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	<title>beta-aminoalkyl radicals &#8211; BIOENGINEER.ORG</title>
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	<title>beta-aminoalkyl radicals &#8211; BIOENGINEER.ORG</title>
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		<title>Borane Trick Cracks Stubborn Aziridines Open for Cleaner Drug Building</title>
		<link>https://bioengineer.org/borane-trick-cracks-stubborn-aziridines-open-for-cleaner-drug-building/</link>
		
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		<pubDate>Thu, 08 Oct 2026 11:10:43 +0000</pubDate>
				<category><![CDATA[Chemistry]]></category>
		<category><![CDATA[aziridines]]></category>
		<category><![CDATA[beta-aminoalkyl radicals]]></category>
		<category><![CDATA[borane coordination]]></category>
		<category><![CDATA[boryl radicals]]></category>
		<category><![CDATA[copper catalysis]]></category>
		<category><![CDATA[cross-coupling]]></category>
		<category><![CDATA[Medicinal Chemistry]]></category>
		<category><![CDATA[nickel catalysis]]></category>
		<category><![CDATA[organic synthesis]]></category>
		<category><![CDATA[photocatalysis]]></category>
		<category><![CDATA[regioselectivity]]></category>
		<category><![CDATA[ring opening]]></category>
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					<description><![CDATA[Chemists have developed a borane-activated radical strategy that opens unactivated N-alkyl aziridines regioselectively and funnels them into copper- and nickel-catalysed cross-couplings, bypassing the need for removable activating groups.]]></description>
		
		
		
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