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<channel>
	<title>Natural Products Blog</title>
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		<title>Natural Products in OBC – Our latest selection</title>
		<link>http://blogs.rsc.org/np/2013/06/12/natural-products-in-obc-%e2%80%93-our-latest-selection-2/</link>
		<comments>http://blogs.rsc.org/np/2013/06/12/natural-products-in-obc-%e2%80%93-our-latest-selection-2/#comments</comments>
		<pubDate>Wed, 12 Jun 2013 09:26:11 +0000</pubDate>
		<dc:creator>Marie Cote, Deputy Editor</dc:creator>
				<category><![CDATA[Natural Products in OBC]]></category>
		<category><![CDATA[NPR]]></category>
		<category><![CDATA[OBC]]></category>

		<guid isPermaLink="false">http://blogs.rsc.org/np/?p=1220</guid>
		<description><![CDATA[Organic &#38; Biomolecular Chemistry, our sister journal, publishes many articles that cover a variety of natural product chemistry. 
We try to keep you updated here, although your best bet is for you to sign up to OBC’s e-alert (free service), and receive the tables of content directly in your inbox every time an issue is [...]]]></description>
			<content:encoded><![CDATA[<p><a href="http://blogs.rsc.org/np/files/2013/06/GA1.gif"><img class="alignright size-full wp-image-1230" title="GA[1]" src="http://blogs.rsc.org/np/files/2013/06/GA1.gif" alt="" width="148" height="194" /></a><a href="http://pubs.rsc.org/en/journals/journalissues/ob"><em><strong>Organic &amp; Biomolecular Chemistry</strong></em></a><strong>, our sister journal, publishes many articles that cover a variety of natural product chemistry. </strong></p>
<p>We try to keep you updated here, although your best bet is for you to <a href="http://www.rsc.org/Publishing/Journals/forms/V5profile.asp"><strong>sign up</strong> </a>to <em>OBC</em>’s e-alert (free service), and receive the tables of content directly in your inbox every time an issue is published.</p>
<p>Hand-picked for you from the latest issues are:</p>
<p><a href="http://xlink.rsc.org/?doi=10.1039/C3OB40374B"><strong>Concise synthesis of (−)-steviamine and analogues and their glycosidase inhibitory activities</strong></a><br />
Nadechanok Jiangseubchatveera, Marc E. Bouillon, Boonsom Liawruangrath, Saisunee Liawruangrath, Robert J. Nash and Stephen G. Pyne<br />
<strong>DOI</strong>: 10.1039/C3OB40374B, <em>Paper</em></p>
<p><a href="http://xlink.rsc.org/?doi=10.1039/C3OB40480C"><strong>Synthesis of the decalin core of codinaeopsin via an intramolecular Diels–Alder re</strong>action</a><br />
Mani Ramanathan, Chun-Jui Tan, Wen-Jung Chang, Hui-Hsu Gavin Tsai and Duen-Ren Hou<br />
<strong>DOI</strong>: 10.1039/C3OB40480C, <em>Paper</em></p>
<p><a href="http://xlink.rsc.org/?doi=10.1039/C3OB40603B"><strong>Synthesis and antiproliferative activity of selenoindirubins and selenoindirubin-N-glycosides</strong></a><br />
Friedrich Erben, Dennis Kleeblatt, Marcel Sonneck, Martin Hein, Holger Feist, Thomas Fahrenwaldt, Christine Fischer, Abdul Matin, Jamshed Iqbal, Michael Plötz, Jürgen Eberle and Peter Langer<br />
<strong>DOI</strong>: 10.1039/C3OB40603B, <em>Paper</em></p>
<p><a href="http://xlink.rsc.org/?doi=10.1039/C3OB40668G"><strong>Total syntheses of oroidin, hymenidin and clathrodin </strong></a><br />
Sivappa Rasapalli, Venkatreddy Kumbam, Abasaheb N. Dhawane, James A. Golen, Carl J. Lovely and Arnold L. Rheingold<br />
<strong>DOI</strong>: 10.1039/C3OB40668G, <em>Communication</em></p>
<p><a href="http://xlink.rsc.org/?doi=10.1039/C3OB40654G"><strong>Synthesis and biological evaluation of new paclitaxel analogs and discovery of potent antitumor agents</strong></a><br />
Kyriacos C. Nicolaou and Roman A. Valiulin<br />
<strong>DOI</strong>: 10.1039/C3OB40654G, <em>Paper</em></p>
<p><a href="http://xlink.rsc.org/?doi=10.1039/C3OB40363G"><strong>First studies directed towards the diastereoselective synthesis of the BCD tricyclic core of brownin F</strong></a><br />
Fabien Rodier, Jean-Luc Parrain, Gaëlle Chouraqui and Laurent Commeiras<br />
<strong>DOI</strong>: 10.1039/C3OB40363G, <em>Paper</em></p>
<p><a href="http://xlink.rsc.org/?doi=10.1039/C3OB40493E"><strong><strong>Protein engineering of oxidosqualene-lanosterol cyclase into triterpene monocyclase</strong></strong></a><br />
Cheng-Hsiang Chang, Hao-Yu Wen, Wen-Shiang Shie, Ching-Ting Lu, Meng-Erh Li, Yuan-Ting Liu, Wen-Hsuan Li and Tung-Kung Wu<br />
<strong>DOI</strong>: 10.1039/C3OB40493E,<em> Paper</em></p>
<p style="text-align: center">We hope you enjoy this selection! Let us know what you think…</p>
<p style="text-align: center">… and why not <a href="http://mc.manuscriptcentral.com/ob">submit your latest natural product research </a>to <em>OBC</em> today?</p>
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		</item>
		<item>
		<title>Natural Products in OBC – our latest selection</title>
		<link>http://blogs.rsc.org/np/2013/05/15/natural-products-in-obc-%e2%80%93-our-latest-selection/</link>
		<comments>http://blogs.rsc.org/np/2013/05/15/natural-products-in-obc-%e2%80%93-our-latest-selection/#comments</comments>
		<pubDate>Wed, 15 May 2013 09:35:20 +0000</pubDate>
		<dc:creator>Marie Cote, Deputy Editor</dc:creator>
				<category><![CDATA[Natural Products in OBC]]></category>
		<category><![CDATA[NPR]]></category>
		<category><![CDATA[OBC]]></category>

		<guid isPermaLink="false">http://blogs.rsc.org/np/?p=1201</guid>
		<description><![CDATA[Organic &#38; Biomolecular Chemistry, our sister journal, publishes many articles that cover a variety of natural product chemistry. 
