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	<title>Naturalproductman's Blog</title>
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	<description>Hey, is that a natural product?!</description>
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		<title>Naturalproductman's Blog</title>
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		<item>
		<title>Diyne desymmetrization</title>
		<link>http://naturalproductman.wordpress.com/2013/05/21/diyne-desymmetrization/</link>
		<comments>http://naturalproductman.wordpress.com/2013/05/21/diyne-desymmetrization/#comments</comments>
		<pubDate>Tue, 21 May 2013 18:14:05 +0000</pubDate>
		<dc:creator>naturalproductman</dc:creator>
				<category><![CDATA[Alkaloids]]></category>
		<category><![CDATA[Asymmetric]]></category>
		<category><![CDATA[Cascade Reactions]]></category>
		<category><![CDATA[Methodology]]></category>
		<category><![CDATA[Organocatalytic]]></category>

		<guid isPermaLink="false">http://naturalproductman.wordpress.com/?p=8994</guid>
		<description><![CDATA[Ulrich Hennecke and co-workers at the Universitat Munster have reported in JAC on a desymmetrization of a diyne. JACS paper<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=naturalproductman.wordpress.com&#038;blog=6451980&#038;post=8994&#038;subd=naturalproductman&#038;ref=&#038;feed=1" width="1" height="1" />]]></description>
				<content:encoded><![CDATA[<p>Ulrich Hennecke and co-workers at the Universitat Munster have reported in JAC on a desymmetrization of a diyne.</p>
<p><img alt="Diyne" src="http://pubs.acs.org/appl/literatum/publisher/achs/journals/content/jacsat/0/jacsat.ahead-of-print/ja402910d/aop/images/medium/ja-2013-02910d_0006.gif" /></p>
<p><a title="desymmetrization" href="http://pubs.acs.org/doi/abs/10.1021/ja402910d" target="_blank">JACS paper</a></p>
<br />  <a rel="nofollow" href="http://feeds.wordpress.com/1.0/gocomments/naturalproductman.wordpress.com/8994/"><img alt="" border="0" src="http://feeds.wordpress.com/1.0/comments/naturalproductman.wordpress.com/8994/" /></a> <img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=naturalproductman.wordpress.com&#038;blog=6451980&#038;post=8994&#038;subd=naturalproductman&#038;ref=&#038;feed=1" width="1" height="1" />]]></content:encoded>
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			<media:title type="html">naturalproductman</media:title>
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			<media:title type="html">Diyne</media:title>
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	</item>
		<item>
		<title>Desymmetrizing oxetanes</title>
		<link>http://naturalproductman.wordpress.com/2013/05/21/desymmetring-oxetanes/</link>
		<comments>http://naturalproductman.wordpress.com/2013/05/21/desymmetring-oxetanes/#comments</comments>
		<pubDate>Tue, 21 May 2013 14:52:09 +0000</pubDate>
		<dc:creator>naturalproductman</dc:creator>
				<category><![CDATA[Asymmetric]]></category>
		<category><![CDATA[Desymmetrization]]></category>
		<category><![CDATA[Methodology]]></category>

		<guid isPermaLink="false">http://naturalproductman.wordpress.com/?p=8991</guid>
		<description><![CDATA[Jianwei Sun and co-workers from the Hong Kong University of Science and Technology have reported in ACIE on a desymmetrization of oxetanes using a phosphoric acid catalyst. ACIE paper<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=naturalproductman.wordpress.com&#038;blog=6451980&#038;post=8991&#038;subd=naturalproductman&#038;ref=&#038;feed=1" width="1" height="1" />]]></description>
				<content:encoded><![CDATA[<p>Jianwei Sun and co-workers from the Hong Kong University of Science and Technology have reported in ACIE on a desymmetrization of oxetanes using a phosphoric acid catalyst.</p>
<p><img alt="desymmetrization" src="http://onlinelibrary.wiley.com/store/10.1002/anie.201300188/asset/image_n/ncontent.gif?v=1&amp;s=303b497585bd72dd6aa7dfa24da15236cec0641b" /></p>
<p><a title="desymmetrize" href="http://onlinelibrary.wiley.com/doi/10.1002/anie.201300188/abstract" target="_blank">ACIE paper</a></p>
<br />  <a rel="nofollow" href="http://feeds.wordpress.com/1.0/gocomments/naturalproductman.wordpress.com/8991/"><img alt="" border="0" src="http://feeds.wordpress.com/1.0/comments/naturalproductman.wordpress.com/8991/" /></a> <img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=naturalproductman.wordpress.com&#038;blog=6451980&#038;post=8991&#038;subd=naturalproductman&#038;ref=&#038;feed=1" width="1" height="1" />]]></content:encoded>
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		<slash:comments>0</slash:comments>
	
