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	<title>copper-catalyzed redox processes &#8211; BIOENGINEER.ORG</title>
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		<title>Amines Transformed via Boryl Radical Scission</title>
		<link>https://bioengineer.org/amines-transformed-via-boryl-radical-scission/</link>
		
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		<pubDate>Wed, 15 Oct 2025 21:54:44 +0000</pubDate>
				<category><![CDATA[Technology]]></category>
		<category><![CDATA[amine functionalization strategies]]></category>
		<category><![CDATA[boryl radical β-scission]]></category>
		<category><![CDATA[C(sp³)–N bond functionalization]]></category>
		<category><![CDATA[copper-catalyzed redox processes]]></category>
		<category><![CDATA[deaminative cross-coupling]]></category>
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					<description><![CDATA[In a groundbreaking advancement that stands to reshape synthetic organic chemistry, researchers have unveiled a transformative approach to amine chemistry that challenges longstanding paradigms. Amines—ubiquitous functional groups in bioactive compounds and pharmaceuticals—have traditionally been regarded as synthetic endpoints, largely inert once formed. However, an innovative study recently published in Nature introduces a novel strategy that [&#8230;]]]></description>
		
		
		
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