LICP OpenIR  > 羰基合成与选择氧化国家重点实验室(OSSO)
N-Heterocyclic carbene catalyzed intramolecular nucleophilic addition of carbonyl anion equivalents to enol ethers
Department羰基合成与选择氧化国家重点实验室
He JM(何金梅); Tang SC(唐寿初); Liu J(刘剑); Su YP(苏瀛鹏); Pan XF(潘鑫复); She XG(厍学功)
2008
Source PublicationTetrahedron
ISSN0040-4020
Volume64Pages:8797-8800
AbstractThe intramolecular nucleophilic addition reaction of acyl anion equivalents to enol ethers is described, which was catalyzed by N-heterocyclic carbenes generated in situ from readily available thiazolium salt. In this transformation, benzofuranones were obtained in excellent yield. In combination with our previous work, the precise mechanistic elucidation for the formation of benzofuranones has been further investigated. A labeling experiment implied that the transformation proceeds through a nucleophilic addition mechanism.
Subject Area物理化学
Funding Organizationthe Special Doctorial Program Funds of the Ministry of Education of China (20040730008);NSFC (QT program, No. 20572037);NCET-05-0879;the key grant project of Chinese ministry of Education (No. 105169);and Gansu Science Foundation (3ZS051-A25-004)
Indexed BySCI
Language英语
Citation statistics
Cited Times:65[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.licp.cn/handle/362003/1914
Collection羰基合成与选择氧化国家重点实验室(OSSO)
Corresponding AuthorShe XG(厍学功)
Recommended Citation
GB/T 7714
He JM,Tang SC,Liu J,et al. N-Heterocyclic carbene catalyzed intramolecular nucleophilic addition of carbonyl anion equivalents to enol ethers[J]. Tetrahedron,2008,64:8797-8800.
APA 何金梅,唐寿初,刘剑,苏瀛鹏,潘鑫复,&厍学功.(2008).N-Heterocyclic carbene catalyzed intramolecular nucleophilic addition of carbonyl anion equivalents to enol ethers.Tetrahedron,64,8797-8800.
MLA 何金梅,et al."N-Heterocyclic carbene catalyzed intramolecular nucleophilic addition of carbonyl anion equivalents to enol ethers".Tetrahedron 64(2008):8797-8800.
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