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
卷号69期号:8页码:2874-2876
关键词AUXILIARY PHASE 3 HALOCYCLIZATION AMIDES 5-DISUBSTITUTED-GAMMA-BUTYROLACTONES
ISSN号0022-3263
通讯作者gao lx
中文摘要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.
收录类别SCI
语种英语
WOS记录号WOS:000220752500035
公开日期2010-08-17
源URL[http://202.98.16.49/handle/322003/15139]  
专题长春应用化学研究所_长春应用化学研究所知识产出_期刊论文
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:长春应用化学研究所

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