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			<media:title type="html">naturalproductman</media:title>
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			<media:title type="html">desymmetrization</media:title>
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	</item>
		<item>
		<title>Roxbin B</title>
		<link>http://naturalproductman.wordpress.com/2013/05/21/roxbin-b/</link>
		<comments>http://naturalproductman.wordpress.com/2013/05/21/roxbin-b/#comments</comments>
		<pubDate>Tue, 21 May 2013 14:47:35 +0000</pubDate>
		<dc:creator>naturalproductman</dc:creator>
				<category><![CDATA[Glycosides]]></category>
		<category><![CDATA[Methodology]]></category>
		<category><![CDATA[Structural Reassignment]]></category>
		<category><![CDATA[Total Synthesis]]></category>

		<guid isPermaLink="false">http://naturalproductman.wordpress.com/?p=8989</guid>
		<description><![CDATA[Hidetoshi Yamada and co-workers at Kwansei Gakuin University have reported in JOC on a structural reassignment concluding that roxbin B is cuspinin. JOC paper<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=naturalproductman.wordpress.com&#038;blog=6451980&#038;post=8989&#038;subd=naturalproductman&#038;ref=&#038;feed=1" width="1" height="1" />]]></description>
				<content:encoded><![CDATA[<p>Hidetoshi Yamada and co-workers at Kwansei Gakuin University have reported in JOC on a structural reassignment concluding that roxbin B is cuspinin.</p>
<p><img alt="roxbin B" src="http://pubs.acs.org/appl/literatum/publisher/achs/journals/content/joceah/0/joceah.ahead-of-print/jo400562k/aop/images/medium/jo-2013-00562k_0011.gif" /></p>
<p><a title="roxbin B" href="http://pubs.acs.org/doi/abs/10.1021/jo400562k" target="_blank">JOC paper</a></p>
<br />  <a rel="nofollow" href="http://feeds.wordpress.com/1.0/gocomments/naturalproductman.wordpress.com/8989/"><img alt="" border="0" src="http://feeds.wordpress.com/1.0/comments/naturalproductman.wordpress.com/8989/" /></a> <img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=naturalproductman.wordpress.com&#038;blog=6451980&#038;post=8989&#038;subd=naturalproductman&#038;ref=&#038;feed=1" width="1" height="1" />]]></content:encoded>
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		<slash:comments>0</slash:comments>
	
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			<media:title type="html">naturalproductman</media:title>
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			<media:title type="html">roxbin B</media:title>
		</media:content>
	</item>
		<item>
		<title>Long C-O bond</title>
		<link>http://naturalproductman.wordpress.com/2013/05/21/long-c-o-bond/</link>
		<comments>http://naturalproductman.wordpress.com/2013/05/21/long-c-o-bond/#comments</comments>
		<pubDate>Tue, 21 May 2013 11:11:43 +0000</pubDate>
		<dc:creator>naturalproductman</dc:creator>
				<category><![CDATA[Methodology]]></category>