We try to keep you updated here, although your best bet is for you to sign up to OBC’s e-alert (free service), and receive the tables of content directly in your inbox every time an issue is [...]]]></description>
			<content:encoded><![CDATA[<p style="text-align: center"><a href="http://pubs.rsc.org/en/journals/journalissues/ob"><em><strong>Organic &amp; Biomolecular Chemistry</strong></em></a><strong>, our sister journal, publishes many articles that cover a variety of natural product chemistry. </strong></p>
<p><a href="http://blogs.rsc.org/np/files/2013/05/GA4.gif"><img class="alignright size-full wp-image-1216" title="GA[4]" src="http://blogs.rsc.org/np/files/2013/05/GA4.gif" alt="" width="148" height="194" /></a>We try to keep you updated here, although your best bet is for you to <a href="http://www.rsc.org/Publishing/Journals/forms/V5profile.asp"><strong>sign up</strong> </a>to <em>OBC</em>’s e-alert (free service), and receive the tables of content directly in your inbox every time an issue is published.</p>
<p>Hand-picked for you from the latest issues are:</p>
<p><a href="http://xlink.rsc.org/?doi=10.1039/C3OB27478K"><strong>Total synthesis of (+)-pentamethylsalvianolic acid C</strong></a><br />
Benjamin L. Alford and Helmut M. Hügel<br />
<em>Org. Biomol. Chem.</em>, 2013,11, 2724-2727<br />
<strong>DOI</strong>: 10.1039/C3OB27478K, Paper</p>
<p><a href="http://xlink.rsc.org/?doi=10.1039/C3OB40180D"><strong>Concise total syntheses of (±)-noruleine and (±)-uleine</strong></a><br />
Süleyman Patir and Erkan Ertürk<br />
<em>Org. Biomol. Chem.</em>, 2013,11, 2804-2810<br />
<strong>DOI</strong>: 10.1039/C3OB40180D, Paper</p>
<p><a href="http://xlink.rsc.org/?doi=10.1039/C3OB40208H"><strong>A concise approach to the spiroiminal fragment of marin</strong>eosins</a><br />
Guang Li, Xun Zhang, Qi Li, Pengju Feng and Yian Shi<br />
<em>Org. Biomol. Chem.</em>, 2013,11, 2936-2938<br />
<strong>DOI</strong>: 10.1039/C3OB40208H, Communication</p>
<p><a href="http://xlink.rsc.org/?doi=10.1039/C3OB27390C"><strong>Highly stereoselective directed reactions and an efficient synthesis of azafuranoses from a chiral aziridine</strong></a><br />
Hogyu Lee, Jun Hee Kim, Won Koo Lee, Jaeheung Cho, Wonwoo Nam, Jaedeok Lee and Hyun-Joon Ha<br />
<em>Org. Biomol. Chem.</em>, 2013,11, 3629-3634<br />
<strong>DOI</strong>: 10.1039/C3OB27390C, Paper</p>
<p style="text-align: center">We hope you enjoy this selection! Let us know what you think…</p>
<p style="text-align: center">… and why not <a href="http://mc.manuscriptcentral.com/ob">submit your latest natural product research </a>to <em>OBC</em> today?</p>
<div class="lightsocial_container"><a class="lightsocial_a" href="http://digg.com/submit?url=http%3A%2F%2Fblogs.rsc.org%2Fnp%2F2013%2F05%2F15%2Fnatural-products-in-obc-%25e2%2580%2593-our-latest-selection%2F&amp;title=Natural+Products+in+OBC+%E2%80%93+our+latest+selection" ><img class="lightsocial_img" src="http://blogs.rsc.org/np/wp-content/plugins/light-social/digg.png" alt="Digg This" title="Digg This" /></a>&nbsp;&nbsp;<a class="lightsocial_a" href="http://www.reddit.com/submit?url=http%3A%2F%2Fblogs.rsc.org%2Fnp%2F2013%2F05%2F15%2Fnatural-products-in-obc-%25e2%2580%2593-our-latest-selection%2F&amp;title=Natural+Products+in+OBC+%E2%80%93+our+latest+selection" ><img class="lightsocial_img" src="http://blogs.rsc.org/np/wp-content/plugins/light-social/reddit.png" alt="Reddit This" title="Reddit This" /></a>&nbsp;&nbsp;<a class="lightsocial_a" href="http://www.stumbleupon.com/submit?url=http%3A%2F%2Fblogs.rsc.org%2Fnp%2F2013%2F05%2F15%2Fnatural-products-in-obc-%25e2%2580%2593-our-latest-selection%2F&amp;title=Natural+Products+in+OBC+%E2%80%93+our+latest+selection" ><img class="lightsocial_img" src="http://blogs.rsc.org/np/wp-content/plugins/light-social/stumbleupon.png" alt="Stumble Now!" title="Stumble Now!" /></a>&nbsp;&nbsp;<a class="lightsocial_a" href="http://www.facebook.com/sharer.php?t=Natural+Products+in+OBC+%E2%80%93+our+latest+selection&amp;u=http%3A%2F%2Fblogs.rsc.org%2Fnp%2F2013%2F05%2F15%2Fnatural-products-in-obc-%25e2%2580%2593-our-latest-selection%2F" ><img class="lightsocial_img" src="http://blogs.rsc.org/np/wp-content/plugins/light-social/facebook.png" alt="Share on Facebook" title="Share on Facebook" /></a>&nbsp;&nbsp;<a class="lightsocial_a" href="http://delicious.com/save?title=Natural+Products+in+OBC+%E2%80%93+our+latest+selection&amp;url=http%3A%2F%2Fblogs.rsc.org%2Fnp%2F2013%2F05%2F15%2Fnatural-products-in-obc-%25e2%2580%2593-our-latest-selection%2F" ><img class="lightsocial_img" src="http://blogs.rsc.org/np/wp-content/plugins/light-social/delicious.png" alt="Bookmark this on Delicious" title="Bookmark this on Delicious" /></a>&nbsp;&nbsp;<a class="lightsocial_a" href="http://www.linkedin.com/shareArticle?mini=true&amp;url=http%3A%2F%2Fblogs.rsc.org%2Fnp%2F2013%2F05%2F15%2Fnatural-products-in-obc-%25e2%2580%2593-our-latest-selection%2F&amp;title=Natural+Products+in+OBC+%E2%80%93+our+latest+selection&amp;summary=&amp;source=" ><img class="lightsocial_img" src="http://blogs.rsc.org/np/wp-content/plugins/light-social/linkedin.png" alt="Share on LinkedIn" title="Share on LinkedIn" /></a>&nbsp;&nbsp;<a class="lightsocial_a" href="http://www.technorati.com/faves?add=http%3A%2F%2Fblogs.rsc.org%2Fnp%2F2013%2F05%2F15%2Fnatural-products-in-obc-%25e2%2580%2593-our-latest-selection%2F" ><img class="lightsocial_img" src="http://blogs.rsc.org/np/wp-content/plugins/light-social/technorati.png" alt="Bookmark this on Technorati" title="Bookmark this on Technorati" /></a>&nbsp;&nbsp;<a class="lightsocial_a" href="http://twitter.com/home?status=Reading+http%3A%2F%2Fblogs.rsc.org%2Fnp%2F2013%2F05%2F15%2Fnatural-products-in-obc-%25e2%2580%2593-our-latest-selection%2F" ><img class="lightsocial_img" src="http://blogs.rsc.org/np/wp-content/plugins/light-social/twitter.png" alt="Post on Twitter" title="Post on Twitter" /></a>&nbsp;&nbsp;<a class="lightsocial_a" href="http://www.google.com/buzz/post?url=http%3A%2F%2Fblogs.rsc.org%2Fnp%2F2013%2F05%2F15%2Fnatural-products-in-obc-%25e2%2580%2593-our-latest-selection%2F" ><img class="lightsocial_img" src="http://blogs.rsc.org/np/wp-content/plugins/light-social/google_buzz.png" alt="Google Buzz (aka. Google Reader)" title="Google Buzz (aka. Google Reader)" /></a>&nbsp;&nbsp;</div>]]></content:encoded>
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		<title>NPR Top 10 most accessed articles published in 2012 (Volume 29)</title>
