N-Heterocyclic carbene catalyzed intramolecular nucleophilic addition of carbonyl anion equivalents to enol ethers
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)
刊名Tetrahedron
2008
卷号64页码:8797-8800
ISSN号0040-4020
通讯作者厍学功
中文摘要The 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.
学科主题物理化学
收录类别SCI
资助信息the 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)
语种英语
WOS记录号WOS:000258841100029
公开日期2012-11-09
内容类型期刊论文
源URL[http://210.77.64.217/handle/362003/1914]  
专题兰州化学物理研究所_OSSO国家重点实验室
推荐引用方式
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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