Direct Amidation from Alcohols and Amines through a Tandem Oxidation Process Catalyzed by Heterogeneous-Polymer-Incarcerated Gold Nanoparticles under Aerobic Conditions

被引:38
|
作者
Soule, Jean-Francois [1 ]
Miyamura, Hiroyuki [1 ]
Kobayashi, Shu [1 ]
机构
[1] Univ Tokyo, Sch Sci, Dept Chem, Bunkyo Ku, Tokyo 1130033, Japan
基金
日本学术振兴会; 日本科学技术振兴机构;
关键词
alcohols; amides; heterogeneous catalysis; nanoparticles; oxidation; DEHYDROGENATIVE AMIDE SYNTHESIS; SUPPORTED GOLD; MOLECULAR-OXYGEN; CARBONYLATION REACTIONS; NANOCLUSTER CATALYSTS; ATMOSPHERIC-PRESSURE; EFFICIENT SYNTHESIS; N-FORMYLATION; THIO ACIDS; ALDEHYDES;
D O I
10.1002/asia.201300733
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We describe herein a highly elegant and suitable synthesis of amide products from alcohols and amines through a tandem oxidation process that uses molecular oxygen as a terminal oxidant. Carbon-black-stabilized polymer-incarcerated gold (PICB-Au) or gold/cobalt (PICB-Au/Co) nanoparticles were employed as an efficient heterogeneous catalyst depending on alcohol reactivity and generated only water as the major co-product of the reaction. A wide scope of substrate applicability was shown with 42 examples. The catalysts could be recovered and reused without loss of activity by using a simple operation.
引用
收藏
页码:2614 / 2626
页数:13
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