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Asymmetric Friedel-Crafts Alkylation of Indoles: The Control of Enantio-and Regioselectivity

文献类型:期刊论文

作者Ceng M(曾蜜) ; You SL(游书力)
刊名Synlett
出版日期2010
期号9页码:1289-1301
ISSN号0936-5214
其他题名吲哚的不对称傅克烷基化: 对映体选择性与区域选择性的控制
通讯作者游书力
英文摘要The asymmetric Friedel-Crafts reaction of indoles is a synthetic methodology that enables direct access to the enantiopure indole derivatives. In this review, work mainly carried out by You and his co-workers on the regio- and enantioselective synthesis of indole derivatives will be discussed. Chiral Bronsted acids or iridium complexes promote highly enantioselective Friedel-Crafts reactions of indoles and 4,7-dihydroindoles starting with various electrophilic reagents, such as imines, N-tosyl-substituted amines, beta,gamma-unsaturated a-keto esters, nitro-substituted olefins, aldehydes, and allyl carbonates. These methodologies can be used to readily prepare diverse enantioenriched indoles, such as indol-3-ylmethanamines, indol-2-ylmethanamines, unsymmetrical arylbis(indol-3-yl)methanes, 9-indol-3-ylfluorenes, tetrahydropyrano[3,4-b]indoles, tetrahydro-gamma-carbolines, and tetrahydro-beta-carbolines.
学科主题金属有机化学
收录类别SCI
原文出处http://dx.doi.org/10.1055/s-0029-1219929
语种英语
WOS记录号WOS:000278408800001
公开日期2013-03-04
源URL[http://202.127.28.38/handle/331003/22520]  
专题上海有机化学研究所_金属有机化学国家重点实验室
推荐引用方式
GB/T 7714
Ceng M,You SL. Asymmetric Friedel-Crafts Alkylation of Indoles: The Control of Enantio-and Regioselectivity[J]. Synlett,2010(9):1289-1301.
APA 曾蜜,&游书力.(2010).Asymmetric Friedel-Crafts Alkylation of Indoles: The Control of Enantio-and Regioselectivity.Synlett(9),1289-1301.
MLA 曾蜜,et al."Asymmetric Friedel-Crafts Alkylation of Indoles: The Control of Enantio-and Regioselectivity".Synlett .9(2010):1289-1301.

入库方式: OAI收割

来源:上海有机化学研究所

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