Recent Progress in Radical Decarboxylative Functionalizations Enabled by Transition-Metal (Ni, Cu, Fe, Co or Cr) Catalysis

Abstract

Aliphatic carboxylic acids are abundant in natural and synthetic sources and are widely used as connection points in many chemical transformations. Radical decarboxylative functionalization promoted by transition-metal catalysis has achieved great success, enabling carboxylic acids to be easily transformed into a wide variety of products. Herein, we highlight the recent advances made on transition-metal (Ni, Cu, Fe, Co or Cr) catalyzed C–X (X = C, N, H, O, B, or Si) bond formation as well as syntheses of ketones, amino acids, alcohols, ethers and difluoromethyl derivatives via radical decarboxylation of carboxylic acids or their derivatives, including, among others, redox-active esters (RAEs), anhydrides, and diacyl peroxides.

1 Introduction

2 Ni-Catalyzed Decarboxylative Functionalizations

3 Cu-Catalyzed Decarboxylative Functionalizations

4 Fe-Catalyzed Decarboxylative Functionalizations

5 Co- and Cr-Catalyzed Decarboxylative Functionalizations

6 Conclusions

Key words

carboxylic acids - decarboxylative functionalization - transition metals - radicals - redox-active esters (RAEs) - C–X bond formation - catalysis

Publikationsverlauf

Eingereicht: 24. Juni 2020

Angenommen nach Revision: 04. August 2020

Artikel online veröffentlicht:
01. Oktober 2020

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