Article ID Journal Published Year Pages File Type
5263960 Tetrahedron Letters 2013 52 Pages PDF
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
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