Journal
RSC ADVANCES
Volume 11, Issue 47, Pages 29372-29375Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/d1ra05936j
Keywords
-
Categories
Funding
- National Natural Science Foundation of Shanghai [1ZR1422600]
- Science and Technology Project of Nantong, China [MS22019026]
- Shanghai Sailing Program [20YF1414100]
Ask authors/readers for more resources
A visible-light-driven cascade radical cyclization process has been established for the synthesis of alpha-carbonyl alkyl-substituted benzimidazo[2,1-alpha]isoquinolin-6(5H)-ones. This protocol offers an efficient and practical method with outstanding yields, mild reaction conditions, and excellent functional group tolerance.
A visible-light-driven cascade radical cyclization process of N-methacryloyl-2-phenylbenzimidazole has been established with alpha-carbonyl alkyl bromide. This protocol provides an efficient and practical method for the synthesis of various alpha-carbonyl alkyl-substituted benzimidazo[2,1-alpha]isoquinolin-6(5H)-ones in outstanding yields, mild reaction conditions and excellent functional group tolerance.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available