| 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, 
											![First Page Preview: Selective synthesis of 4,5-dihydroimidazo- and imidazo[1,5-a]quinoxalines via modified Pictet-Spengler reaction Selective synthesis of 4,5-dihydroimidazo- and imidazo[1,5-a]quinoxalines via modified Pictet-Spengler reaction](/preview/png/5263960.png)