		<link>http://blogs.rsc.org/np/2013/04/15/npr-top-10-most-accessed-articles-published-in-2012-volume-29/</link>
		<comments>http://blogs.rsc.org/np/2013/04/15/npr-top-10-most-accessed-articles-published-in-2012-volume-29/#comments</comments>
		<pubDate>Mon, 15 Apr 2013 09:23:06 +0000</pubDate>
		<dc:creator>Aliya Anwar</dc:creator>
				<category><![CDATA[Top 10]]></category>
		<category><![CDATA[NPR]]></category>

		<guid isPermaLink="false">http://blogs.rsc.org/np/?p=1205</guid>
		<description><![CDATA[Curious about which articles published in 2012 gathered most readership? Here are the Top 10 works your colleagues have been accessing in Natural Product Reports:
Marine natural products
John W. Blunt, Brent R. Copp, Robert A. Keyzers, Murray H. G. Munro and Michèle R. Prinsep
Nat. Prod. Rep., 2012, 29, 144-222
DOI: 10.1039/C2NP00090C
Recent discovery of plant-derived anti-diabetic natural products
Hsin-Yi Hung, [...]]]></description>
			<content:encoded><![CDATA[<p><a href="http://blogs.rsc.org/np/files/2013/04/GACA4LNOFZ.gif"><img class="alignright size-full wp-image-1210" title="GACA4LNOFZ" src="http://blogs.rsc.org/np/files/2013/04/GACA4LNOFZ.gif" alt="" width="148" height="194" /></a>Curious about which articles published in 2012 gathered most readership? Here are the Top 10 works your colleagues have been accessing in <em><a href="http://pubs.rsc.org/en/journals/journalissues/np"><strong>Natural Product Reports</strong></a></em>:</p>
<p><strong><a href="http://xlink.rsc.org/?doi=10.1039/C2NP00090C">Marine natural products<br />
</a></strong>John W. Blunt, Brent R. Copp, Robert A. Keyzers, Murray H. G. Munro and Michèle R. Prinsep<br />
<strong><em>Nat. Prod. Rep.,</em></strong> 2012, <strong>29</strong>, 144-222<br />
<strong>DOI</strong>: 10.1039/C2NP00090C</p>
<p><strong><a href="http://xlink.rsc.org/?doi=10.1039/C2NP00074A">Recent discovery of plant-derived anti-diabetic natural products<br />
</a></strong>Hsin-Yi Hung, Keduo Qian, Susan L. Morris-Natschke, Chau-Shin Hsu and Kuo-Hsiung Lee<br />
<strong><em>Nat. Prod. Rep.,</em></strong> 2012, <strong>29</strong>, 580-606<br />
<strong>DOI</strong>: 10.1039/C2NP00074A</p>
<p><strong><a href="http://xlink.rsc.org/?doi=10.1039/C2NP00084A">Advances in <em>Aspergillus</em> secondary metabolite research in the post-genomic era<br />
</a></strong>James F. Sanchez, Amber D. Somoza, Nancy P. Keller and Clay C. C. Wang<br />
<strong><em>Nat. Prod. Rep.,</em></strong> 2012, <strong>29</strong>, 351-371<br />
<strong>DOI</strong>: 10.1039/C2NP00084A</p>
<p><strong><a href="http://xlink.rsc.org/?doi=10.1039/C1NP00053E">Influenza neuraminidase: A druggable target for natural products<br />
</a></strong>Ulrike Grienke, Michaela Schmidtke, Susanne von Grafenstein, Johannes Kirchmair, Klaus R. Liedl and Judith M. Rollinger<br />
<strong><em>Nat. Prod. Rep.,</em></strong> 2012, <strong>29</strong>, 11-36<br />
<strong>DOI</strong>: 10.1039/C1NP00053E</p>
<p><strong><a href="http://xlink.rsc.org/?doi=10.1039/C2NP00097K">Natural products as kinase inhibitors<br />
</a></strong>Jing Liu, Yi Hu, David L. Waller, Junfeng Wang and Qingsong Liu<br />
<strong><em>Nat. Prod. Rep.,</em></strong> 2012, <strong>29</strong>, 392-403<br />
<strong>DOI</strong>: 10.1039/C2NP00097K</p>
<p><strong><a href="http://xlink.rsc.org/?doi=10.1039/C2NP00075J">The chemical ecology of cyanobacteria<br />
</a></strong>Pedro N. Leão, Niclas Engene, Agostinho Antunes, William H. Gerwick and Vitor Vasconcelos<br />
<strong><em>Nat. Prod. Rep.,</em></strong> 2012, <strong>29</strong>, 372-391<br />
<strong>DOI</strong>: 10.1039/C2NP00075J</p>
<p><strong><a href="http://xlink.rsc.org/?doi=10.1039/C2NP20012K">Electrophilic natural products and their biological targets<br />
</a></strong>Malte Gersch, Johannes Kreuzer and Stephan A. Sieber<br />
<strong><em>Nat. Prod. Rep.,</em></strong> 2012, <strong>29</strong>, 659-682<br />
<strong>DOI</strong>: 10.1039/C2NP20012K</p>
<p><strong><a href="http://xlink.rsc.org/?doi=10.1039/C2NP00073C">The taxonomy, biology and chemistry of the fungal Pestalotiopsis genus<br />
</a></strong>Xiao-Long Yang, Jing-Ze Zhang and Du-Qiang Luo<br />
<strong><em>Nat. Prod. Rep.,</em></strong> 2012, <strong>29</strong>, 622-641<br />
<strong>DOI</strong>: 10.1039/C2NP00073C</p>
<p><strong><a href="http://xlink.rsc.org/?doi=10.1039/C1NP00072A">Aminobenzoates as building blocks for natural product assembly lines<br />
</a></strong>Christopher T. Walsh, Stuart W. Haynes and Brian D. Ames<br />
<strong><em>Nat. Prod. Rep.,</em></strong> 2012, <strong>29</strong>, 37-59<br />
<strong>DOI</strong>: 10.1039/C1NP00072A</p>
<p><strong><a href="http://xlink.rsc.org/?doi=10.1039/C2NP20034A">Strained cyclophane natural products: Macrocyclization at its limits<br />
</a></strong>Tanja Gulder and Phil S. Baran<br />
<strong><em>Nat. Prod. Rep.,</em></strong> 2012, <strong>29</strong>, 899-934<br />
<strong>DOI</strong>: 10.1039/C2NP20034A</p>
<p style="text-align: center"><strong>Interested in submitting your own work to <em>NPR</em>? </strong><a href="http://mc.manuscriptcentral.com/np" target="_blank"><strong>Submit online</strong></a><strong> today, or </strong><a href="mailto:npr-rsc@rsc.org" target="_blank"><strong>email us</strong></a><strong> with your suggestions!</strong></p>
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		<title>Polycyclic xanthones, cryptic secondary metabolome, steroidal glycosides: take your pick!</title>
		<link>http://blogs.rsc.org/np/2013/02/19/polycyclic-xanthones-cryptic-secondary-metabolome-steroidal-glycosides-take-your-pick/</link>
		<comments>http://blogs.rsc.org/np/2013/02/19/polycyclic-xanthones-cryptic-secondary-metabolome-steroidal-glycosides-take-your-pick/#comments</comments>
		<pubDate>Tue, 19 Feb 2013 15:42:43 +0000</pubDate>
		<dc:creator>Marie Cote, Deputy Editor</dc:creator>
				<category><![CDATA[News]]></category>
		<category><![CDATA[MedChemComm]]></category>
		<category><![CDATA[NPR]]></category>
		<category><![CDATA[OBC]]></category>

		<guid isPermaLink="false">http://blogs.rsc.org/np/?p=1180</guid>
		<description><![CDATA[Welcome to NPR Issue 3, 2013

I do not know about you, but I find these circular genome data visualization plots make amazing covers. The one featured on this month&#8217;s issue illustrates the exciting review article by Christian Hertweck et al., presenting a genomic approach to the cryptic secondary metabolome of the anaerobic word.
