Issue 57, 2025

Visible-light-driven decarboxylative C(sp3)–H alkylation of glycine derivatives via in situ formation of NHPI esters

Abstract

A visible-light-driven decarboxylative C(sp3)–H alkylation of glycine derivatives via in situ formation of NHPI esters is reported. The use of the Xantphos/ICH2CH2I system as a dual activator and a catalyst eliminates the need for expensive photocatalysts and transition metals. Under mild conditions, a versatile platform is established for synthesizing unnatural amino acids from readily available alkyl carboxylic acids with high functional group tolerance.

Graphical abstract: Visible-light-driven decarboxylative C(sp3)–H alkylation of glycine derivatives via in situ formation of NHPI esters

Supplementary files

Article information

Article type
Communication
Submitted
28 ៤ 2025
Accepted
06 ៦ 2025
First published
09 ៦ 2025

Chem. Commun., 2025,61, 10558-10561

Visible-light-driven decarboxylative C(sp3)–H alkylation of glycine derivatives via in situ formation of NHPI esters

L. Yang, Y. Tang, S. Gao and P. Zhang, Chem. Commun., 2025, 61, 10558 DOI: 10.1039/D5CC02375K

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