		<guid isPermaLink="false">http://naturalproductman.wordpress.com/?p=8986</guid>
		<description><![CDATA[Mark Mascal and co-workers at UC Davis have published in JACS on a long C-O bond in an oxonium ion. JACS paper<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=naturalproductman.wordpress.com&#038;blog=6451980&#038;post=8986&#038;subd=naturalproductman&#038;ref=&#038;feed=1" width="1" height="1" />]]></description>
				<content:encoded><![CDATA[<p>Mark Mascal and co-workers at UC Davis have published in JACS on a long C-O bond in an oxonium ion.</p>
<p><img alt="ion" src="http://pubs.acs.org/appl/literatum/publisher/achs/journals/content/jacsat/0/jacsat.ahead-of-print/ja4032715/aop/images/medium/ja-2013-032715_0008.gif" /></p>
<p><a title="oxonium" href="http://pubs.acs.org/doi/abs/10.1021/ja4032715" target="_blank">JACS paper</a></p>
<br />  <a rel="nofollow" href="http://feeds.wordpress.com/1.0/gocomments/naturalproductman.wordpress.com/8986/"><img alt="" border="0" src="http://feeds.wordpress.com/1.0/comments/naturalproductman.wordpress.com/8986/" /></a> <img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=naturalproductman.wordpress.com&#038;blog=6451980&#038;post=8986&#038;subd=naturalproductman&#038;ref=&#038;feed=1" width="1" height="1" />]]></content:encoded>
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		<slash:comments>0</slash:comments>
	
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			<media:title type="html">naturalproductman</media:title>
		</media:content>

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			<media:title type="html">ion</media:title>
		</media:content>
	</item>
		<item>
		<title>Spectral Database for Instructors</title>
		<link>http://naturalproductman.wordpress.com/2013/05/20/spectral-database-for-instructors/</link>
		<comments>http://naturalproductman.wordpress.com/2013/05/20/spectral-database-for-instructors/#comments</comments>
		<pubDate>Mon, 20 May 2013 21:02:44 +0000</pubDate>
		<dc:creator>naturalproductman</dc:creator>
				<category><![CDATA[Random]]></category>

		<guid isPermaLink="false">http://naturalproductman.wordpress.com/?p=8982</guid>
		<description><![CDATA[Andrew Harned&#8217;s group in Minnesota has put up a site on spectral database for instructors. It would be useful for any chemist if they wanted to find the FID for any NMR spectrum of a compound they are trying to make.  I think this would be actually a good idea to have for any compound [&#8230;]<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=naturalproductman.wordpress.com&#038;blog=6451980&#038;post=8982&#038;subd=naturalproductman&#038;ref=&#038;feed=1" width="1" height="1" />]]></description>
				<content:encoded><![CDATA[<p>Andrew Harned&#8217;s group in Minnesota has put up a site on <a title="SDI" href="http://harned.chem.umn.edu/" target="_blank">spectral database for instructors</a>. It would be useful for any chemist if they wanted to find the FID for any NMR spectrum of a compound they are trying to make.  I think this would be actually a good idea to have for any compound in general as proof of compound synthesized.  It would be nice if we don&#8217;t have to be instructors to use it though.</p>
<p><a title="SDI" href="http://pubs.acs.org/doi/abs/10.1021/ed300787v" target="_blank">JCE paper</a></p>
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		<slash:comments>0</slash:comments>
	
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			<media:title type="html">naturalproductman</media:title>
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		<item>
		<title>Dictyostatin synthesis</title>
		<link>http://naturalproductman.wordpress.com/2013/05/17/dictyostatin-synthesis/</link>
		<comments>http://naturalproductman.wordpress.com/2013/05/17/dictyostatin-synthesis/#comments</comments>
		<pubDate>Fri, 17 May 2013 21:15:51 +0000</pubDate>
		<dc:creator>naturalproductman</dc:creator>
				<category><![CDATA[Macrolides]]></category>
		<category><![CDATA[Methodology]]></category>
		<category><![CDATA[Total Synthesis]]></category>

		<guid isPermaLink="false">http://naturalproductman.wordpress.com/?p=8980</guid>
		<description><![CDATA[James Leighton and co-workers have reported in ACIE on the synthesis of dictyostatin. ACIE paper<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=naturalproductman.wordpress.com&#038;blog=6451980&#038;post=8980&#038;subd=naturalproductman&#038;ref=&#038;feed=1" width="1" height="1" />]]></description>
				<content:encoded><![CDATA[<p>James Leighton and co-workers have reported in ACIE on the synthesis of dictyostatin.</p>
<p><img alt="dictyostatin" src="http://onlinelibrary.wiley.com/store/10.1002/anie.201302565/asset/image_n/ncontent.gif?v=1&amp;s=d35d1aebe84de402196aa835cf283cc68abc6af7" /></p>
<p><a title="dictyostatin" href="http://onlinelibrary.wiley.com/doi/10.1002/anie.201302565/abstract" target="_blank">ACIE paper</a></p>
<br />  <a rel="nofollow" href="http://feeds.wordpress.com/1.0/gocomments/naturalproductman.wordpress.com/8980/"><img alt="" border="0" src="http://feeds.wordpress.com/1.0/comments/naturalproductman.wordpress.com/8980/" /></a> <img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=naturalproductman.wordpress.com&#038;blog=6451980&#038;post=8980&#038;subd=naturalproductman&#038;ref=&#038;feed=1" width="1" height="1" />]]></content:encoded>
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		<slash:comments>0</slash:comments>
	