Read this article for [...]]]></description>
			<content:encoded><![CDATA[<p style="text-align: center"><strong>Welcome to <em>NPR</em> </strong><a href="http://pubs.rsc.org/en/journals/journalissues/np#!issueid=np030003&amp;type=current&amp;issnprint=0265-0568"><strong>Issue 3, 2013</strong></a></p>
<p><a href="http://blogs.rsc.org/np/files/2013/02/GA8.gif"><img class="alignright size-full wp-image-1181" title="GA[8]" src="http://blogs.rsc.org/np/files/2013/02/GA8.gif" alt="" width="148" height="194" /></a></p>
<p>I do not know about you, but I find these circular genome data visualization plots make amazing covers. The one featured on this month&#8217;s issue illustrates the exciting review article by <strong>Christian Hertweck</strong> <em>et al.</em>, presenting a <a href="http://pubs.rsc.org/en/content/articlelanding/2013/np/c2np20103h">genomic approach to the cryptic secondary metabolome of the anaerobic word</a>.</p>
<p>Read this article <strong>for Free</strong> for the next 6 weeks &#8211; and let us know what you think by posting a comment below!</p>
<p>You will remember that Professor Hertweck was the winner of the <a href="http://blogs.rsc.org/np/2011/01/26/christian-hertweck-wins-2011-npr-lecture-award/">2011 <em>NPR</em> Lecture Award</a>, and so that you may read more about his work at the forefront of natural products research, we&#8217;ve collated two of his previous <em>NPR</em> review articles below:</p>
<p><a href="http://pubs.rsc.org/en/Content/ArticleLanding/2010/NP/B903913A">The chemistry and biology of cytochalasans </a><br />
Kirstin Scherlach, Daniela Boettger, Nicole Remme and Christian Hertweck<br />
<a href="http://pubs.rsc.org/en/Journals/Journal/NP"><strong><em>Nat. Prod. Rep.</em></strong></a>, 2010, <strong>27</strong>, 869-886 </p>
<p><a href="http://pubs.rsc.org/en/Content/ArticleLanding/2007/NP/B507395M">Type II polyketide synthases: gaining a deeper insight into enzymatic teamwork </a><br />
Christian Hertweck, Andriy Luzhetskyy, Yuri Rebets and Andreas Bechthold<br />
<a href="http://pubs.rsc.org/en/Journals/Journal/NP"><strong><em>Nat. Prod. Rep.</em></strong></a>, 2007, <strong>24</strong>, 162-190 </p>
<p><span style="font-family: MyriadPro-Regular;font-size: xx-small"><span style="font-family: MyriadPro-Regular;font-size: xx-small"><a href="http://blogs.rsc.org/np/files/2013/02/GA6.gif"><img class="alignright size-full wp-image-1182" title="GA[6]" src="http://blogs.rsc.org/np/files/2013/02/GA6.gif" alt="" width="324" height="106" /></a></span></span></p>
<p>This issue&#8217;s <a href="http://pubs.rsc.org/en/content/articlelanding/2013/np/c3np20122h">Highlight article </a>is by <strong>John A. Porco Jr.</strong> <em>et al.</em> and summarizes key advancements in the construction of polycyclic xanthones, which have recently attracted significant attention due to their potential as antitumour agents.</p>
<p>Then, Victoria L. Challinor and <strong>James J. De Voss</strong> review the structure elucidation, bioactivities, biosynthesis, and distribution in the plant kingdom of <a href="http://pubs.rsc.org/en/content/articlelanding/2013/np/c3np20105h">open-chain steroidal glycosides</a>, which represent a numerous, structurally diverse class of plant saponins.</p>
<p>Finally<strong> Yonghong Liu</strong> <em>et al.</em> provide an up-to-date account of <a href="http://pubs.rsc.org/en/content/articlelanding/2013/np/c3np20089b">sesterterpenoids</a>, which structural conciseness and diverse bioactivity have made them attractive targets to the synthetic chemist, with biomedical purposes. </p>
<p style="text-align: center">Short and sweet, a selection we hope you will like!</p>
<div class="lightsocial_container"><a class="lightsocial_a" href="http://digg.com/submit?url=http%3A%2F%2Fblogs.rsc.org%2Fnp%2F2013%2F02%2F19%2Fpolycyclic-xanthones-cryptic-secondary-metabolome-steroidal-glycosides-take-your-pick%2F&amp;title=Polycyclic+xanthones%2C+cryptic+secondary+metabolome%2C+steroidal+glycosides%3A+take+your+pick%21" ><img class="lightsocial_img" src="http://blogs.rsc.org/np/wp-content/plugins/light-social/digg.png" alt="Digg This" title="Digg This" /></a>&nbsp;&nbsp;<a class="lightsocial_a" href="http://www.reddit.com/submit?url=http%3A%2F%2Fblogs.rsc.org%2Fnp%2F2013%2F02%2F19%2Fpolycyclic-xanthones-cryptic-secondary-metabolome-steroidal-glycosides-take-your-pick%2F&amp;title=Polycyclic+xanthones%2C+cryptic+secondary+metabolome%2C+steroidal+glycosides%3A+take+your+pick%21" ><img class="lightsocial_img" src="http://blogs.rsc.org/np/wp-content/plugins/light-social/reddit.png" alt="Reddit This" title="Reddit This" /></a>&nbsp;&nbsp;<a class="lightsocial_a" href="http://www.stumbleupon.com/submit?url=http%3A%2F%2Fblogs.rsc.org%2Fnp%2F2013%2F02%2F19%2Fpolycyclic-xanthones-cryptic-secondary-metabolome-steroidal-glycosides-take-your-pick%2F&amp;title=Polycyclic+xanthones%2C+cryptic+secondary+metabolome%2C+steroidal+glycosides%3A+take+your+pick%21" ><img class="lightsocial_img" src="http://blogs.rsc.org/np/wp-content/plugins/light-social/stumbleupon.png" alt="Stumble Now!" title="Stumble Now!" /></a>&nbsp;&nbsp;<a class="lightsocial_a" href="http://www.facebook.com/sharer.php?t=Polycyclic+xanthones%2C+cryptic+secondary+metabolome%2C+steroidal+glycosides%3A+take+your+pick%21&amp;u=http%3A%2F%2Fblogs.rsc.org%2Fnp%2F2013%2F02%2F19%2Fpolycyclic-xanthones-cryptic-secondary-metabolome-steroidal-glycosides-take-your-pick%2F" ><img class="lightsocial_img" src="http://blogs.rsc.org/np/wp-content/plugins/light-social/facebook.png" alt="Share on Facebook" title="Share on Facebook" /></a>&nbsp;&nbsp;<a class="lightsocial_a" href="http://delicious.com/save?title=Polycyclic+xanthones%2C+cryptic+secondary+metabolome%2C+steroidal+glycosides%3A+take+your+pick%21&amp;url=http%3A%2F%2Fblogs.rsc.org%2Fnp%2F2013%2F02%2F19%2Fpolycyclic-xanthones-cryptic-secondary-metabolome-steroidal-glycosides-take-your-pick%2F" ><img class="lightsocial_img" src="http://blogs.rsc.org/np/wp-content/plugins/light-social/delicious.png" alt="Bookmark this on Delicious" title="Bookmark this on Delicious" /></a>&nbsp;&nbsp;<a class="lightsocial_a" href="http://www.linkedin.com/shareArticle?mini=true&amp;url=http%3A%2F%2Fblogs.rsc.org%2Fnp%2F2013%2F02%2F19%2Fpolycyclic-xanthones-cryptic-secondary-metabolome-steroidal-glycosides-take-your-pick%2F&amp;title=Polycyclic+xanthones%2C+cryptic+secondary+metabolome%2C+steroidal+glycosides%3A+take+your+pick%21&amp;summary=&amp;source=" ><img class="lightsocial_img" src="http://blogs.rsc.org/np/wp-content/plugins/light-social/linkedin.png" alt="Share on LinkedIn" title="Share on LinkedIn" /></a>&nbsp;&nbsp;<a class="lightsocial_a" href="http://www.technorati.com/faves?add=http%3A%2F%2Fblogs.rsc.org%2Fnp%2F2013%2F02%2F19%2Fpolycyclic-xanthones-cryptic-secondary-metabolome-steroidal-glycosides-take-your-pick%2F" ><img class="lightsocial_img" src="http://blogs.rsc.org/np/wp-content/plugins/light-social/technorati.png" alt="Bookmark this on Technorati" title="Bookmark this on Technorati" /></a>&nbsp;&nbsp;<a class="lightsocial_a" href="http://twitter.com/home?status=Reading+http%3A%2F%2Fblogs.rsc.org%2Fnp%2F2013%2F02%2F19%2Fpolycyclic-xanthones-cryptic-secondary-metabolome-steroidal-glycosides-take-your-pick%2F" ><img class="lightsocial_img" src="http://blogs.rsc.org/np/wp-content/plugins/light-social/twitter.png" alt="Post on Twitter" title="Post on Twitter" /></a>&nbsp;&nbsp;<a class="lightsocial_a" href="http://www.google.com/buzz/post?url=http%3A%2F%2Fblogs.rsc.org%2Fnp%2F2013%2F02%2F19%2Fpolycyclic-xanthones-cryptic-secondary-metabolome-steroidal-glycosides-take-your-pick%2F" ><img class="lightsocial_img" src="http://blogs.rsc.org/np/wp-content/plugins/light-social/google_buzz.png" alt="Google Buzz (aka. Google Reader)" title="Google Buzz (aka. Google Reader)" /></a>&nbsp;&nbsp;</div>]]></content:encoded>
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		</item>
		<item>
		<title>Natural Products in OBC &#8211; our latest selection</title>
		<link>http://blogs.rsc.org/np/2013/02/06/natural-products-in-obc-our-latest-selection-3/</link>
		<comments>http://blogs.rsc.org/np/2013/02/06/natural-products-in-obc-our-latest-selection-3/#comments</comments>
		<pubDate>Wed, 06 Feb 2013 10:28:20 +0000</pubDate>
		<dc:creator>Marie Cote, Deputy Editor</dc:creator>
				<category><![CDATA[Natural Products in OBC]]></category>
		<category><![CDATA[NPR]]></category>
		<category><![CDATA[OBC]]></category>

		<guid isPermaLink="false">http://blogs.rsc.org/np/?p=1137</guid>
		<description><![CDATA[Organic &#38; Biomolecular Chemistry, our sister journal, publishes many articles that cover a variety of natural product chemistry. 
