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	Synthesis of spiro[pyrazolin-3,3′-oxindoles] and 3-arylcarbonylmethyl substituted ylideneoxindoles by 1,3-dipolar cycloadditions of 3-ylideneoxindoles and in-situ-generated α-diazoketones
	Jiang, Shan; Guo, Hong-Mei; Yao, Sheng; Shi, De-Qing*; Xiao, Wen-Jing
刊名	Journal of Organic Chemistry
	2017
卷号	82期号:19页码:10433-10443
ISSN号	0022-3263
DOI	10.1021/acs.joc.7b01907
URL标识	查看原文
WOS记录号	WOS:000412789000049;EI:20182205258543
内容类型	期刊论文
URI标识	http://www.corc.org.cn/handle/1471x/5155497
专题	华中师范大学
作者单位	1.[Guo, Hong-Mei 2.Yao, Sheng 3.Xiao, Wen-Jing 4.Jiang, Shan 5.Shi, De-Qing] Cent China Normal Univ, Coll Chem, Minist Educ, Key Lab Pesticide & Chem Biol, 152 Luoyu Rd, Wuhan 430079, Hubei, Peoples R China.
推荐引用方式 GB/T 7714	Jiang, Shan,Guo, Hong-Mei,Yao, Sheng,et al. Synthesis of spiro[pyrazolin-3,3′-oxindoles] and 3-arylcarbonylmethyl substituted ylideneoxindoles by 1,3-dipolar cycloadditions of 3-ylideneoxindoles and in-situ-generated α-diazoketones[J]. Journal of Organic Chemistry,2017,82(19):10433-10443.
APA	Jiang, Shan,Guo, Hong-Mei,Yao, Sheng,Shi, De-Qing*,&Xiao, Wen-Jing.(2017).Synthesis of spiro[pyrazolin-3,3′-oxindoles] and 3-arylcarbonylmethyl substituted ylideneoxindoles by 1,3-dipolar cycloadditions of 3-ylideneoxindoles and in-situ-generated α-diazoketones.Journal of Organic Chemistry,82(19),10433-10443.
MLA	Jiang, Shan,et al."Synthesis of spiro[pyrazolin-3,3′-oxindoles] and 3-arylcarbonylmethyl substituted ylideneoxindoles by 1,3-dipolar cycloadditions of 3-ylideneoxindoles and in-situ-generated α-diazoketones".Journal of Organic Chemistry 82.19(2017):10433-10443.

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