中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Enantioselective aldol reaction of cyclic ketones with aryl aldehydes catalyzed by a cyclohexanediamine derived salt in the presence of water

文献类型:期刊论文

作者Lin JH(林锦鸿) ; Zhang CP(张成潘) ; Xiao JC(肖吉昌)
刊名Green Chem.
出版日期2009
卷号11期号:11页码:1750-1753
ISSN号1463-9262
其他题名1,2-环己二胺类三氟甲磺酸盐在水相中催化的不对称Aldol缩合反应
通讯作者肖吉昌
英文摘要Water was found to be a suitable reaction medium for the direct asymmetric aldol reaction of various cyclic ketones with aryl aldehydes catalyzed by a primary-tertiary diamine-Bronsted acid.
学科主题氟化学
收录类别SCI
原文出处http://dx.doi.org/10.1039/b916583e
语种英语
WOS记录号WOS:000271476500007
公开日期2013-04-11
源URL[http://202.127.28.38/handle/331003/25235]  
专题上海有机化学研究所_中科院有机氟化学重点实验室
推荐引用方式
GB/T 7714
Lin JH,Zhang CP,Xiao JC. Enantioselective aldol reaction of cyclic ketones with aryl aldehydes catalyzed by a cyclohexanediamine derived salt in the presence of water[J]. Green Chem.,2009,11(11):1750-1753.
APA 林锦鸿,张成潘,&肖吉昌.(2009).Enantioselective aldol reaction of cyclic ketones with aryl aldehydes catalyzed by a cyclohexanediamine derived salt in the presence of water.Green Chem.,11(11),1750-1753.
MLA 林锦鸿,et al."Enantioselective aldol reaction of cyclic ketones with aryl aldehydes catalyzed by a cyclohexanediamine derived salt in the presence of water".Green Chem. 11.11(2009):1750-1753.

入库方式: OAI收割

来源:上海有机化学研究所

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