Issue 7, 2025

Recyclable g-C3N4 catalyzed decarboxylative alkenylation of N-aryl glycines with vinyl sulfones under visible-light irradiation

Abstract

Allylamines are a versatile class of compounds with significant applications in pharmaceuticals and as building blocks in organic synthesis. Herein we present a straightforward protocol for visible-light driven g-C3N4-catalyzed decarboxylative alkenylation of N-aryl glycines with vinyl sulfones to access allylamines in moderate to excellent yields (up to 91%), and it demonstrated broad substrate compatibility, including primary, secondary, and tertiary N-aryl glycines and diverse vinyl sulfones. Notably, the g-C3N4 catalyst is recyclable up to five times without obvious loss of catalytic performance. Preliminary mechanistic studies indicated that visible light is essential to achieve the desired transformation efficiently.

Graphical abstract: Recyclable g-C3N4 catalyzed decarboxylative alkenylation of N-aryl glycines with vinyl sulfones under visible-light irradiation

Supplementary files

Article information

Article type
Research Article
Submitted
17 Jan 2025
Accepted
11 Feb 2025
First published
14 Feb 2025
This article is Open Access
Creative Commons BY-NC license

Org. Chem. Front., 2025,12, 2409-2414

Recyclable g-C3N4 catalyzed decarboxylative alkenylation of N-aryl glycines with vinyl sulfones under visible-light irradiation

C. Guo, G. Zhao, Y. Feng, D. Chen, T. Loh, D. Wang and Z. Jia, Org. Chem. Front., 2025, 12, 2409 DOI: 10.1039/D5QO00100E

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