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	An Effective Method for the Synthesis of 1,3-Dihydro-2H-indazoles via N-N Bond Formation
	Zhang, Xiaoke1,2,3; Pan, Yang2,3; Liang, Peng2,3; Ma, Xiaofeng2,3; Jiao, Wei3; Shao, Huawu3
刊名	ADVANCED SYNTHESIS & CATALYSIS
	2019
卷号	361期号:24页码:5552-5557
关键词	bifunctional amino reagents N1 synthon annulation indazole
ISSN号	1615-4150
DOI	10.1002/adsc.201901331
文献子类	Article
英文摘要	The [4+1] cycloaddition reaction of bifunctional amino reagents has been achieved with in situ formed aza-ortho-quinone methides. Specifically, N-(tosyloxy)carbamates were used as an N1 synthon and bifunctional amino reagents for this transformation, which provides a metal-free, catalyst-free, and oxidant-free strategy to form nitrogen-nitrogen bonds.
学科主题	Organic Chemistry/polymer Science
URL标识	查看原文
WOS关键词	O-QUINONE METHIDES ; ASYMMETRIC-SYNTHESIS ; METAL-FREE ; 1,2-CYCLOPROPANATED SUGARS ; ENANTIOSELECTIVE SYNTHESIS ; ACTIVATION STRATEGY ; 3+2 CYCLOADDITION ; ARYLSULFONAMIDES ; 1,2,3-TRIAZOLES ; CONSTRUCTION
WOS研究方向	Chemistry
语种	英语
出版者	WILEY-V C H VERLAG GMBH
WOS记录号	WOS:000496014200001
内容类型	期刊论文
源URL	[http://210.75.237.14/handle/351003/30918]
专题	国家天然药物工程技术研究中心_天然产物研究
作者单位	1.Univ Chinese Acad Sci, Beijing, Peoples R China 2.Zunyi Med Univ, Zunyi 563006, Guizhou, Peoples R China; 3.Chinese Acad Sci, Nat Prod Res Ctr, Chengdu Inst Biol, Chengdu, Peoples R China;
推荐引用方式 GB/T 7714	Zhang, Xiaoke,Pan, Yang,Liang, Peng,et al. An Effective Method for the Synthesis of 1,3-Dihydro-2H-indazoles via N-N Bond Formation[J]. ADVANCED SYNTHESIS & CATALYSIS,2019,361(24):5552-5557.
APA	Zhang, Xiaoke,Pan, Yang,Liang, Peng,Ma, Xiaofeng,Jiao, Wei,&Shao, Huawu.(2019).An Effective Method for the Synthesis of 1,3-Dihydro-2H-indazoles via N-N Bond Formation.ADVANCED SYNTHESIS & CATALYSIS,361(24),5552-5557.
MLA	Zhang, Xiaoke,et al."An Effective Method for the Synthesis of 1,3-Dihydro-2H-indazoles via N-N Bond Formation".ADVANCED SYNTHESIS & CATALYSIS 361.24(2019):5552-5557.

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