Issue 18, 2015

Palladium-catalyzed carbonylative Sonogashira coupling between aryl triazenes and alkynes

Abstract

We developed a palladium-catalyzed carbonylative Sonogashira reaction with aryl triazenes and alkynes as substrates and methanesulfonic acid as the additive. A series of α,β-ynones were synthesized by this alternative procedure. Notably, bromides, iodides and hydroxyl groups could be well-tolerated under these reaction conditions.

Graphical abstract: Palladium-catalyzed carbonylative Sonogashira coupling between aryl triazenes and alkynes

Supplementary files

Article information

Article type
Communication
Submitted
13 Mar 2015
Accepted
27 Mar 2015
First published
27 Mar 2015

Org. Biomol. Chem., 2015,13, 5090-5093

Author version available

Palladium-catalyzed carbonylative Sonogashira coupling between aryl triazenes and alkynes

W. Li and X. Wu, Org. Biomol. Chem., 2015, 13, 5090 DOI: 10.1039/C5OB00502G

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