Abstract
The Passerini reactions of indane-1,2,3-trione, tosylmethyl isocyanide, and benzoic acid derivatives proceed at room temperature giving sterically congested 2,2-disubstituted indane-1,3-dione derivatives in quantitative yield. The reactions are one-pot, and the products obtained did not require any purification. ©ARKAT-USA, Inc.
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Kazemizadeh, A. R., & Ramazani, A. (2008). Three component reaction of indane-1,2,3-trione, tosylmethyl isocyanide and benzoic acid derivatives. Arkivoc, 2008(15), 159–165. https://doi.org/10.3998/ark.5550190.0009.f15
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