Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5263960 | Tetrahedron Letters | 2013 | 52 Pages |
Abstract
An efficient tandem approach for the selective synthesis of dihydroimidazo[1,5-a]quinoxalines 6a-g and imidazo[1,5-a]quinoxalines 7a-h by the reaction of 2-imidazolyl anilines 4a-c with aryl aldehydes 5a-k under mild reaction condition is described. Introduction of electron-releasing alkyl groups in substrate 4a-b was found instrumental for the success of the reaction.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Akhilesh Kumar Verma, Rajeev Ranjan Jha, V. Kasi Sankar, Raj Pal Singh,