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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

期刊

JOURNAL OF THE BRAZILIAN CHEMICAL SOCIETY
卷 20, 期 2, 页码 309-312

出版社

SOC BRASILEIRA QUIMICA
DOI: 10.1590/S0103-50532009000200016

关键词

indane-1,2,3-trione; isocyanide; Passerini reaction; benzoic acid

资金

  1. Zanjan University

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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.

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