Acceptorless Dehydrogenation of Alcohols Catalyzed by CuI N-Heterocycle Thiolate Complexes

被引:37
|
作者
Tan, Da-Wei [1 ]
Li, Hong-Xi [1 ,2 ]
Zhang, Meng-Juan [1 ]
Yao, Jian-Lin [1 ]
Lang, Jian-Ping [1 ,3 ]
机构
[1] Soochow Univ, Coll Chem Chem Engn & Mat Sci, State & Local Joint Engn Lab Novel Funct Polymer, Suzhou 215123, Peoples R China
[2] Soochow Univ, Appl Technol Coll, Suzhou 215325, Peoples R China
[3] Chinese Acad Sci, Shanghai Inst Organ Chem, State Key Lab Organometall Chem, Shanghai 200032, Peoples R China
基金
中国国家自然科学基金;
关键词
alcohols; cluster compounds; copper; dehydrogenation; heterocycles; OXIDANT-FREE DEHYDROGENATION; ASYMMETRIC CONJUGATE ADDITION; AEROBIC OXIDATION CATALYSIS; SECONDARY BENZYLIC ALCOHOLS; PRIMARY ALIPHATIC-ALCOHOLS; SUPPORTED COPPER CATALYST; HETEROGENEOUS CATALYSIS; TRANSFER HYDROGENATION; RUTHENIUM CATALYSTS; BORROWING HYDROGEN;
D O I
10.1002/cctc.201601459
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Cu-I N-heterocycle thiolate clusters efficiently catalyze the acceptorless dehydrogenation of alcohols at 70 degrees C. A variety of secondary/primary benzylic, allylic, and aliphatic alcohols are dehydrogenated to the corresponding ketones and aldehydes in high yields of isolated product upon release of H-2. This simple catalytic system is involved in the synthesis of imines through the one-pot reaction of alcohols and amines.
引用
收藏
页码:1113 / 1118
页数:6
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