Issue 12, 2006

Carboxylative cyclization of propargylamines with supercritical carbon dioxide

Abstract

Propargylic amines were found to react smoothly with carbon dioxide under supercritical conditions to give (Z)-5-alkylidene-1,3-oxazolidin-2-ones exclusively, even in the absence of any metal or base catalyst.

Graphical abstract: Carboxylative cyclization of propargylamines with supercritical carbon dioxide

Supplementary files

Article information

Article type
Communication
Submitted
13 Mar 2006
Accepted
11 Sep 2006
First published
26 Sep 2006

Green Chem., 2006,8, 1019-1021

Carboxylative cyclization of propargylamines with supercritical carbon dioxide

Y. Kayaki, M. Yamamoto, T. Suzuki and T. Ikariya, Green Chem., 2006, 8, 1019 DOI: 10.1039/B603700C

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