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Enantioselective Intramolecular Copper-Catalyzed Borylacylation

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Specialty Chemistry
Date 2018 Aug 31
PMID 30160825
Citations 18
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Abstract

An enantioselective copper-catalyzed intramolecular borylacylation is reported. The reaction proceeds through an initial enantioselective borylcupration of the styrene, followed by a nucleophilic attack on the tethered carbamoyl chloride. The products, chiral borylated 3,3-disubstituted oxindoles, were generated in excellent yields and enantioselectivities. The versatile carbon-boron bond provides a platform for a wide array of diversification.

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