http://pubs.rsc.org/en/Journals/Journal/NPRSC - Nat. Prod. Rep. latest articlesCopyright (c) The Royal Society of ChemistryFri, 25 May 2012 13:46:14 ZRSC - Nat. Prod. Rep. latest articleshttp://pubs.rsc.org/content/NewImages/rsc_publishing_logo.gifhttp://pubs.rsc.org/en/Journals/Journal/NPhttp://pubs.rsc.org/en/Content/ArticleLanding/2012/NP/C2NP20009Khttp://feeds.rsc.org/~r/rss/NP/~3/kbn9Xz9n27A/C2NP20009K<div><p><img align="center" src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C2NP20009K" /></p></div><div><i><b>Nat. Prod. Rep.</b></i>, 2012, Advance Article<br/><b>DOI</b>: 10.1039/C2NP20009K, Review Article</div><div>Geoffrey E. Ravilious, Joseph M. Jez<br/>This review summarizes the state of our structural knowledge of primary and secondary sulfur assimilatory enzymes from plants.<br/>To cite this article before page numbers are assigned, use the DOI form of citation above.<br/>The content of this RSS Feed (c) The Royal Society of Chemistry</div><img src="http://feeds.feedburner.com/~r/rss/NP/~4/kbn9Xz9n27A" height="1" width="1"/>2012-05-18T00:00:00+01:00Geoffrey E. RaviliousJoseph M. Jezhttp://pubs.rsc.org/en/Content/ArticleLanding/2012/NP/C2NP20009Khttp://pubs.rsc.org/en/Content/ArticleLanding/2012/NP/C2NP20027Ahttp://feeds.rsc.org/~r/rss/NP/~3/kP9qHrbZCUE/C2NP20027A<div><p><img align="center" src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C2NP20027A" /></p></div><div><i><b>Nat. Prod. Rep.</b></i>, 2012, Advance Article<br/><b>DOI</b>: 10.1039/C2NP20027A, Review Article</div><div>Robert A. Hill, Joseph D. Connolly<br/>This review covers the isolation and structure determination of triterpenoids, including squalene derivatives, protostanes, lanostanes, holostanes, cycloartanes, dammaranes, euphanes, tirucallanes, tetranortriterpenoids, quassinoids, lupanes, oleananes, friedelanes, ursanes, hopanes, serratanes and saponins.<br/>To cite this article before page numbers are assigned, use the DOI form of citation above.<br/>The content of this RSS Feed (c) The Royal Society of Chemistry</div><img src="http://feeds.feedburner.com/~r/rss/NP/~4/kP9qHrbZCUE" height="1" width="1"/>2012-05-17T00:00:00+01:00Robert A. HillJoseph D. Connollyhttp://pubs.rsc.org/en/Content/ArticleLanding/2012/NP/C2NP20027Ahttp://pubs.rsc.org/en/Content/ArticleLanding/2012/NP/C2NP20013Ahttp://feeds.rsc.org/~r/rss/NP/~3/FecaM9AQ60M/C2NP20013A<div><p><img align="center" src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C2NP20013A" /></p></div><div><i><b>Nat. Prod. Rep.</b></i>, 2012, Advance Article<br/><b>DOI</b>: 10.1039/C2NP20013A, Highlight</div><div>Jan-Ytzen van der Meer, Anna K. H. Hirsch<br/>The non-mevalonate pathway for the biosynthesis of the isoprenoid precursors is a potential source of targets for the development of innovative antimalarials. This <em>Highlight</em> analyses which isoprenoids are essential for the <em>Plasmodium</em> parasite.<br/>To cite this article before page numbers are assigned, use the DOI form of citation above.<br/>The content of this RSS Feed (c) The Royal Society of Chemistry</div><img src="http://feeds.feedburner.com/~r/rss/NP/~4/FecaM9AQ60M" height="1" width="1"/>2012-05-04T00:00:00+01:00Jan-Ytzen van der MeerAnna K. H. Hirschhttp://pubs.rsc.org/en/Content/ArticleLanding/2012/NP/C2NP20013Ahttp://pubs.rsc.org/en/Content/ArticleLanding/2012/NP/C2NP20021Jhttp://feeds.rsc.org/~r/rss/NP/~3/fnR7pVkN2x8/C2NP20021J<div><p><img align="center" src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C2NP20021J" /></p></div><div><i><b>Nat. Prod. Rep.</b></i>, 2012, <b>29</b>,683-696<br/><b>DOI</b>: 10.1039/C2NP20021J, Review Article</div><div>Jennifer Guerra-Bubb, Rodney Croteau, Robert M. Williams<br/>Taxol has been of interest for decades due to its potent anti-cancer activity. Herein, we discuss progress towards elucidating the biosynthesis of Taxol, as well as bioengineering efforts to produce biosynthetic pathway intermediates.<br/>The content of this RSS Feed (c) The Royal Society of Chemistry</div><img src="http://feeds.feedburner.com/~r/rss/NP/~4/fnR7pVkN2x8" height="1" width="1"/>2012-05-01T00:00:00+01:00Jennifer Guerra-BubbRodney CroteauRobert M. Williamshttp://pubs.rsc.org/en/Content/ArticleLanding/2012/NP/C2NP20021Jhttp://pubs.rsc.org/en/Content/ArticleLanding/2012/NP/C2NP90016Ehttp://feeds.rsc.org/~r/rss/NP/~3/LPmAGsh3J_s/C2NP90016E<div><p><img align="center" src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C2NP90016E" /></p></div><div><i><b>Nat. Prod. Rep.</b></i>, 2012, <b>29</b>,617-621<br/><b>DOI</b>: 10.1039/C2NP90016E, Hot off the Press Article</div><div>Robert A. Hill, Andrew Sutherland<br/>A personal selection of 32 recent papers is presented covering various aspects of current developments in bioorganic chemistry and novel natural products such as neaumycin from a <em>Streptomyces</em> species.<br/>The content of this RSS Feed (c) The Royal Society of Chemistry</div><img src="http://feeds.feedburner.com/~r/rss/NP/~4/LPmAGsh3J_s" height="1" width="1"/>2012-04-30T00:00:00+01:00Robert A. HillAndrew Sutherlandhttp://pubs.rsc.org/en/Content/ArticleLanding/2012/NP/C2NP90016E