We try to keep you updated here, although your best bet is for you to sign up to OBC’s e-alert (free service), and receive the tables of content directly in your inbox every time an issue is [...]]]></description>
			<content:encoded><![CDATA[<p><strong><a href="http://blogs.rsc.org/np/files/2013/02/OBC.gif"><img class="alignright size-full wp-image-1175" title="OBC" src="http://blogs.rsc.org/np/files/2013/02/OBC.gif" alt="" width="148" height="194" /></a><a href="http://pubs.rsc.org/en/journals/journalissues/ob">Organic &amp; Biomolecular Chemistry</a><strong>, our sister journal, publishes many articles that cover a variety of natural product chemistry. </strong></strong></p>
<p>We try to keep you updated here, although your best bet is for you to <a href="http://www.rsc.org/Publishing/Journals/forms/V5profile.asp"><strong>sign up</strong> </a>to <em>OBC</em>’s e-alert (free service), and receive the tables of content directly in your inbox every time an issue is published.</p>
<p>Hand-picked for you from the latest issues are:</p>
<p><a href="http://xlink.rsc.org/?doi=10.1039/C2OB26931G"><strong>Watsonianone A–C, anti-plasmodial β-triketones from the Australian tree, Corymbia watsoniana</strong></a><br />
Anthony R. Carroll, Vicky M. Avery, Sandra Duffy, Paul I. Forster and Gordon P. Guymer<br />
<em>Org. Biomol. Chem.</em>, 2013,11, 453-458<br />
DOI: 10.1039/C2OB26931G, Paper</p>
<p><a href="http://xlink.rsc.org/?doi=10.1039/C2OB26737C"><strong>A mechanistic study on the Hooker oxidation: synthesis of novel indane carboxylic acid derivatives from lapachol</strong></a><br />
Kenneth O. Eyong, Manohar Puppala, Ponminor Senthil Kumar, Marc Lamshöft, Gabriel N. Folefoc, Michael Spiteller and Sundarababu Baskaran<br />
<em>Org. Biomol. Chem.</em>, 2013,11, 459-468<br />
DOI: 10.1039/C2OB26737C, Paper</p>
<p><a href="http://xlink.rsc.org/?doi=10.1039/C2OB25866H"><strong>Synthesis of N,N′-diglycosylated isoindigos</strong></a><br />
Dennis Kleeblatt, Baraa Siyo, Martin Hein, Viktor O. Iaroshenko, Jamshed Iqbal, Alexander Villinger and Peter Langer<br />
<em>Org. Biomol. Chem.</em>, 2013,11, 886-895<br />
DOI: 10.1039/C2OB25866H, Communication</p>
<p><a href="http://xlink.rsc.org/?doi=10.1039/C2OB26329G"><strong>First total synthesis of Debilisone C</strong></a><br />
Bishwajit Saikia, Thongam Joymati Devi and Nabin C. Barua<br />
<em>Org. Biomol. Chem.</em>, 2013,11, 905-913<br />
DOI: 10.1039/C2OB26329G, Paper</p>
<p><a href="http://xlink.rsc.org/?doi=10.1039/C3OB27238A"><strong>Synthesis and biological studies of neopetrosiamides as inhibitors of cancer cell invasion</strong></a><br />
Kaitlyn M. Towle, Jennifer L. Chaytor, Hongqiang Liu, Pamela Austin, Michel Roberge, Calvin D. Roskelley and John C. Vederas<br />
<em>Org. Biomol. Chem.</em>, 2013, Advance Article<br />
DOI: 10.1039/C3OB27238A, Paper</p>
<p><a href="http://xlink.rsc.org/?doi=10.1039/C3OB26909D"><strong>Stereoselective syntheses of racemic quercitols and bromoquercitols starting from cyclohexa-1,4-diene: gala-, epi-, muco-, and neo-quercitol </strong></a>Gökay Aydın, Tahir Savran, Fatih Aktaş, Arif Baran and Metin Balci<br />
<em>Org. Biomol. Chem.</em>, 2013, Advance Article<br />
DOI: 10.1039/C3OB26909D, Paper</p>
<p style="text-align: center">We hope you enjoy this selection! Let us know what you think…</p>
<p style="text-align: center">… and why not <a href="http://mc.manuscriptcentral.com/ob">submit your latest natural product research </a>to <em>OBC</em> today?</p>
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		<title>Thiopeptide antibiotics, alpha-haloaldehydes, marine natural products and anticancer steroids &#8211; Your NPR issue 2</title>
		<link>http://blogs.rsc.org/np/2013/01/21/thiopeptide-antibiotics-alpha-haloaldehydes-marine-natural-products-and-anticancer-steroids-your-npr-issue-2/</link>
		<comments>http://blogs.rsc.org/np/2013/01/21/thiopeptide-antibiotics-alpha-haloaldehydes-marine-natural-products-and-anticancer-steroids-your-npr-issue-2/#comments</comments>
		<pubDate>Mon, 21 Jan 2013 11:37:53 +0000</pubDate>
		<dc:creator>Marie Cote, Deputy Editor</dc:creator>
				<category><![CDATA[Uncategorized]]></category>
		<category><![CDATA[MedChemComm]]></category>
		<category><![CDATA[NPR]]></category>
		<category><![CDATA[OBC]]></category>

		<guid isPermaLink="false">http://blogs.rsc.org/np/?p=1163</guid>
		<description><![CDATA[

Welcome to NPR Issue 2, 2013 
Issue 2s, home to the much awaited Marine Natural Products review by John Blunt et al., and much more.
