Issue 15, 2022

Palladium-catalyzed intermolecular alkynylcarbonylation of unactivated alkenes: easy access to β-alkynylcarboxylic esters

Abstract

A palladium-catalyzed intermolecular alkynylcarbonylation of unactivated alkenes has been established with ethynyl benziodoxolones (EBXs) as alkynylation reagents, providing β-alkynylcarboxylic esters efficiently from simple alkenes. The reaction features moderate to excellent regioselectivity and excellent functional group compatibility under mild reaction conditions.

Graphical abstract: Palladium-catalyzed intermolecular alkynylcarbonylation of unactivated alkenes: easy access to β-alkynylcarboxylic esters

Supplementary files

Article information

Article type
Communication
Submitted
17 Dec 2021
Accepted
20 Jan 2022
First published
22 Jan 2022

Chem. Commun., 2022,58, 2544-2547

Palladium-catalyzed intermolecular alkynylcarbonylation of unactivated alkenes: easy access to β-alkynylcarboxylic esters

X. Li, P. Chen and G. Liu, Chem. Commun., 2022, 58, 2544 DOI: 10.1039/D1CC07092D

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