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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 - Nat. Prod. Rep. latest articles</title><link>http://pubs.rsc.org/en/Journals/Journal/NP</link><description>RSC - Nat. Prod. Rep. latest articles</description><copyright>Copyright (c)  The Royal Society of Chemistry</copyright><lastBuildDate>Tue, 14 Feb 2012 03:03:20 Z</lastBuildDate><category>RSC - Nat. Prod. Rep. latest articles</category><image><url>http://pubs.rsc.org/content/NewImages/rsc_publishing_logo.gif</url><title>RSC - Nat. Prod. Rep. latest articles</title><link>http://pubs.rsc.org/en/Journals/Journal/NP</link></image><atom10:link xmlns:atom10="http://www.w3.org/2005/Atom" rel="self" type="application/rss+xml" href="http://feeds.rsc.org/rss/NP" /><feedburner:info uri="rss/np" /><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/2012/NP/C2NP00078D"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/NP/C2NP00078D</guid><link>http://feeds.rsc.org/~r/rss/NP/~3/7Pl_2bDQdgU/C2NP00078D</link><title>Electrophilic and nucleophilic enzymatic cascade reactions in biosynthesis</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=C2NP00078D" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Nat. Prod. Rep.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2NP00078D, Review&lt;/div&gt;&lt;div&gt;Barbara T. Ueberbacher, Melanie Hall, Kurt Faber&lt;br/&gt;Cyclic terpenoids and polyethers are formed &lt;i&gt;via&lt;/i&gt; enzyme-initiated cascade reactions for ring formation, which proceed either &lt;i&gt;via&lt;/i&gt; electrophilic (cationic) or nucleophilic (anionic) pathways through (i) triggering of the cascade ('initiation'), (ii) 'proliferation' of the cyclization and (iii) 'termination' of the cascade.&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/NP/~4/7Pl_2bDQdgU" height="1" width="1"/&gt;</description><a10:updated>2012-02-03T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Barbara T. Ueberbacher</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Melanie Hall</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Kurt Faber</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/NP/C2NP00078D</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/NP/C2NP00065B"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/NP/C2NP00065B</guid><link>http://feeds.rsc.org/~r/rss/NP/~3/3ZjaUOQAvzc/C2NP00065B</link><title>Didemnins, tamandarins and related 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=C2NP00065B" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Nat. Prod. Rep.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2NP00065B, Review&lt;/div&gt;&lt;div&gt;Jisun Lee, Judith N. Currano, Patrick J. Carroll, Madeleine M. Joullie&lt;br/&gt;This review highlights the long-standing study of didemnins and its critical application towards the understanding of the molecular mechanism of action of tamandarins and their potential use as therapeutic agents.&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/NP/~4/3ZjaUOQAvzc" height="1" width="1"/&gt;</description><a10:updated>2012-01-23T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Jisun Lee</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Judith N. Currano</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Patrick J. Carroll</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Madeleine M. Joullie</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/NP/C2NP00065B</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/NP/C2NP00088A"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/NP/C2NP00088A</guid><link>http://feeds.rsc.org/~r/rss/NP/~3/ikU3aVm-2Rg/C2NP00088A</link><title>Triptolide: structural modifications, structure-activity relationships, bioactivities, clinical development and mechanisms</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=C2NP00088A" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Nat. Prod. Rep.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2NP00088A, Review&lt;/div&gt;&lt;div&gt;Zhao-Li Zhou, Ya-Xi Yang, Jian Ding, Yuan-Chao Li, Ze-Hong Miao&lt;br/&gt;This review covers research efforts of the last forty years, focusing on the structural modifications, structure-activity relationships, pharmacology and clinical development of triptolide, a principal bioactive ingredient of &lt;i&gt;Tripterygium wilfordii&lt;/i&gt; Hook F.&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/NP/~4/ikU3aVm-2Rg" height="1" width="1"/&gt;</description><a10:updated>2012-01-23T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Zhao-Li Zhou</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ya-Xi Yang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jian Ding</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Yuan-Chao Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Ze-Hong Miao</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/NP/C2NP00088A</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2012/NP/C2NP00073C"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2012/NP/C2NP00073C</guid><link>http://feeds.rsc.org/~r/rss/NP/~3/cxlEAofAIv4/C2NP00073C</link><title>The taxonomy, biology and chemistry of the fungal Pestalotiopsis genus</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=C2NP00073C" /&gt;&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;i&gt;&lt;b&gt;Nat. Prod. Rep.&lt;/b&gt;&lt;/i&gt;, 2012, Advance Article&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C2NP00073C, Review&lt;/div&gt;&lt;div&gt;Xiao-Long Yang, Jing-Ze Zhang, Du-Qiang Luo&lt;br/&gt;A growing body of evidence indicates that the &lt;i&gt;Pestalotiopsis&lt;/i&gt; genus represents a huge and largely untapped resource of bioactive metabolites. This review systematically surveys the taxonomy, biology and chemistry of the &lt;i&gt;Pestalotiopsis&lt;/i&gt; genus. It also summarises the biosynthetic relationships and chemical synthesis of secondary metabolites.&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/NP/~4/cxlEAofAIv4" height="1" width="1"/&gt;</description><a10:updated>2012-01-17T00:00:00Z</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Xiao-Long Yang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Jing-Ze Zhang</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Du-Qiang Luo</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2012/NP/C2NP00073C</feedburner:origLink></item></channel></rss>