Featuring on the front cover is the work of Jorge A. R. Salvador, M. Luisa Sá e Melo and colleagues at University of Coimbra and Universidade da Beira Interior (Portugal), illustrating [...]]]></description>
			<content:encoded><![CDATA[<p><a href="http://blogs.rsc.org/np/files/2013/01/GA9.gif"><img class="alignleft size-full wp-image-1162" title="GA[9]" src="http://blogs.rsc.org/np/files/2013/01/GA9.gif" alt="" width="148" height="194" /></a><br />
<code></code></p>
<p style="text-align: center"><a href="http://pubs.rsc.org/en/journals/journalissues/np#!issueid=np030002&amp;type=current&amp;issnprint=0265-0568"><strong>Welcome to <em>NPR</em> Issue 2, 2013 </strong></a></p>
<p>Issue 2s, home to the much awaited <a href="http://xlink.rsc.org/?doi=10.1039/C2NP20112G">Marine Natural Products </a>review by John Blunt <em>et al.</em>, and much more.</p>
<p>Featuring on the front cover is the work of Jorge A. R. Salvador, M. Luisa Sá e Melo and colleagues at University of Coimbra and Universidade da Beira Interior (Portugal), illustrating their review detailing the anticancer activity of steroids.<br />
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<p><strong>In this issue:</strong></p>
<p><a href="http://xlink.rsc.org/?doi=10.1039/C2NP90051C"><strong>Hot off the press </strong></a><br />
Robert A. Hill and Andrew Sutherland<br />
<strong>DOI</strong>: 10.1039/C2NP90051C</p>
<p><span style="color: #616161">A personal selection of 33 recent papers is presented covering various aspects of current developments in bioorganic chemistry and novel natural products such as breitfussin A from the Arctic hydrozoan Thuiaria breitfussi.</span></p>
<p><a href="http://xlink.rsc.org/?doi=10.1039/C2NP20107K"><strong>Biosynthesis of thiopeptide antibiotics and their pathway engineering</strong></a><br />
Qi Zhang and Wen Liu<br />
<strong>DOI</strong>: 10.1039/C2NP20107K</p>
<p><span style="color: #616161">A Highlight including advances during 2009–2012 in understanding the generality and specificity of thiopeptide biosynthesis, and on this basis, in expanding the structural diversity by pathway engineering.</span></p>
<p><span style="color: #616161"> </span><a href="http://xlink.rsc.org/?doi=10.1039/C2NP20108A"><strong>α-Haloaldehydes: versatile building blocks for natural product synthesis</strong></a><br />
Robert Britton and Baldip Kang<br />
DOI: 10.1039/C2NP20108A</p>
<p><span style="color: #616161">This Highlight summarizes the organocatalytic processes available for the enantioselective preparation of α-haloaldehydes and their stereoselective conversion into natural products.</span></p>
<p><a href="http://xlink.rsc.org/?doi=10.1039/C2NP20112G"><strong>Marine natural products </strong></a><br />
John W. Blunt, Brent R. Copp, Robert A. Keyzers, Murray H. G. Munro and Michèle R. Prinsep<br />
<strong>DOI</strong>: 10.1039/C2NP20112G</p>
<p><span style="color: #616161">The much awaited Marine Natural Products review article! Included is an example of the development of genome mining for the discovery of new compounds from marine microbes leading to the finding of salinosporamide K from <em>Salinispora pacifica</em>.</span></p>
<p>Missed the previous ones? Catch up with the past 5 years of this series:<br />
<a href="http://xlink.rsc.org/?doi=10.1039/C2NP00090C">Marine Natural Products &#8211; 2012</a><br />
<a href="http://xlink.rsc.org/?doi=10.1039/C005001F">Marine Natural Products &#8211; 2011</a><br />
<a href="http://xlink.rsc.org/?doi=10.1039/B906091J">Marine Natural Products &#8211; 2010</a><br />
<a href="http://xlink.rsc.org/?doi=10.1039/B805113P">Marine Natural Products &#8211; 2009</a><br />
<a href="http://xlink.rsc.org/?doi=10.1039/B701534H">Marine Natural Products &#8211; 2008</a></p>
<p><a href="http://xlink.rsc.org/?doi=10.1039/C2NP20082A"><strong>Anticancer steroids: linking natural and semi-synthetic compounds</strong></a><br />
Jorge A. R. Salvador, João F. S. Carvalho, Marco A. C. Neves, Samuel M. Silvestre, Alcino J. Leitão, M. Manuel C. Silva and M. Luisa Sá e Melo<br />
<strong>DOI</strong>: 10.1039/C2NP20082A</p>
<p><span style="color: #616161">Steroids, a widespread class of natural compounds, have shown great therapeutic value for a broad array of pathologies. This overview is focused on their anticancer activity, which is very representative of a rich structural diversity and ability to interact with various biological targets and pathways.</span></p>
<p><strong>Want to see your work in <em>NPR</em>?</strong></p>
<p>Reviews, Highlights and Viewpoints in <em>NPR</em> are generally solicited by members of the editorial board; however we are happy to consider submission enquiries from authors. If you are interested in writing an article for <em>NPR</em> please contact the editorial office with a <a href="http://www.rsc.org/publishing/journals/np/about.asp">brief synopsis</a>.</p>
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		<title>Welcome to Professor Daniel Romo who joins the NPR Editorial Board</title>
		<link>http://blogs.rsc.org/np/2013/01/07/welcome-to-professor-daniel-romo-who-joins-the-npr-editorial-board/</link>
		<comments>http://blogs.rsc.org/np/2013/01/07/welcome-to-professor-daniel-romo-who-joins-the-npr-editorial-board/#comments</comments>
		<pubDate>Mon, 07 Jan 2013 10:39:20 +0000</pubDate>
		<dc:creator>Marie Cote, Deputy Editor</dc:creator>
				<category><![CDATA[Board News]]></category>
		<category><![CDATA[NPR]]></category>

		<guid isPermaLink="false">http://blogs.rsc.org/np/?p=1151</guid>
		<description><![CDATA[We are delighted to announce the appointment of Professor Daniel Romo to the Editorial Board of Natural Products Reports, as of January 2013. 
