Passerini multicomponent reaction of indane-1,2,3-trione: An efficient route for the one-pot synthesis of sterically congested 2,2-disubstituted indane-1,3-dione derivatives

69Citations
Citations of this article
17Readers
Mendeley users who have this article in their library.

Abstract

The Passerini reaction of indane-1,2,3-trione, isocyanides and benzoic acid derivatives proceed at room temperature and sterically congested 2,2-disubstituted indane-1,3-dione derivatives are synthesized in excellent yields. The reaction proceeds smoothly and cleanly under mild conditions and no side reactions are observed. ©2009 Sociedade Brasileira de Química.

Cite

CITATION STYLE

APA

Kazemizadeh, A. R., & Ramazani, A. (2009). Passerini multicomponent reaction of indane-1,2,3-trione: An efficient route for the one-pot synthesis of sterically congested 2,2-disubstituted indane-1,3-dione derivatives. Journal of the Brazilian Chemical Society, 20(2), 309–312. https://doi.org/10.1590/S0103-50532009000200016

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free