Journal
CATALYSIS COMMUNICATIONS
Volume 56, Issue -, Pages 65-67Publisher
ELSEVIER
DOI: 10.1016/j.catcom.2014.06.028
Keywords
Regioseletive; Palladium-catalyzed; Imidazo[1,2-a]pyridines; Cross-coupling; Arylboronic acids
Categories
Funding
- National Natural Science Foundation of China [21302023, 21272044]
- Department of Education of Guangdong Province [2013kjcx0111]
- Foundation for Distinguished Young Talents in Higher Education of Guangdong, China [2012LYM_0086]
Ask authors/readers for more resources
A highly regioselective method for the palladium-catalyzed direct cross-coupling of imidazo[1,2-a]pyridines with arylboronic acids has been developed by using O-2 as oxidant. This process can be applied to a wide range of imidazo[1,2-a]pyridines and arylboronic acids with excellent C-3-regioselectivity. It provides a new way for developing C-C bond-forming processes of multisubstituted imidazo[1,2-a]pyridines, which are common structural motifs in natural products and pharmaceuticals. (C) 2014 Elsevier B.V. All rights reserved.
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