Dipolar cycloaddition of ethyl isocyanoacetate to 3-chloro-2-(methylthio)/2-(methylsulfonyl)quinoxalines: highly regio- and chemoselective synthesis of substituted imidazo[1,5-a]quinoxaline-3-carboxylates

Sundaram, G. S. M. ; Singh, B. ; Venkatesh, C. ; Ila, H. ; Junjappa, H. (2007) Dipolar cycloaddition of ethyl isocyanoacetate to 3-chloro-2-(methylthio)/2-(methylsulfonyl)quinoxalines: highly regio- and chemoselective synthesis of substituted imidazo[1,5-a]quinoxaline-3-carboxylates Journal of Organic Chemistry, 72 (13). pp. 5020-5023. ISSN 0022-3263

Full text not available from this repository.

Official URL: http://pubs.acs.org/doi/abs/10.1021/jo070590k

Related URL: http://dx.doi.org/10.1021/jo070590k

Abstract

An efficient route for regio- and chemoselective synthesis of substituted 3-(carboethoxy)imidazo[1,5-a]quinoxalines and novel diimidazo[1,5-a:5',1'-c]quinoxalines via base-induced cycloaddition of ethyl isocyanoacetate to unsymmetrically substituted 3-chloro-2-(methylthio)/2-(methylsulfonyl)quinoxalines has been reported.

Item Type:Article
Source:Copyright of this article belongs to American Chemical Society.
ID Code:15321
Deposited On:13 Nov 2010 12:56
Last Modified:03 Jun 2011 04:38

Repository Staff Only: item control page