Cost-effective chiral auxiliary-assisted remote asymmetric C(sp3)–H alkylation of hydroxamic acid derivatives with glycine derivatives

Abstract

Visible-light-mediated commercially available and cost-effective chiral auxiliary-assisted radical–radical cross-coupling for the preparation of noncanonical chiral amino acids under base- and metal-free conditions has been reported. The reaction featured a broad substrate scope and excellent enantioselectivity. Besides, the products can be converted to biologically important chiral β-amino alcohols under simple procedures.

Graphical abstract: Cost-effective chiral auxiliary-assisted remote asymmetric C(sp3)–H alkylation of hydroxamic acid derivatives with glycine derivatives

Supplementary files

Article information

Article type
Paper
Submitted
20 May 2025
Accepted
03 Jul 2025
First published
17 Jul 2025

Catal. Sci. Technol., 2025, Advance Article

Cost-effective chiral auxiliary-assisted remote asymmetric C(sp3)–H alkylation of hydroxamic acid derivatives with glycine derivatives

Z. Yang, L. Li, J. Chen, J. Hou, H. Fan, X. Zhang, G. Lv and Y. Wu, Catal. Sci. Technol., 2025, Advance Article , DOI: 10.1039/D5CY00604J

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