Daniel Romo received his B.A. in chemistry/biology from Texas A&#38;M and a PhD in Chemistry from Colorado State University as a NSF Minority Graduate Fellow under the tutelage of the late Prof. Albert [...]]]></description>
			<content:encoded><![CDATA[<p>We are delighted to announce the appointment of <a href="http://www.chem.tamu.edu/rgroup/romo/index.html"><strong>Professor Daniel Romo</strong> </a>to the Editorial Board of <em>Natural Products Reports</em>, as of January 2013. </p>
<p><a href="http://blogs.rsc.org/np/files/2013/01/th6.jpg"></a><a href="http://blogs.rsc.org/np/files/2013/01/030404_Romo_D1.jpg"><img class="alignright size-full wp-image-1156" title="030404_Romo_D[1]" src="http://blogs.rsc.org/np/files/2013/01/030404_Romo_D1.jpg" alt="" width="182" height="242" /></a>Daniel Romo received his B.A. in chemistry/biology from Texas A&amp;M and a PhD in Chemistry from Colorado State University as a NSF Minority Graduate Fellow under the tutelage of the late Prof. Albert I. Meyers. Following postdoctoral studies at Harvard as an American Cancer Society Fellow, with Prof. Stuart L. Schreiber, he began his independent career at TexasA&amp;M in 1993 and is currently Professor of Chemistry and Director of the Natural Products LINCPHIN Laboratory (TAMU).</p>
<p>Research interests in the Romo Group are at the interface of chemistry and biology focused on total synthesis and biomechanistic studies of natural products and the asymmetric synthesis and application of beta-lactones in organic synthesis and as potential drug candidates. This search led Romo to examine marine specimens &#8211;  many recent bioactive molecules have been discovered in marine species that are now making their way to the clinic.<br />
Romo sees natural products as playgrounds for developing new synthetic strategies and making related compounds with potentially important therapeutic applications. Natural products are keys to cell biology, and he is working to build the bridge between synthesis and biology.</p>
<p><em>&#8216;If I couldn&#8217;t be dreaming up ways to make natural products, I would want to be diving to isolate those natural products and fishing from the deck on my off time!&#8217;</em> says Daniel.</p>
<p><a href="http://blogs.rsc.org/np/files/2013/01/GACAAUW8HO.gif"><img class="alignleft size-full wp-image-1153" title="GACAAUW8HO" src="http://blogs.rsc.org/np/files/2013/01/GACAAUW8HO.gif" alt="" width="106" height="140" /></a>Why not read Daniel Romo&#8217;s latest <em>NPR</em> review article:</p>
<p><strong><a href="http://pubs.rsc.org/en/content/articlelanding/2011/np/c0np00013b">Biosynthesis, asymmetric synthesis, and pharmacology, including cellular targets, of the pyrrole-2-aminoimidazole marine alkaloids<br />
</a></strong>Ali Al-Mourabit, Manuel A. Zancanella, Supriya Tilvi and Daniel Romo<br />
<strong>DOI: </strong>10.1039/C0NP00013B</p>
<div> </div>
<div><em>NPR</em> benefits from the expertise of exceptional scientists guiding the development of the journal. Do you know who they are? <a href="http://www.rsc.org/publishing/journals/np/staff.asp"><strong>Find out more</strong> </a>on our Editorial and Advisory Board members.</div>
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		<title>Meet the NPR Editorial team – see where and when you can meet us in 2013</title>
		<link>http://blogs.rsc.org/np/2013/01/03/meet-the-npr-editorial-team-%e2%80%93-see-where-and-when-you-can-meet-us-in-2013/</link>
		<comments>http://blogs.rsc.org/np/2013/01/03/meet-the-npr-editorial-team-%e2%80%93-see-where-and-when-you-can-meet-us-in-2013/#comments</comments>
		<pubDate>Thu, 03 Jan 2013 15:32:13 +0000</pubDate>
		<dc:creator>Marie Cote, Deputy Editor</dc:creator>
				<category><![CDATA[Conferences]]></category>
		<category><![CDATA[NPR]]></category>

		<guid isPermaLink="false">http://blogs.rsc.org/np/?p=1146</guid>
		<description><![CDATA[The Natural Product Reports Editorial team will be attending a number of conferences in 2013 and we would be delighted to meet you there.  


We’re also the team behind NPR’s sister journals Organic &#38; Biomolecular Chemistry, MedChemComm, and the latest addition to the portfolio, Toxicology Research, so we’ll happily discuss your interdisciplinary research work. In fact, many of our authors choose to publish [...]]]></description>
			<content:encoded><![CDATA[<p>The <a href="http://pubs.rsc.org/en/journals/journalissues/np"><em><strong>Natural Product Reports</strong></em> </a>Editorial team will be attending a number of conferences in 2013 and we would be delighted to meet you there.  </p>
<p style="text-align: center"><a href="http://blogs.rsc.org/md/files/2013/01/Untitled-1.png"><img class="aligncenter" title="Untitled-1" src="http://blogs.rsc.org/md/files/2013/01/Untitled-1.png" alt="" width="376" height="219" /></a></p>
<p><a href="http://blogs.rsc.org/md/files/2013/01/SynthOrg-Editors.jpg"></a></p>
<p>We’re also the team behind <em>NPR’s</em> sister journals <strong><em><a href="http://pubs.rsc.org/en/journals/journalissues/ob">Organic &amp; Biomolecular Chemistry</a></em></strong>, <em><strong><a href="http://pubs.rsc.org/en/Journals/JournalIssues/MD">MedChemComm</a></strong></em>, and the latest addition to the portfolio, <em><strong><a href="http://pubs.rsc.org/en/journals/journalissues/tx">Toxicology Research</a></strong></em>, so we’ll happily discuss your interdisciplinary research work. In fact, many of our authors choose to publish their research across all of these titles.    </p>
<p><strong>Here are just some of the conferences where you can meet us in the coming months:</strong>  </p>
<p>• <strong><a href="http://www.rsc.org/ConferencesAndEvents/RSCConferences/RSCIndiaRoadshow2013/index.asp"><span style="font-size: small">RSC India Roadshow</span></a></strong>, visiting Kolkata, Pune and Bangalore – 5-11 February 2013, India – <a href="http://www.rsc.org/ConferencesAndEvents/RSCConferences/RSCIndiaRoadshow2013/index.asp">View the full details</a>, including the confirmed speakers’ list– <em>Meet Richard</em><br />
• <a href="http://www.toxicology.org/AI/MEET/AM2013/index.asp"><strong><span style="font-size: small">Society of Toxicology’s 52nd Annual Meeting</span></strong></a><span style="font-size: small"> </span>–10-14 March 2013, San Antonio, Texas, USA – <em>Meet Marie</em><br />
• <a href="http://www.rsc.org/Membership/Networking/InterestGroups/Heterocyclic/HeterocyclicMeetings.asp"><strong><span style="font-size: small">40th Lakeland Heterocyclic meeting</span></strong></a><span style="font-size: small"> </span>– 9-13 May 2013, Grasmere, UK – <em>Meet Marie</em><br />
• <a href="http://wizard.musc.edu/frontiers2013.html"><span style="font-size: small"><strong>Frontiers in Medicinal Chemistry</strong> (EFMC)</span></a> - 23-26 June 2013, San Francisco, USA – <em>Meet Richard<br />
</em>• <a href="http://www.indiana.edu/~ismsc8/"><span style="font-size: small"><strong>8-ISMSC</strong> </span></a>(International Symposium on Macrocyclic and Supramolecular Chemistry) – 07-11 July 2013, Washington DC, USA – <em>Meet Richard<br />
</em>• <a href="http://esoc2013.eu/"><span style="font-size: small"><strong>ESOC 2013</strong> </span></a>(8th European Symposium on Organic Chemistry) – 08-12 July 2013, Marseille, France – <em>Meet Marie<br />
</em>• <a href="http://sites.chem.colostate.edu/omcos/OMCOS_17/Welcome.html"><strong><span style="font-size: small">OMCOS 17</span></strong></a><span style="font-size: small"> </span>(IUPAC Conference on Organometallic Chemistry Towards Organic Synthesis)- 28 July to 01 August 2013, Fort Collins, USA – <em>Meet Marie<br />
</em>• <a href="http://www.eurotox2013.com/"><strong><span style="font-size: small">EUROTOX 2013</span></strong></a>- 01-04 September 2013, Interlaken, Switzerland – <em>Meet Marie<br />
</em>• <strong><span style="font-size: small">Fall ACS meeting</span></strong>- 08-12 September 2013, Indianapolis, USA – <em>Meet Richard<br />
</em>• <span style="font-size: small"><strong>Asian Medicinal Chemistry Conference</strong> </span>– October 2013, Taipei, Taiwan – <em>Meet Richard<br />
</em>• <a href="http://www.bmos.com.br/arquivos/index.htm"><span style="font-size: small"><strong>15th BMOS</strong> </span></a>- Brazilian Meeting on Organic Synthesis, 10-13 November 2013, Campos do Jordão, Brazil – <em>Meet Richard</em>    </p>
<p style="text-align: center"><a href="mailto:medchemcomm-rsc@rsc.org"><strong>Let us know </strong></a>if you are planning on attending any of these meetings, as it would be lovely to see you there!   </p>
<p><a href="http://blogs.rsc.org/ob/files/2013/01/OBC.gif"><img title="OBC" src="http://blogs.rsc.org/ob/files/2013/01/OBC.gif" alt="" width="104" height="136" /></a>  <a href="http://blogs.rsc.org/ob/files/2013/01/MedChemComm.gif"><img title="MedChemComm" src="http://blogs.rsc.org/ob/files/2013/01/MedChemComm.gif" alt="" width="104" height="136" /></a>  <a href="http://blogs.rsc.org/ob/files/2013/01/NPR.gif"><img title="NPR" src="http://blogs.rsc.org/ob/files/2013/01/NPR.gif" alt="" width="104" height="136" /></a>  <a href="http://blogs.rsc.org/ob/files/2013/01/Toxicology-Research.gif"><img title="Toxicology Research" src="http://blogs.rsc.org/ob/files/2013/01/Toxicology-Research.gif" alt="" width="104" height="136" /></a></p>
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		<title>Ribosomally synthesised natural products: a new name for a new year</title>
		<link>http://blogs.rsc.org/np/2012/12/13/ribosomally-synthesised-natural-products-a-new-name-for-a-new-year/</link>
		<comments>http://blogs.rsc.org/np/2012/12/13/ribosomally-synthesised-natural-products-a-new-name-for-a-new-year/#comments</comments>
		<pubDate>Thu, 13 Dec 2012 10:15:45 +0000</pubDate>
		<dc:creator>James Anson, Deputy Editor</dc:creator>
				<category><![CDATA[Hot articles]]></category>
		<category><![CDATA[MedChemComm]]></category>
		<category><![CDATA[NPR]]></category>
		<category><![CDATA[OBC]]></category>

		<guid isPermaLink="false">http://blogs.rsc.org/np/?p=1136</guid>
		<description><![CDATA[A large collection of leading researchers in the field of natural product synthesis have come together to propose a communal nomenclature system for the biosynthesis of ribosomally synthesised and posttranslationally modified peptides (RiPPs).
