ICCAS OpenIR
Nucleophilic reaction of heterocyclic enamines with nitrile imine 1,3-dipoles
Miao, WS; Xiong, F; Wang, MX; Huang, ZT
2000
Source PublicationSYNTHETIC COMMUNICATIONS
ISSN0039-7911
Volume30Issue:18Pages:3255-3265
AbstractInstead of 1,3-dipolar cycloaddition, the nucleophilic addition reaction proceeded smoothly between heterocyclic enamines 1 or 2 and nitrile imine 1,3-dipoles 3 under mild conditions to yield C-hydrazidoyl-substituted heterocyclic enamines 4-6 as the sole product.
Indexed BySCI ; IC ; CCR
Language英语
WOS IDWOS:000088624100003
PublisherTAYLOR & FRANCIS INC
Citation statistics
Cited Times:3[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.iccas.ac.cn/handle/121111/75756
Collection中国科学院化学研究所
Corresponding AuthorWang, MX
AffiliationChinese Acad Sci, Ctr Mol Sci, Inst Chem, Beijing 100080, Peoples R China
Recommended Citation
GB/T 7714
Miao, WS,Xiong, F,Wang, MX,et al. Nucleophilic reaction of heterocyclic enamines with nitrile imine 1,3-dipoles[J]. SYNTHETIC COMMUNICATIONS,2000,30(18):3255-3265.
APA Miao, WS,Xiong, F,Wang, MX,&Huang, ZT.(2000).Nucleophilic reaction of heterocyclic enamines with nitrile imine 1,3-dipoles.SYNTHETIC COMMUNICATIONS,30(18),3255-3265.
MLA Miao, WS,et al."Nucleophilic reaction of heterocyclic enamines with nitrile imine 1,3-dipoles".SYNTHETIC COMMUNICATIONS 30.18(2000):3255-3265.
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