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			<media:title type="html">naturalproductman</media:title>
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		<media:content url="http://onlinelibrary.wiley.com/store/10.1002/anie.201302565/asset/image_n/ncontent.gif?v=1&#38;s=d35d1aebe84de402196aa835cf283cc68abc6af7" medium="image">
			<media:title type="html">dictyostatin</media:title>
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	</item>
		<item>
		<title>BE-43472B synthesis</title>
		<link>http://naturalproductman.wordpress.com/2013/05/17/be-43472b-synthesis/</link>
		<comments>http://naturalproductman.wordpress.com/2013/05/17/be-43472b-synthesis/#comments</comments>
		<pubDate>Fri, 17 May 2013 21:14:06 +0000</pubDate>
		<dc:creator>naturalproductman</dc:creator>
				<category><![CDATA[Antibiotics]]></category>
		<category><![CDATA[Methodology]]></category>
		<category><![CDATA[Total Synthesis]]></category>

		<guid isPermaLink="false">http://naturalproductman.wordpress.com/?p=8978</guid>
		<description><![CDATA[Keisuke Suzuki and co-workers at Tokyo Institute of Technology have reported in ACIE on the synthesis of ACIE paper<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=naturalproductman.wordpress.com&#038;blog=6451980&#038;post=8978&#038;subd=naturalproductman&#038;ref=&#038;feed=1" width="1" height="1" />]]></description>
				<content:encoded><![CDATA[<p>Keisuke Suzuki and co-workers at Tokyo Institute of Technology have reported in ACIE on the synthesis of</p>
<p><img alt="antibiotic" src="http://onlinelibrary.wiley.com/store/10.1002/anie.201301591/asset/image_n/ncontent.gif?v=1&amp;s=466e9230474aad633acadbb445fe8d3a4a21b309" /></p>
<p><a title="BE-43472B" href="http://onlinelibrary.wiley.com/doi/10.1002/anie.201301591/abstract" target="_blank">ACIE paper</a></p>
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		<slash:comments>0</slash:comments>
	
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			<media:title type="html">naturalproductman</media:title>
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			<media:title type="html">antibiotic</media:title>
		</media:content>
	</item>
		<item>
		<title>Transtaganolide syntheses</title>
		<link>http://naturalproductman.wordpress.com/2013/05/17/transtaganolide-syntheses/</link>
		<comments>http://naturalproductman.wordpress.com/2013/05/17/transtaganolide-syntheses/#comments</comments>
		<pubDate>Fri, 17 May 2013 21:11:35 +0000</pubDate>
		<dc:creator>naturalproductman</dc:creator>
				<category><![CDATA[Asymmetric]]></category>
		<category><![CDATA[Cascade Reactions]]></category>
		<category><![CDATA[Claisen rearrangement]]></category>
		<category><![CDATA[Diels-Alder]]></category>
		<category><![CDATA[Methodology]]></category>
		<category><![CDATA[Named Reactions]]></category>
		<category><![CDATA[Sesquiterpenes]]></category>
		<category><![CDATA[Total Synthesis]]></category>

