Tertiary amino thiourea-catalyzed asymmetric cross aldol reaction of aryl methyl ketones with aryl trifluoromethyl ketones

被引:19
作者
Lutete, Leopold Mpaka [1 ]
Miyamoto, Takashi [1 ]
Ikemoto, Tetsuya [1 ]
机构
[1] Sumitomo Chem Co Ltd, Hlth & Crop Sci Res Lab, Nishiyodogawa Ku, 1-21 Utajima 3-Chome, Osaka 5550021, Japan
关键词
Aldol reaction; Thiourea; Bifunctional catalyst; Organocatalysis; Trifluoromethyl ketones; ENANTIOSELECTIVE SYNTHESIS; MICHAEL ADDITION; DUAL ACTIVATION; PROLINE; ORGANOCATALYSIS; MECHANISM;
D O I
10.1016/j.tetlet.2016.02.001
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
An enantioselective aldol reaction of aryl methyl ketones with aryl trifluoromethyl ketones catalyzed by tertiary amino thiourea has been established. Under mild conditions, the corresponding beta-trifluoromethyl-beta-hydroxy ketone products were obtained with up to 89% ee. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1220 / 1223
页数:4
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