Decarboxylative Functionalizations of Carboxylic Acids

Decarboxylative functionalization of carboxylic acids is an attractive synthetic transformation because carboxylic acid is a fundamental and easily available functional group. Recently, a number of excellent methods for catalytic decarboxylative functionalizations of aliphatic and aromatic carboxylic acids have been reported with transition metal catalysts. However, many challenges still remain in decarboxylative functionalization, such as developing the reaction under metal-free conditions, reactions with tertiary carboxylic acids, and catalytic enantioselective reactions. β-Oxoacids are known to undergo decarboxylation under mild reaction conditions. In the last few years, our research group have studied on the development of novel decarboxylative functionalizations of β-oxoacids and their analogues, especially focusing on reactions with tertiary carboxylic acids under organocatalytic or catalyst free conditions. This article describes our recent research progress on the decarboxylative functionalization of aliphatic carboxylic acids.

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Publication Details

Journal
Journal of Synthetic Organic Chemistry Japan
Published
2025-02-01
DOI
https://doi.org/10.5059/yukigoseikyokaishi.83.108
Primary Topic
Fluorine in Organic Chemistry
Type
article
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article

Decarboxylative Functionalizations of Carboxylic Acids

Kazutaka Shibatomi
Journal of Synthetic Organic Chemistry Japan
Fluorine in Organic Chemistry
article

Decarboxylative Functionalizations of Carboxylic Acids

Kazutaka Shibatomi
article en

Abstract

Decarboxylative functionalization of carboxylic acids is an attractive synthetic transformation because carboxylic acid is a fundamental and easily available functional group. Recently, a number of excellent methods for catalytic decarboxylative functionalizations of aliphatic and aromatic carboxylic acids have been reported with transition metal catalysts. However, many challenges still remain in decarboxylative functionalization, such as developing the reaction under metal-free conditions, reactions with tertiary carboxylic acids, and catalytic enantioselective reactions. β-Oxoacids are known to undergo decarboxylation under mild reaction conditions. In the last few years, our research group have studied on the development of novel decarboxylative functionalizations of β-oxoacids and their analogues, especially focusing on reactions with tertiary carboxylic acids under organocatalytic or catalyst free conditions. This article describes our recent research progress on the decarboxylative functionalization of aliphatic carboxylic acids.

Journal of Synthetic Organic Chemistry JapanVol. 83(2)
Toyohashi University of Technology (JP)
Openalex Percentile: Top 98%
Fluorine in Organic Chemistry
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