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.
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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
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