Carbamoyl Fluoride-Enabled Enantioselective Ni-Catalyzed Carbocarbamoylation of Unactivated Alkenes

Autor: Shao-Long Qi, Rong-Hua Wang, Mengchun Ye, Feng-Ping Zhang, Yu-Xin Luan, Yue Li
Rok vydání: 2020
Předmět:
Zdroj: Journal of the American Chemical Society. 142:19844-19849
ISSN: 1520-5126
0002-7863
DOI: 10.1021/jacs.0c09949
Popis: A carbamoyl fluoride-enabled enantioselective Ni-catalyzed carbocarbamoylation of unactivated alkenes was developed, providing a broad range of chiral γ-lactams bearing an all-carbon quaternary center in 45-96% yield and 38-97% ee.
Databáze: OpenAIRE