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.
Authors
- Xiaodong Tang (ORCID: https://orcid.org/0000-0002-0051-105X)
- J N Li
- Xiaofeng Wu (ORCID: https://orcid.org/0000-0001-5549-8836)
- Weiya Kong
- Yi-Xiang Wang (ORCID: https://orcid.org/0000-0002-4021-4228)
- Jie Shi (ORCID: https://orcid.org/0000-0002-1068-5109)
- Jianuo Chen
Institutions
- Guangdong Pharmaceutical University (CN)
- Guangzhou Experimental Station (CN)
- Southern Medical University (CN)
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
Funders
- Basic and Applied Basic Research Foundation of Guangdong Province