Issue 17, 2019

More than a CO source: palladium-catalyzed carbonylative synthesis of butenolides from propargyl alcohols and TFBen

Abstract

Palladium-catalyzed direct carbonylation of propargyl alcohols for the synthesis of butenolides has been achieved. This transformation employs benzene-1,3,5-triyl triformate (TFBen) as the CO source and provides a facile and straightforward access to various substituted butenolides in high yields (up to 85%). Notably, phloroglucinol as the decomposed product of TFBen promotes the formation of butenolides.

Graphical abstract: More than a CO source: palladium-catalyzed carbonylative synthesis of butenolides from propargyl alcohols and TFBen

Supplementary files

Article information

Article type
Research Article
Submitted
18 Jun 2019
Accepted
16 Jul 2019
First published
19 Jul 2019

Org. Chem. Front., 2019,6, 3158-3161

More than a CO source: palladium-catalyzed carbonylative synthesis of butenolides from propargyl alcohols and TFBen

Z. Le, J. Ying and X. Wu, Org. Chem. Front., 2019, 6, 3158 DOI: 10.1039/C9QO00779B

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