Photoinduced Sulfinate‐Mediated Decarboxylative Heteroarylation of α‐Amino Acid Derivatives

A mild and efficient photoinduced sulfinate‐mediated decarboxylative heteroarylation protocol has been developed for the coupling of α‐amino acid derivatives with 2‐chlorobenzothiazoles. In this report, we developed a low‐cost sulfinate catalytic system as a complementary alternative to conventional Ir/Ni dual catalysis. Notably, this catalytic system was also applicable to the α‐heteroarylation of amines. This method exhibits a broad substrate scope, mild reaction conditions, and simple operation, furnishing a practical strategy for the synthesis of α‐heteroaryl amines. Furthermore, several of the synthesized products showed antiproliferative activity against a variety of cancer cell lines.

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Publication Details

Journal
Advanced Synthesis & Catalysis
Published
2026-06-24
DOI
https://doi.org/10.1002/adsc.70608
Primary Topic
Sulfur-Based Synthesis Techniques
Type
article
Field-Weighted Citation Impact
0.00

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article

Photoinduced Sulfinate‐Mediated Decarboxylative Heteroarylation of α‐Amino Acid Derivatives

Xiaodong Tang, J N Li, Xiaofeng Wu, Weiya Kong et al.
Advanced Synthesis & Catalysis
Sulfur-Based Synthesis Techniques
article

Photoinduced Sulfinate‐Mediated Decarboxylative Heteroarylation of α‐Amino Acid Derivatives

Xiaodong Tang, J N Li, Xiaofeng Wu, Weiya Kong, Yi-Xiang Wang, Jie Shi, Jianuo Chen
article en

Abstract

A mild and efficient photoinduced sulfinate‐mediated decarboxylative heteroarylation protocol has been developed for the coupling of α‐amino acid derivatives with 2‐chlorobenzothiazoles. In this report, we developed a low‐cost sulfinate catalytic system as a complementary alternative to conventional Ir/Ni dual catalysis. Notably, this catalytic system was also applicable to the α‐heteroarylation of amines. This method exhibits a broad substrate scope, mild reaction conditions, and simple operation, furnishing a practical strategy for the synthesis of α‐heteroaryl amines. Furthermore, several of the synthesized products showed antiproliferative activity against a variety of cancer cell lines.

Advanced Synthesis & CatalysisVol. 368(13)
Guangdong Pharmaceutical University (CN), Guangzhou Experimental Station (CN), Southern Medical University (CN)
Basic and Applied Basic Research Foundation of Guangdong Province
Good health and well-being
Openalex Percentile: Top 13%
Sulfur-Based Synthesis Techniques
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