Photoexcited Nickel(0)‐Catalyzed Direct Decarboxylative Cross‐Coupling
Decarboxylative coupling is a key strategy for C─C bond formation in modern synthesis. Despite the abundance and diversity of natural amino acids, their direct decarboxylation remains challenging. Here, we report the direct decarboxylation of amino acids to generate α-aminocarbon radicals and their subsequent cross-coupling, enabled by air-stable nickel(0) complexes under photoexcitation without external photosensitizers. This mild catalytic system shows broad compatibility with diverse amino acids and aromatic functional groups, providing a new approach for their direct decarboxylation and functionalization.
Authors
- Geyang Song
- Juan Fan (ORCID: https://orcid.org/0000-0001-5576-1067)
- Dong Xue (ORCID: https://orcid.org/0000-0002-7269-6356)
- Jingsheng Li (ORCID: https://orcid.org/0009-0003-2152-8752)
- Xiaoli Shi
- Xinyi Liu
- Yi Xiao
Institutions
- Shaanxi Normal University (CN)
Publication Details
- Journal
- Chemistry - A European Journal
- Published
- 2026-06-27
- DOI
- https://doi.org/10.1002/chem.71312
- Primary Topic
- Radical Photochemical Reactions
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- National Natural Science Foundation of China
- Fundamental Research Funds for the Central Universities