期刊
CHEMICAL SCIENCE
卷 10, 期 27, 页码 6666-6671出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c9sc02035g
关键词
-
资金
- JSPS KAKENHI [15H03811]
- MEXT, Japan [18H04259]
- Toray Science Foundation
- Hoansha Foundation
- Program for Leading Graduate Schools: Interactive Materials Science Cadet Program
- Grants-in-Aid for Scientific Research [15H03811, 18H04259] Funding Source: KAKEN
Nickel-catalyzed decarbonylation of N-acylated N-heteroarenes is developed. This method can be used to produce a variety of N-aryl heteroarenes, including pyrroles, indoles, carbazoles and phenoxazines, using benzoic acid derivatives as arylating reagents. Arylnickelamide intermediates that are relevant to the catalytic reaction were characterized by X-ray crystallography. When N-acylated benzimidazoles are used as substrates, decarbonylation accompanied 1,2-migration to form 2-arylated benzimidazoles.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据