Metal-Ligand Cooperation in the Catalytic Dehydrogenative Coupling (DHC) of Polyalcohols to Carboxylic Acid Derivatives

被引:49
作者
Trincado, Monica [1 ]
Kuehlein, Klaus [1 ]
Gruetzmacher, Hansjoerg [1 ]
机构
[1] ETH Honggerberg, Dept Chem & Appl Biosci, CH-8093 Zurich, Switzerland
基金
瑞士国家科学基金会;
关键词
biomass; cooperative effects; ligand effects; polyols; rhodium; sustainable chemistry; transfer hydrogenation; N-HETEROCYCLIC CARBENE; HYDROGEN-TRANSFER REACTIONS; OPPENAUER-TYPE OXIDATION; DIRECT AMIDE SYNTHESIS; SELECTIVE OXIDATION; RUTHENIUM COMPLEXES; SECONDARY ALCOHOLS; BORROWING HYDROGEN; RHODIUM(I) AMIDES; AMINO-ALCOHOLS;
D O I
10.1002/chem.201101084
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Several polyols, which are easily available from sugars through biochemical conversion or hydrogenolytic cleavage, are directly converted into carboxylic acids and amides. This efficient dehydrogenative coupling process, catalyzed by a rhodium(I) diolefin amido complex, is an attractive approach for the production of organic fine chemicals from renewable resources. This method tolerates the presence of several hydroxy groups and can be extended to the direct synthesis of lactams from the corresponding amino alcohols under mild conditions.
引用
收藏
页码:11905 / 11913
页数:9
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