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	<title>Thiophene cycloadditions &#8211; BIOENGINEER.ORG</title>
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		<title>New Route to Strychnos Alkaloids via Thiophene Cycloadditions</title>
		<link>https://bioengineer.org/new-route-to-strychnos-alkaloids-via-thiophene-cycloadditions/</link>
		
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		<pubDate>Fri, 23 Jan 2026 14:03:45 +0000</pubDate>
				<category><![CDATA[Chemistry]]></category>
		<category><![CDATA[chiral catalysis]]></category>
		<category><![CDATA[Collective asymmetric synthesis]]></category>
		<category><![CDATA[drug discovery]]></category>
		<category><![CDATA[S-dioxide cycloadditions]]></category>
		<category><![CDATA[stereoselective synthesis]]></category>
		<category><![CDATA[Strychnos alkaloids]]></category>
		<category><![CDATA[Synthetic chemistry breakthrough]]></category>
		<category><![CDATA[Thiophene cycloadditions]]></category>
		<category><![CDATA[Thiophene S]]></category>
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					<description><![CDATA[In a groundbreaking advance that reverberates through the realms of synthetic chemistry and natural product synthesis, a team led by K.H. Park, J. Park, and N. Frank has unveiled a novel collective asymmetric synthetic route harnessing thiophene S,S-dioxide cycloadditions to access the complex Strychnos alkaloids. This landmark work, reported in Nature Chemistry, promises to redefine [&#8230;]]]></description>
		
		
		
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