Desymmetrization of cyclohexadienones via D-camphor-derived triazolium salt catalyzed intramolecular Stetter reaction
Jia MQ(贾敏强) ; You SL(游书力)
刊名Chem. Commun.
2012
卷号48期号:51页码:6363-6365
ISSN号1359-7345
其他题名通过D-樟脑衍生的三唑盐催化的分子内Stetter反应实现的环己二酮的去对称化
通讯作者游书力
英文摘要Enantioselective desymmetrization of cyclohexadienones via a D-camphor-derived triazolium salt catalyzed intramolecular Stetter reaction was realized. With 10 mol% of camphor-derived triazolium salt E and 10 mol% of DIEA, various substituted cyclohexadienones proceeded through an intramolecular Stetter reaction, affording tricyclic products in moderate to good yields and excellent ee.
学科主题金属有机化学
收录类别SCI
原文出处http://dx.doi.org/10.1039/c2cc32783j
语种英语
WOS记录号WOS:000304605700011
公开日期2013-08-22
内容类型期刊论文
源URL[http://202.127.28.38/handle/331003/28051]  
专题上海有机化学研究所_金属有机化学国家重点实验室
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Jia MQ,You SL. Desymmetrization of cyclohexadienones via D-camphor-derived triazolium salt catalyzed intramolecular Stetter reaction[J]. Chem. Commun.,2012,48(51):6363-6365.
APA 贾敏强,&游书力.(2012).Desymmetrization of cyclohexadienones via D-camphor-derived triazolium salt catalyzed intramolecular Stetter reaction.Chem. Commun.,48(51),6363-6365.
MLA 贾敏强,et al."Desymmetrization of cyclohexadienones via D-camphor-derived triazolium salt catalyzed intramolecular Stetter reaction".Chem. Commun. 48.51(2012):6363-6365.
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