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	<title>multicomponent reactions &#8211; BIOENGINEER.ORG</title>
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		<title>Chemists Build a Molecular Sorting Machine to Forge Chiral Amino Alcohols from Simple Feedstocks</title>
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		<pubDate>Wed, 07 Oct 2026 12:36:32 +0000</pubDate>
				<category><![CDATA[Chemistry]]></category>
		<category><![CDATA[1,2-amino alcohols]]></category>
		<category><![CDATA[asymmetric catalysis]]></category>
		<category><![CDATA[chemoselectivity]]></category>
		<category><![CDATA[chiral ligands]]></category>
		<category><![CDATA[enantioselectivity]]></category>
		<category><![CDATA[multicomponent reactions]]></category>
		<category><![CDATA[nucleophile sorting]]></category>
		<category><![CDATA[organic synthesis]]></category>
		<category><![CDATA[palladium catalysis]]></category>
		<category><![CDATA[propargyl-palladium complexes]]></category>
		<category><![CDATA[propargylic carbonates]]></category>
		<category><![CDATA[Synthetic methodology]]></category>
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					<description><![CDATA[A palladium-catalysed nucleophile-sorting strategy enables the one-pot, enantioselective assembly of chiral 1,2-amino alcohols from unprotected amines and alcohols.]]></description>
		
		
		
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