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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>Fri, 24 May 2013 09:46:13 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/2013/NP/C3NP90015K"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NP/C3NP90015K</guid><link>http://feeds.rsc.org/~r/rss/NP/~3/rxibbcmCTXs/C3NP90015K</link><title>Hot off the press</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=C3NP90015K" /&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;, 2013, &lt;b&gt;30&lt;/b&gt;,760-764&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NP90015K, Hot off the Press Article&lt;/div&gt;&lt;div&gt;Robert A. Hill, Andrew Sutherland&lt;br/&gt;A personal selection of 33 recent papers is presented covering various aspects of current developments in bioorganic chemistry and novel natural products such as asperterpenoid A, a metabolite of an endophytic &lt;em&gt;Aspergillus&lt;/em&gt; species.&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/rxibbcmCTXs" 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/">Robert A. Hill</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Andrew Sutherland</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NP/C3NP90015K</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NP/C3NP70003H"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NP/C3NP70003H</guid><link>http://feeds.rsc.org/~r/rss/NP/~3/E1v0JCJX46k/C3NP70003H</link><title>Glucuronides from metabolites to medicines: a survey of the in vivo generation, chemical synthesis and properties of glucuronides</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=C3NP70003H" /&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;, 2013, &lt;b&gt;30&lt;/b&gt;,806-848&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NP70003H, Review Article&lt;/div&gt;&lt;div&gt;Andrew V. Stachulski, Xiaoli Meng&lt;br/&gt;Glucuronides have long been known as important phase 2 metabolites of drug molecules. Here we review and update the biogenesis, chemical synthesis and bio-medicinal chemistry of glucuronides, including their potential as drugs and pro-drugs and their interaction with biomolecules.&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/E1v0JCJX46k" 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/">Andrew V. Stachulski</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Xiaoli Meng</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NP/C3NP70003H</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NP/C3NP70006B"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NP/C3NP70006B</guid><link>http://feeds.rsc.org/~r/rss/NP/~3/O9IbWKKh-Ts/C3NP70006B</link><title>Muscarine, imidaozle, oxazole and thiazole alkaloids</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=C3NP70006B" /&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;, 2013, &lt;b&gt;30&lt;/b&gt;,869-915&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NP70006B, Review Article&lt;/div&gt;&lt;div&gt;Zhong Jin&lt;br/&gt;This review summarizes the latest progress on the isolation, identification, biological activities, and chemical synthesis of these NPs with a literature coverage from July 2010 to June 2012.&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/O9IbWKKh-Ts" height="1" width="1"/&gt;</description><a10:updated>2013-05-03T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Zhong Jin</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NP/C3NP70006B</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NP/C3NP70005D"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NP/C3NP70005D</guid><link>http://feeds.rsc.org/~r/rss/NP/~3/jGNM1uztJTs/C3NP70005D</link><title>Amaryllidaceae and Sceletium alkaloids</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=C3NP70005D" /&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;, 2013, &lt;b&gt;30&lt;/b&gt;,849-868&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NP70005D, Review Article&lt;/div&gt;&lt;div&gt;Zhong Jin&lt;br/&gt;This review summarizes the latest progress on the isolation, biological activity, and chemistry of naturally occurring alkaloids from plants of the Amaryllidaceae family and the structurally closely related &lt;em&gt;Sceletium&lt;/em&gt; species.&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/jGNM1uztJTs" height="1" width="1"/&gt;</description><a10:updated>2013-05-03T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Zhong Jin</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NP/C3NP70005D</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NP/C3NP20116C"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NP/C3NP20116C</guid><link>http://feeds.rsc.org/~r/rss/NP/~3/tDJaVlnK3JY/C3NP20116C</link><title>Marine natural products: synthetic aspects</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=C3NP20116C" /&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;, 2013, &lt;b&gt;30&lt;/b&gt;,783-805&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NP20116C, Review Article&lt;/div&gt;&lt;div&gt;Jonathan C. Morris&lt;br/&gt;An overview of marine natural products synthesis during 2010 is provided.&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/tDJaVlnK3JY" height="1" width="1"/&gt;</description><a10:updated>2013-05-03T00:00:00+01:00</a10:updated><creator xmlns="http://purl.org/dc/elements/1.1/">Jonathan C. Morris</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NP/C3NP20116C</feedburner:origLink></item><item xml:base="http://pubs.rsc.org/en/Content/ArticleLanding/2013/NP/C3NP70016J"><guid isPermaLink="false">http://pubs.rsc.org/en/Content/ArticleLanding/2013/NP/C3NP70016J</guid><link>http://feeds.rsc.org/~r/rss/NP/~3/VElyVFM2AJk/C3NP70016J</link><title>Hirsutellones and beyond: figuring out the biological and synthetic logics toward chemical complexity in fungal PKS-NRPS compounds</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=C3NP70016J" /&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;, 2013, &lt;b&gt;30&lt;/b&gt;,765-782&lt;br/&gt;&lt;b&gt;DOI&lt;/b&gt;: 10.1039/C3NP70016J, Review Article&lt;/div&gt;&lt;div&gt;Xu-Wen Li, Alexandre Ear, Bastien Nay&lt;br/&gt;&lt;strong&gt;Have a game!&lt;/strong&gt; Biosynthetic functionalization can trigger a highly reactive intermediate favourable to cyclization. In this case, the cyclization may be activated by an oxidation of the blue polyketide moiety of the top linear precursor.&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/VElyVFM2AJk" 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/">Xu-Wen Li</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Alexandre Ear</creator><creator xmlns="http://purl.org/dc/elements/1.1/">Bastien Nay</creator><feedburner:origLink>http://pubs.rsc.org/en/Content/ArticleLanding/2013/NP/C3NP70016J</feedburner:origLink></item></channel></rss>
