynthesis of nitrogen-, sulfur-, and high-carbon chain-containing sugars</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C2CS35438A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Soc. Rev.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;42&lt;/b&gt;,4377-4407&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2CS35438A, Review Article&lt;/div&gt;&lt;div&gt;Chia-I. Lin, Reid M. McCarty, Hung-wen Liu&lt;br/&gt;This review provides an update of current understanding of the biosynthesis of nitrogen-, sulfur-, high-carbon chain-containing sugars.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/CS/~4/3V52o4bQo-E" height="1" width="1"/&gt;</description><a10:updated>2013-01-25T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Chia-I. Lin</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Reid M. McCarty</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Hung-wen Liu</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C2CS35438A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C2CS35427F"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C2CS35427F</guid><link>http://feeds.rsc.org/~r/rss/CS/~3/1GX3ym9TzIs/C2CS35427F</link><title>Glyconanotechnology</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C2CS35427F" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Soc. Rev.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;42&lt;/b&gt;,4358-4376&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2CS35427F, Review Article&lt;/div&gt;&lt;div&gt;Niels C. Reichardt, Manuel Martin-Lomas, Soledad Penades&lt;br/&gt;The most recent developments of glyconanomaterials for drug design, vaccine development, molecular imaging, enzyme inhibition and biosensors are critically discussed.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/CS/~4/1GX3ym9TzIs" height="1" width="1"/&gt;</description><a10:updated>2013-01-10T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Niels C. Reichardt</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Manuel Martin-Lomas</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Soledad Penades</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C2CS35427F</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C2CS35416K"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C2CS35416K</guid><link>http://feeds.rsc.org/~r/rss/CS/~3/Gqxy6VSYJoQ/C2CS35416K</link><title>Chemical probing of glycans in cells and organisms</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C2CS35416K" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Soc. Rev.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;42&lt;/b&gt;,4284-4296&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2CS35416K, Tutorial Review&lt;/div&gt;&lt;div&gt;Sara H. Rouhanifard, Lars Ulrik Nordstrom, Tianqing Zheng, Peng Wu&lt;br/&gt;New chemical tools have made it possible to probe glycans in living systems.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/CS/~4/Gqxy6VSYJoQ" height="1" width="1"/&gt;</description><a10:updated>2012-12-21T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Sara H. Rouhanifard</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Lars Ulrik Nordstrom</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Tianqing Zheng</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Peng Wu</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C2CS35416K</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C2CS35412H"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C2CS35412H</guid><link>http://feeds.rsc.org/~r/rss/CS/~3/dVWKM2HxUXk/C2CS35412H</link><title>Chemical approaches to study O-GlcNAcylation</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C2CS35412H" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Soc. Rev.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;42&lt;/b&gt;,4345-4357&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2CS35412H, Review Article&lt;/div&gt;&lt;div&gt;Partha S. Banerjee, Gerald W. Hart, Jin Won Cho&lt;br/&gt;The chemistry of O-GlcNAc, the cycling enzymes and some of the methods developed to study protein O-GlcNAc modifications are described.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/CS/~4/dVWKM2HxUXk" height="1" width="1"/&gt;</description><a10:updated>2012-12-18T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Partha S. Banerjee</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Gerald W. Hart</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jin Won Cho</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C2CS35412H</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C2CS35382B"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C2CS35382B</guid><link>http://feeds.rsc.org/~r/rss/CS/~3/ngKvrPryDXw/C2CS35382B</link><title>Designing a new antifungal glycoconjugate vaccine</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C2CS35382B" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Soc. Rev.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;42&lt;/b&gt;,4327-4344&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2CS35382B, Review Article&lt;/div&gt;&lt;div&gt;Margaret A. Johnson, David R. Bundle&lt;br/&gt;New strategies for binding site mapping and for eliciting protective immune responses against small carbohydrate epitopes are reviewed.