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Tandem cycloaddition–decarboxylation of α-keto acid and isocyanide under oxidant-free conditions towards monosubstituted oxazoles†
Ling-Juan Zhang,Mei-Chen Xu,Jie Liu,Xian-Ming Zhang
RSC Advances Pub Date : 07/26/2016 00:00:00 , DOI:10.1039/C6RA16031J
Abstract

An efficient method, tandem [3 + 2] cycloaddition–decarboxylation of α-keto acid and isocyanide promoted by copper salt, has been developed. Under oxidant-free conditions, a series monosubstituted oxazoles have been constructed. Different from the traditional application of α-oxo acids as acyl surrogates, the elegant approach herein ingeniously avoids consuming excess oxidants.

Graphical abstract: Tandem cycloaddition–decarboxylation of α-keto acid and isocyanide under oxidant-free conditions towards monosubstituted oxazoles
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