Issue 24, 2019

Palladium-catalyzed carbonylative synthesis of substituted cyclopentenones from aryl iodides and internal alkynes

Abstract

In this Communication, a palladium-catalyzed carbonylative synthesis of substituted cyclopentenones has been developed. With aryl iodides and internal alkynes as the substrates, via a domino process consisting of a formal Pauson–Khand reaction, good yields of the desired products were obtained. Interestingly, formic acid has been used both as a hydrogen source and a carbon monoxide source in this system.

Graphical abstract: Palladium-catalyzed carbonylative synthesis of substituted cyclopentenones from aryl iodides and internal alkynes

Supplementary files

Article information

Article type
Communication
Submitted
03 May 2019
Accepted
16 May 2019
First published
16 May 2019

Org. Biomol. Chem., 2019,17, 5882-5885

Palladium-catalyzed carbonylative synthesis of substituted cyclopentenones from aryl iodides and internal alkynes

J. Peng, W. Wang and X. Wu, Org. Biomol. Chem., 2019, 17, 5882 DOI: 10.1039/C9OB01019J

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