Copper-catalysed dynamic kinetic asymmetric C−O cross-coupling to access chiral aryl oxime ethers and diaryl ethers

Abstract Dynamic kinetic resolution (DKR) has emerged as an elegant and powerful tool for enantioselective synthesis, enabling the transformation of racemic compounds into enantiomerically enriched products with theoretically quantitative yields. Despite its widespread success, the dynamic kinetic a...

Full description

Saved in:
Bibliographic Details
Main Authors: Mei-Ru Zhang, Hao-Ran Wang, Hui-Mei Shan, Long-Long Xi, Chuan-Jun Lu, Xiao-Man Du, Che Sun, Li-Ping Xu, Ren-Rong Liu
Format: Article
Language:English
Published: Nature Portfolio 2025-03-01
Series:Nature Communications
Online Access:https://doi.org/10.1038/s41467-025-57804-8
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Abstract Dynamic kinetic resolution (DKR) has emerged as an elegant and powerful tool for enantioselective synthesis, enabling the transformation of racemic compounds into enantiomerically enriched products with theoretically quantitative yields. Despite its widespread success, the dynamic kinetic asymmetric C−O cross-coupling has presented significant challenges and remains unexplored. In this study, we report a dynamic kinetic asymmetric C−O cross-coupling of oximes and phenols via copper/BOX-catalysed enantioselective O-arylation with diaryliodonium salts. This method efficiently produces a wide range of inherently chiral oxime ethers, as well as axially chiral styrenes, with high yields and excellent regio- and enantioselectivities. Through controlled experiments and Density Functional Theory (DFT) studies, we have elucidated the dynamic kinetic resolution process and gained insights into the origins of regio- and enantioselectivity.
ISSN:2041-1723