Pd-catalyzed highly regioselective olefin isomerization–hydrocarboxylation with formic acid: a facile approach to synthesize linear carboxylic acids from internal olefins

Abstract

Internal olefins can efficiently undergo double bond isomerization and regioselective hydrocarboxylation with HCO2H in the presence of Pd(OAc)2 and 1,2-DTBPMB, providing a wide variety of corresponding linear carboxylic acids bearing various functional groups in good yields and >20 : 1 linear/branch ratios under mild reaction conditions. The reaction is operationally simple and requires no CO gas and acid co-catalysts.

Graphical abstract: Pd-catalyzed highly regioselective olefin isomerization–hydrocarboxylation with formic acid: a facile approach to synthesize linear carboxylic acids from internal olefins

Supplementary files

Article information

Article type
Research Article
Submitted
12 Jan 2025
Accepted
28 Feb 2025
First published
03 Mar 2025

Org. Chem. Front., 2025, Advance Article

Pd-catalyzed highly regioselective olefin isomerization–hydrocarboxylation with formic acid: a facile approach to synthesize linear carboxylic acids from internal olefins

J. Li, T. Shen, Y. Zhuang, F. Wang, T. Zhu, Y. Fu, Y. Min and Y. Shi, Org. Chem. Front., 2025, Advance Article , DOI: 10.1039/D5QO00072F

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