Journal
ORGANIC LETTERS
Volume 6, Issue 5, Pages 843-846Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ol0498803
Keywords
-
Categories
Ask authors/readers for more resources
A one-pot synthesis of substituted imidazoles is described. The cornerstone of this methodology involves the thiazolium-catalyzed addition of an aldehyde to an acyl Imine to generate the corresponding alpha-ketoamide in situ followed by ring closure to the imidazole in a one-pot sequence. The extension of this methodology to the one-pot synthesis of substituted oxazoles and thiazoles is also described.
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