Alkyl Phosphine Free, Metal-Ligand Cooperative Complex Catalyzed Alcohol Dehydrogenative Coupling Reactions

被引:20
|
作者
Roy, Bivas Chandra [1 ]
Ganguli, Kasturi [1 ]
Samim, Sk. Abdus [1 ]
Kundu, Sabuj [1 ]
机构
[1] IIT Kanpur, Dept Chem, Kanpur 208016, UP, India
关键词
metal-ligand cooperation; bifunctional; acceptorless dehydrogenative coupling; borrowing hydrogen; alcohol; ASYMMETRIC TRANSFER HYDROGENATION; BIFUNCTIONAL IRIDIUM COMPLEX; RUTHENIUM HYDRIDE COMPLEXES; ALPHA-ALKYLATION; BORROWING HYDROGEN; SECONDARY ALCOHOLS; SUSTAINABLE SYNTHESIS; BETA-ALKYLATION; N-HETEROCYCLES; AQUEOUS-MEDIA;
D O I
10.1002/ajoc.202100034
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
In last two decades alcohol has drawn a special attention as a building blocks due to its abundance, low cost and less toxic nature which can be derived from various sustainable resources. By dehydrogenation of alcohol, aldehyde/ketone can be easily accessed which can be further coupled with several nucleophiles for the construction of complex molecules. Among the various strategies, metal-ligand cooperation is a powerful and efficient tool for the utilization of alcohol to synthesize variety of value-added products. Numerous alkyl phosphine based bifunctional complexes are well-known in the literature for the alcohol dehydrogenative coupling reactions. However, the presence of alkyl phosphine moiety and air and moisture sensitive nature of the metal complexes hinder their broad application in catalysis. In this minireview, we highlighted air and moisture stable, metal-ligand cooperative 5d, 4d and 3d metal-based complexes which were effectively utilized to fabricate different value-added compounds by alcohol dehydrogenative coupling reactions.
引用
收藏
页码:1218 / 1232
页数:15
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