Issue 20, 2021

Enantioselective synthesis of 3-aryl-phthalides through a nickel-catalyzed stereoconvergent cross-coupling reaction

Abstract

A nickel-catalyzed asymmetric Suzuki–Miyaura cross-coupling of racemic 3-bromo-phthalides and arylboronic acids was realized for the synthesis of diverse chiral 3-aryl-phthalides in moderate to excellent reaction yields. The reaction proceeded in a stereoconvergent manner and high enantioselectivities were observed for most examined examples. A number of functional groups like aldehyde, ester and bromide were well tolerated. Heteroaromatic boronic acids were also competent coupling partners in this reaction.

Graphical abstract: Enantioselective synthesis of 3-aryl-phthalides through a nickel-catalyzed stereoconvergent cross-coupling reaction

Supplementary files

Article information

Article type
Communication
Submitted
12 Mar 2021
Accepted
26 Apr 2021
First published
27 Apr 2021

Org. Biomol. Chem., 2021,19, 4492-4496

Enantioselective synthesis of 3-aryl-phthalides through a nickel-catalyzed stereoconvergent cross-coupling reaction

S. Xu, R. Zhang, S. Zhang and C. Feng, Org. Biomol. Chem., 2021, 19, 4492 DOI: 10.1039/D1OB00487E

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