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/CS/~4/ngKvrPryDXw" height="1" width="1"/&gt;</description><a10:updated>2012-12-11T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Margaret A. Johnson</creator><creator xmlns="http://purl.org/dc/elements/1.1/">David R. Bundle</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C2CS35382B</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C2CS35403A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C2CS35403A</guid><link>http://feeds.rsc.org/~r/rss/CS/~3/zvZPXOJyIv4/C2CS35403A</link><title>Fluoro-C-glycosides and fluoro-carbasugars, hydrolytically stable and synthetically challenging glycomimetics</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C2CS35403A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Soc. Rev.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;42&lt;/b&gt;,4270-4283&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2CS35403A, Tutorial Review&lt;/div&gt;&lt;div&gt;Eric Leclerc, Xavier Pannecoucke, Melanie Etheve-Quelquejeu, Matthieu Sollogoub&lt;br/&gt;Fluoro-C-glycosides and fluoro-carbasugars are a particular subclass of hydrolytically stable glycomimetics that are expected to have different, hopefully improved properties thanks to the stereoelectronic features of the fluoroalkyl moiety.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/CS/~4/zvZPXOJyIv4" height="1" width="1"/&gt;</description><a10:updated>2012-12-04T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Eric Leclerc</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xavier Pannecoucke</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Melanie Etheve-Quelquejeu</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Matthieu Sollogoub</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C2CS35403A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C2CS35401B"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C2CS35401B</guid><link>http://feeds.rsc.org/~r/rss/CS/~3/29LKWjKvbp4/C2CS35401B</link><title>Carbohydrate microarrays</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C2CS35401B" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Soc. Rev.&lt;/b&gt;&lt;/i&gt;, 2013, &lt;b&gt;42&lt;/b&gt;,4310-4326&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2CS35401B, Review Article&lt;/div&gt;&lt;div&gt;Sungjin Park, Jeffrey C. Gildersleeve, Ola Blixt, Injae Shin&lt;br/&gt;This article discusses construction of carbohydrate microarrays, detection methods of carbohydrate microarrays and their applications in biological and biomedical research.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/CS/~4/29LKWjKvbp4" height="1" width="1"/&gt;</description><a10:updated>2012-11-28T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Sungjin Park</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jeffrey C. Gildersleeve</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ola Blixt</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Injae Shin</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C2CS35401B</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS35515B"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS35515B</guid><link>http://feeds.rsc.org/~r/rss/CS/~3/F2ZfLIzrM-c/C3CS35515B</link><title>Microfluidics and Raman microscopy: current applications and future challenges</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3CS35515B" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Soc. Rev.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3CS35515B, Review Article&lt;/div&gt;&lt;div&gt;Adam F. Chrimes, Khashayar Khoshmanesh, Paul R. Stoddart, Arnan Mitchell, Kourosh Kalantar-zadeh&lt;br/&gt;This critical review discusses the integration of Raman microscopy with microfluidics - its methods and applications.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/CS/~4/F2ZfLIzrM-c" height="1" width="1"/&gt;</description><a10:updated>2013-04-26T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Adam F. Chrimes</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Khashayar Khoshmanesh</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Paul R. Stoddart</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Arnan Mitchell</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Kourosh Kalantar-zadeh</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS35515B</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60045A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60045A</guid><link>http://feeds.rsc.org/~r/rss/CS/~3/fqsTa5qQZUk/C3CS60045A</link><title>Adaptive all the way down: Building responsive materials from hierarchies of chemomechanical feedback</title><description>&lt;div&gt;&lt;p&gt;&lt;img align="center"  src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C3CS60045A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Chem. Soc. Rev.&lt;/b&gt;&lt;/i&gt;, 2013, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3CS60045A, Tutorial Review&lt;/div&gt;&lt;div&gt;Alison Grinthal, Joanna Aizenberg&lt;br/&gt;We explore how feedback between chemistry and motion can be harnessed to design an unlimited diversity of multi-responsive, multifunctional systems with adaptiveness built in from the bottom up.&lt;br/&gt;To cite this article before page numbers are assigned, use the DOI form of citation above.&lt;br/&gt;The content of this RSS Feed (c) The Royal Society of Chemistry&lt;/div&gt;&lt;img src="http://feeds.feedburner.com/~r/rss/CS/~4/fqsTa5qQZUk" height="1" width="1"/&gt;</description><a10:updated>2013-04-26T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Alison Grinthal</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Joanna Aizenberg</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/CS/C3CS60045A</feedburner:origLink></item></channel></rss>
