中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Enantioselective iodolactonization catalyzed by chiral quaternary ammonium salts derived from cinchonidine

文献类型:期刊论文

作者Wang, M; Gao, LX; Mai, WP; Xia, AX; Wang, F; Zhang, SB
刊名JOURNAL OF ORGANIC CHEMISTRY
出版日期2004-04-16
卷号69期号:8页码:2874-2876
ISSN号0022-3263
DOI10.1021/jo035719e
英文摘要Chiral quaternary ammonium salts derived from cinchonidine have been applied to catalyze the stereoselective iodolactonizations of trans-5-aryl-4-pentenoic acids leading to a mixture of two regioselectively iodolactonized products with fair to excellent yield (37-98%) and moderate enantioselectivity (exo = 42.0% ee, endo = 31.0% ee) under mild conditions. This work is the first example of asymmetric iodolactonization reaction in the presence of less than a stoichiometric amount of chiral reagent.
语种英语
WOS记录号WOS:000220752500035
出版者AMER CHEMICAL SOC
源URL[http://ir.iccas.ac.cn/handle/121111/81587]  
专题中国科学院化学研究所
通讯作者Gao, LX
作者单位Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Polymer Phys & Chem, Changchun 130022, Peoples R China
推荐引用方式
GB/T 7714
Wang, M,Gao, LX,Mai, WP,et al. Enantioselective iodolactonization catalyzed by chiral quaternary ammonium salts derived from cinchonidine[J]. JOURNAL OF ORGANIC CHEMISTRY,2004,69(8):2874-2876.
APA Wang, M,Gao, LX,Mai, WP,Xia, AX,Wang, F,&Zhang, SB.(2004).Enantioselective iodolactonization catalyzed by chiral quaternary ammonium salts derived from cinchonidine.JOURNAL OF ORGANIC CHEMISTRY,69(8),2874-2876.
MLA Wang, M,et al."Enantioselective iodolactonization catalyzed by chiral quaternary ammonium salts derived from cinchonidine".JOURNAL OF ORGANIC CHEMISTRY 69.8(2004):2874-2876.

入库方式: OAI收割

来源:化学研究所

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