Reactions of cyclopropyl aryl ketones with sulfonamides mediated by Zr(OTf)(4): Cascade preparation of 5-aryl-3,4-dihydro-2H-pyrrole
Shi M(施敏) ; Yang YH(杨永华) ; Xu B(胥波)
刊名Synlett
2004
期号9页码:1622-1624
其他题名三氟甲磺酸锆催化的芳香基环丙基酮和磺酰亚胺的串联开环反应研究
通讯作者施敏
英文摘要We found that the Lewis acid Zr(OTf)(4) can effectively promote the ring-opening reaction of cyclopropyl aryl ketones with sulfonamides. By controlling the reaction conditions, we could obtain the ring-opened products 3 and the cyclized products 5 in moderate to good yields. This process provides a novel and efficient route for the synthesis of 5-aryl-3,4-dihydro-2H-pyrrole in the presence of a Lewis acid.
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-2004-829062
语种英语
WOS记录号WOS:000223012000039
公开日期2013-01-09
内容类型期刊论文
源URL[http://202.127.28.38/handle/331003/9910]  
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
Shi M,Yang YH,Xu B. Reactions of cyclopropyl aryl ketones with sulfonamides mediated by Zr(OTf)(4): Cascade preparation of 5-aryl-3,4-dihydro-2H-pyrrole[J]. Synlett,2004(9):1622-1624.
APA Shi M,Yang YH,&Xu B.(2004).Reactions of cyclopropyl aryl ketones with sulfonamides mediated by Zr(OTf)(4): Cascade preparation of 5-aryl-3,4-dihydro-2H-pyrrole.Synlett(9),1622-1624.
MLA Shi M,et al."Reactions of cyclopropyl aryl ketones with sulfonamides mediated by Zr(OTf)(4): Cascade preparation of 5-aryl-3,4-dihydro-2H-pyrrole".Synlett .9(2004):1622-1624.
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