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	<title>remote stereochemical control &#8211; BIOENGINEER.ORG</title>
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	<title>remote stereochemical control &#8211; BIOENGINEER.ORG</title>
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		<title>Precise 1,3-Hydrofunctionalization of Trisubstituted Alkenes</title>
		<link>https://bioengineer.org/precise-13-hydrofunctionalization-of-trisubstituted-alkenes/</link>
		
		<dc:creator><![CDATA[Bioengineer]]></dc:creator>
		<pubDate>Thu, 18 Sep 2025 13:41:48 +0000</pubDate>
				<category><![CDATA[Chemistry]]></category>
		<category><![CDATA[3-hydrofunctionalization]]></category>
		<category><![CDATA[asymmetric catalysis]]></category>
		<category><![CDATA[Catalytic 1]]></category>
		<category><![CDATA[Directing relay mechanism]]></category>
		<category><![CDATA[Enantioselective C–H activation]]></category>
		<category><![CDATA[Remote stereocenter formation]]></category>
		<category><![CDATA[remote stereochemical control]]></category>
		<category><![CDATA[trisubstituted alkene functionalization]]></category>
		<category><![CDATA[Trisubstituted alkenes]]></category>
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					<description><![CDATA[In the vast and ever-evolving landscape of synthetic organic chemistry, the ability to selectively construct complex molecular architectures with precise control over stereochemistry remains one of the grand challenges. Among the myriad transformations designed to forge carbon-heteroatom (C–X) bonds, catalytic hydrofunctionalization of alkenes stands out as a fundamental and versatile approach widely exploited to assemble [&#8230;]]]></description>
		
		
		
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