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学科主题: 天然产物有机化学
题名: Highly enantioselective synthesis of alpha-trichloromethyldihydropyrans catalyzed by bifunctional organocatalysts
其他题名: 双官能团有机催化剂高对映选择性合成α-三氯甲基二氢吡喃
作者: Wang HF(王海峰) ; Li P(李鹏) ; Cui HF(崔海峰) ; Wang XW(王晓炜) ; Zhang JK(张均康) ; Liu W(刘文) ; Zhao G(赵刚)
通讯作者: 赵刚
刊名: Tetrahedron
发表日期: 2011
卷: 67, 期:10, 页:1774-1780
收录类别: SCI
部门归属: 中科院上海有机化学研究所; 中国科学技术大学
英文摘要: The enantioselective Michael addition of alpha-cyanoketones to alpha,beta-unsaturated trichloromethyl ketones was firstly reported. With a phenylalanine-derived bifunctional piperazine/thiourea catalyst, a series of alpha-trichloromethyldihydropyrans were obtained with up to 95% ee and 99% yield. (C) 2011 Elsevier Ltd. All rights reserved.
语种: 英语
相关网址: 查看原文
WOS记录号: WOS:000288188600004
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内容类型: 期刊论文
URI标识: http://ir.sioc.ac.cn/handle/331003/20811
Appears in Collections:中科院天然产物有机化学重点实验室_期刊论文

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Recommended Citation:
Wang HF,Li P,Cui HF,et al. Highly enantioselective synthesis of alpha-trichloromethyldihydropyrans catalyzed by bifunctional organocatalysts[J]. Tetrahedron,2011,67(10):1774-1780.
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