The number of ribosomally synthesised natural products is rapidly increasing, and currently there is no uniform nomenclature being applied across the different compound [...]]]></description>
			<content:encoded><![CDATA[<p><a href="http:xlink.rsc.org/?doi=10.1039/C2NP20085F"><img class="alignright" src="http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=C2NP20085F" alt="" width="378" height="157" /></a><em>A large collection of leading researchers in the field of natural product synthesis have come together to <a href="http://xlink.rsc.org/?doi=10.1039/C2NP20085F">propose a communal nomenclature system for the biosynthesis of ribosomally synthesised and posttranslationally modified peptides (RiPPs)</a>.</em></p>
<p>The number of ribosomally synthesised natural products is rapidly increasing, and currently there is no uniform nomenclature being applied across the different compound classes. The classifications currently being used are starting to break down with the increasing number of available genome sequences; the nomenclature used in the various communities investigating subgroups of natural products of ribosomal origin can be confusing, and in some cases even contradictory.</p>
<p>Following on from several discussion groups, the authors of this review (who are working on different classes of RiPPs) present recommendations for a common nomenclature that encompasses all classes, and hope that such a nomenclature will be supported by the rest of the community with the classification of new classes.</p>
<p>In addition to this nomenclature recommendation the authors also present an overview of the current knowledge of the structures and biosynthesis of more than twenty distinct compound classes with examples from bacteria, plants and fungi.</p>
<p>Read this highly informative review today and help sculpt and direct the future of RiPP research.</p>
<p><a href="http://xlink.rsc.org/?doi=10.1039/C2NP20085F"><strong>Ribosomally synthesized and  post-translationally modified peptide natural products: overview and  recommendations for a universal nomenclature</strong></a><br />
<strong>DOI: </strong> 10.1039/C2NP20085F</p>
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		<title>Welcome to NPR issue 1, 2013 &#8211; beta-lactams, flavoenzymes, and much more</title>
		<link>http://blogs.rsc.org/np/2012/12/12/welcome-to-npr-issue-1-2013-beta-lactams-flavoenzymes-and-much-more/</link>
		<comments>http://blogs.rsc.org/np/2012/12/12/welcome-to-npr-issue-1-2013-beta-lactams-flavoenzymes-and-much-more/#comments</comments>
		<pubDate>Wed, 12 Dec 2012 16:53:11 +0000</pubDate>
		<dc:creator>Marie Cote, Deputy Editor</dc:creator>
				<category><![CDATA[News]]></category>
		<category><![CDATA[MedChemComm]]></category>
		<category><![CDATA[NPR]]></category>
		<category><![CDATA[OBC]]></category>

		<guid isPermaLink="false">http://blogs.rsc.org/np/?p=1120</guid>
		<description><![CDATA[Welcome to NPR Issue 1, 2013!
At NPR we&#8217;re kick-starting the New Year with a selection of exciting Highlight and Review articles we think you will like&#8230;
Interested in antibiotics? Read works by Yeo Joon Yoon et al. highlighting aminoglycosides, the review by Christopher J. Schofield et al. on biosynthetic pathways leading to the different classes of β-lactam [...]]]></description>
			<content:encoded><![CDATA[<p style="text-align: center"><a href="http://blogs.rsc.org/np/files/2012/12/GACACGGQ6E.gif"><img class="alignleft size-full wp-image-1121" title="GACACGGQ6E" src="http://blogs.rsc.org/np/files/2012/12/GACACGGQ6E.gif" alt="" width="148" height="194" /></a><strong>Welcome to <a href="http://pubs.rsc.org/en/journals/journalissues/np#!issueid=np030001&amp;type=current&amp;issnprint=0265-0568"><em>NPR</em> Issue 1</a>, 2013!</strong></p>
<p>At <em>NPR</em> we&#8217;re kick-starting the New Year with a selection of exciting Highlight and Review articles we think you will like&#8230;</p>
<p>Interested in antibiotics? Read works by <strong>Yeo Joon Yoon</strong> <em>et al.</em> highlighting <span style="color: #800080"><a href="http://pubs.rsc.org/en/content/articlelanding/2013/np/c2np20092a">aminoglycosides</a></span>, the review by <strong>Christopher J. Schofield </strong><em>et al.</em> on biosynthetic pathways leading to the different classes of <span style="color: #800080"><a href="http://pubs.rsc.org/en/content/articlelanding/2013/np/c2np20065a">β-lactam antibiotics</a></span> (cover article), or learn all about the <span style="color: #800080"><a href="http://pubs.rsc.org/en/content/articlelanding/2013/np/c2np20080e">tiacumicin</a></span> odyssey in this overview by <strong>Jieping Zhu </strong><em>et al.</em> of the chemistry and biology of <a href="http://pubs.rsc.org/en/content/articlelanding/2013/np/c2np20080e">tiacumicins</a> since their discovery to the marketed drug.</p>
<p>Speaking of <span style="color: #800080"><a href="http://pubs.rsc.org/en/content/articlelanding/2013/np/c2np20085f">ribosomally synthesized natural products</a></span>? <strong>Wilfred van der Donk </strong>led an impressive international multiauthored article on establishing a uniform and readily recognized nomenclature for ribosomally synthesized and posttranslationally modified natural products. The whole community came together and made a recommendation, the results of which you can read in this article. Read more about it <a href="http://blogs.rsc.org/np/2012/12/13/ribosomally-synthesised-natural-products-a-new-name-for-a-new-year/">in this post</a>.</p>
<p>This issue wouldn&#8217;t be complete without <strong>Christopher Walsh</strong> and Timothy A. Wencewicz&#8217;s work on <span style="color: #800080"><a href="http://pubs.rsc.org/en/content/articlelanding/2013/np/c2np20069d">flavoenzymes</a></span> as versatile catalysts in biosynthetic pathways, that enable the many chemical transformations building complexity in the biosynthesized natural products architecture.</p>
<p style="text-align: center"><strong><span style="color: #008080">All these articles are <span style="text-decoration: underline">Free to Access</span> for an unlimited period  &#8211; enjoy and spread the word! </span></strong></p>
<p><strong> </strong><strong>Want to see your work in <em>NPR</em>?</strong></p>
<p>Reviews, Highlights and Viewpoints in <em>NPR</em> are generally solicited by members of the editorial board; however we are happy to consider submission enquiries from authors. If you are interested in writing an article for <em>NPR</em> please contact the editorial office with a <a href="http://www.rsc.org/publishing/journals/np/about.asp">brief synopsis</a>.</p>
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