1,3-Dipolar Cycloaddition Reactions of Vinylidenecyclopropane-Diesters with Aromatic Diazomethanes Generated in Situ

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	1,3-Dipolar Cycloaddition Reactions of Vinylidenecyclopropane-Diesters with Aromatic Diazomethanes Generated in Situ
	Wu L(吴蕾) ; Shi M(施敏)
刊名	J. Org. Chem.
	2010
卷号	75 期号:7 页码:2296-2301
ISSN号	0022-3263
其他题名	亚乙烯基环丙烷和芳基重氮化合物的1,3-环加成反应
英文摘要	1,3-Dipolar cycloaddition reactions of VDCP-diesters with aromatic diazomethanes generated ill situ from the corresponding aromatic aldehydes and tosylhydrazine mediated by base produce pyrazole derivatives in good yields under mild conditions. A plausible reaction mechanism has been proposed on the basis of control experiments along with the discussion Oil the regioselectivity.
学科主题	金属有机化学
收录类别	SCI
原文出处	http://dx.doi.org/10.1021/jo100105k
语种	英语
WOS记录号	WOS:000275884400017
公开日期	2013-01-09
内容类型	期刊论文
源URL	[http://202.127.28.38/handle/331003/10382]
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	Wu L,Shi M. 1,3-Dipolar Cycloaddition Reactions of Vinylidenecyclopropane-Diesters with Aromatic Diazomethanes Generated in Situ[J]. J. Org. Chem.,2010,75(7):2296-2301.
APA	吴蕾,&施敏.(2010).1,3-Dipolar Cycloaddition Reactions of Vinylidenecyclopropane-Diesters with Aromatic Diazomethanes Generated in Situ.J. Org. Chem.,75(7),2296-2301.
MLA	吴蕾,et al."1,3-Dipolar Cycloaddition Reactions of Vinylidenecyclopropane-Diesters with Aromatic Diazomethanes Generated in Situ".J. Org. Chem. 75.7(2010):2296-2301.