		<guid isPermaLink="false">http://naturalproductman.wordpress.com/?p=8976</guid>
		<description><![CDATA[Brian Stoltz and co-workers have reported in ACIE on the syntheses of transtaganolides through an Ireland-Claisen rearrangement/Diels-Alder cascade. ACIE paper<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=naturalproductman.wordpress.com&#038;blog=6451980&#038;post=8976&#038;subd=naturalproductman&#038;ref=&#038;feed=1" width="1" height="1" />]]></description>
				<content:encoded><![CDATA[<p>Brian Stoltz and co-workers have reported in ACIE on the syntheses of transtaganolides through an Ireland-Claisen rearrangement/Diels-Alder cascade.</p>
<p><img alt="ICR/DA" src="http://onlinelibrary.wiley.com/store/10.1002/anie.201301212/asset/image_n/ncontent.gif?v=1&amp;s=617cabce475a9af8dcd6d5351077014cee3ed154" /></p>
<p><a title="transtaganolide" href="http://onlinelibrary.wiley.com/doi/10.1002/anie.201301212/abstract" target="_blank">ACIE paper</a></p>
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			<media:title type="html">naturalproductman</media:title>
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			<media:title type="html">ICR/DA</media:title>
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		<item>
		<title>Mbandakamines A and B</title>
		<link>http://naturalproductman.wordpress.com/2013/05/16/mbandakamines-a-and-b/</link>
		<comments>http://naturalproductman.wordpress.com/2013/05/16/mbandakamines-a-and-b/#comments</comments>
		<pubDate>Thu, 16 May 2013 12:25:27 +0000</pubDate>
		<dc:creator>naturalproductman</dc:creator>
				<category><![CDATA[Alkaloids]]></category>
		<category><![CDATA[Diseases]]></category>
		<category><![CDATA[Malaria]]></category>

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		<description><![CDATA[Gerhard Bringmann and co-workers at the University of Wurzberg have reported in OL on the isolation of anti-malarial mbandakamines A and B. OL paper<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=naturalproductman.wordpress.com&#038;blog=6451980&#038;post=8973&#038;subd=naturalproductman&#038;ref=&#038;feed=1" width="1" height="1" />]]></description>
				<content:encoded><![CDATA[<p>Gerhard Bringmann and co-workers at the University of Wurzberg have reported in OL on the isolation of anti-malarial mbandakamines A and B.<br />
<img alt="mbandakamines" src="http://pubs.acs.org/appl/literatum/publisher/achs/journals/content/orlef7/0/orlef7.ahead-of-print/ol4005883/aop/images/medium/ol-2013-005883_0006.gif" /></p>
<p><a title="mbandakamines A and B" href="http://pubs.acs.org/doi/abs/10.1021/ol4005883" target="_blank">OL paper</a></p>
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			<media:title type="html">naturalproductman</media:title>
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		<media:content url="http://pubs.acs.org/appl/literatum/publisher/achs/journals/content/orlef7/0/orlef7.ahead-of-print/ol4005883/aop/images/medium/ol-2013-005883_0006.gif" medium="image">
			<media:title type="html">mbandakamines</media:title>
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		<title>Cinchona alkaloid catalyzed proton transfer</title>
		<link>http://naturalproductman.wordpress.com/2013/05/14/cinchona-alkaloid-catalyzed-proton-transfer/</link>
		<comments>http://naturalproductman.wordpress.com/2013/05/14/cinchona-alkaloid-catalyzed-proton-transfer/#comments</comments>
		<pubDate>Tue, 14 May 2013 15:02:19 +0000</pubDate>
		<dc:creator>naturalproductman</dc:creator>
				<category><![CDATA[Asymmetric]]></category>
		<category><![CDATA[Methodology]]></category>
		<category><![CDATA[Organocatalytic]]></category>

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		<description><![CDATA[Jin-Pei Cheng and co-workers from Nankai University have reported in JACS on a biomimetic proton transfer. JACS paper<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=naturalproductman.wordpress.com&#038;blog=6451980&#038;post=8970&#038;subd=naturalproductman&#038;ref=&#038;feed=1" width="1" height="1" />]]></description>
				<content:encoded><![CDATA[<p>Jin-Pei Cheng and co-workers from Nankai University have reported in JACS on a biomimetic proton transfer.</p>
<p><img alt="biomimetic" src="http://pubs.acs.org/appl/literatum/publisher/achs/journals/content/jacsat/0/jacsat.ahead-of-print/ja309133z/aop/images/medium/ja-2012-09133z_0013.gif" /></p>
<p><a title="biomimetic" href="http://pubs.acs.org/doi/abs/10.1021/ja309133z" target="_blank">JACS paper</a></p>
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			<media:title type="html">naturalproductman</media:title>
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			<media:title type="html">biomimetic</media:title>
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