Recent Developments of Transition‐Metal‐Catalyzed Cross‐Coupling of Nitriles and Alcohols

Abstract Cross‐coupling of nitriles and alcohols offers an environmentally friendly and atom‐economical method for the synthesis of various valuable compounds. These compounds include α ‐alkylated and α ‐olefinated nitriles, primary amines, imines, N ‐alkylation amines, amides, N ‐heterocycles, δ ‐hydroxynitriles, olefins, etc . Herein, we have reviewed recent developments (from 2013–date) of transition‐metal‐catalyzed cross‐coupling of nitriles and alcohols. A number of transition metal complexes such as noble metals Ru and Ir, as well as base metals Mn, Fe, Co, and Ni are presented. Moreover, different product types, reaction conditions and mechanisms are discussed to understand the reaction and catalyst development.

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Publication Details

Journal
ChemistrySelect
Published
2024-08-22
DOI
https://doi.org/10.1002/slct.202402955
Citations
5
Primary Topic
Asymmetric Hydrogenation and Catalysis
Type
article
Field-Weighted Citation Impact
0.79

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article

Recent Developments of Transition‐Metal‐Catalyzed Cross‐Coupling of Nitriles and Alcohols

Xurui Wei, Ming Huang, Xiuju Cai
5 citations
ChemistrySelect
Asymmetric Hydrogenation and Catalysis
0.79
article

Recent Developments of Transition‐Metal‐Catalyzed Cross‐Coupling of Nitriles and Alcohols

Xurui Wei, Ming Huang, Xiuju Cai
article en
5 citations

Abstract

Abstract Cross‐coupling of nitriles and alcohols offers an environmentally friendly and atom‐economical method for the synthesis of various valuable compounds. These compounds include α ‐alkylated and α ‐olefinated nitriles, primary amines, imines, N ‐alkylation amines, amides, N ‐heterocycles, δ ‐hydroxynitriles, olefins, etc . Herein, we have reviewed recent developments (from 2013–date) of transition‐metal‐catalyzed cross‐coupling of nitriles and alcohols. A number of transition metal complexes such as noble metals Ru and Ir, as well as base metals Mn, Fe, Co, and Ni are presented. Moreover, different product types, reaction conditions and mechanisms are discussed to understand the reaction and catalyst development.

ChemistrySelectVol. 9(32)
Guangdong Pharmaceutical University (CN)
National Natural Science Foundation of China
Life in Land, Responsible consumption and production
Openalex Percentile: Top 33%
Asymmetric Hydrogenation and Catalysis
0.79
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