Synthesis of racemic tertiary cyanohydrins

被引:80
作者
Chen, FX [1 ]
Feng, XM [1 ]
机构
[1] Sichuan Univ, Minist Educ, Coll Chem, Key Lab Green Chem & Technol, Chengdu 610064, Peoples R China
关键词
alcohols; catalysis; ketones; nitriles; nucleophilic additions;
D O I
10.1055/s-2005-864831
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The addition of TMS-CN to ketones is catalyzed by homo- and heterogeneous catalysts, which are rationally designed by the line of hydrogen bond activation, dual activation, and the general concept of green chemistry. Especially noteworthy is that those approaches could be readily transferred to enantioselective version of the art. This account describes the development of the catalyst and comparison of the catalytic capacity depending on the nature of the catalyst and structural modifications with mechanism elucidation in appropriate position.
引用
收藏
页码:892 / 899
页数:8
相关论文
共 73 条
[71]   Iodine as novel reagent for the 1,2-addition of trimethylsilyl cyanide to ketones including α,β-unsaturated ketones [J].
Yadav, JS ;
Reddy, BVS ;
Reddy, MS ;
Prasad, AR .
TETRAHEDRON LETTERS, 2002, 43 (52) :9703-9706
[72]  
Yang Y, 1997, SYNLETT, P1379
[73]   Cyanosilylation of ketones catalyzed by quaternary ammonium salt and N-oxide [J].
Zhou, H ;
Chen, FX ;
Qin, B ;
Feng, ZM ;
Zhang, GL .
SYNLETT, 2004, (06) :1077-1079