LICP OpenIR  > 羰基合成与选择氧化国家重点实验室(OSSO)
Ring-opening reactions of 2-aryl-3, 4-dihydropyrans with nucleophiles
Department羰基合成与选择氧化国家重点实验室
Li MH(李明浩); Tang CH(唐从辉); Yang J(杨杰); Gu YL(顾彦龙)
2011
Source PublicationChem. Commun.
ISSN1359-7345
Volume47Pages:4529-4531
AbstractRing-opening reactions of 2-aryl-3, 4-dihydropyrans with nucleophiles were reported for the first time. A possible mechanism was also proposed. Finally, this method was used in the synthesis of a novel tetrahydrocarbazole derivative that possesses a biologically active skeleton.
Subject Area物理化学
Funding OrganizationNational Natural Science Foundation of China (20903042);the Program for new Century Excellent Talents in the University of China (NCET-10-0383);Specialized Research Fund for the Doctoral Program of Higher Education (20090142120081)
Indexed BySCI
Language英语
Citation statistics
Cited Times:31[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.licp.cn/handle/362003/363
Collection羰基合成与选择氧化国家重点实验室(OSSO)
Corresponding AuthorGu YL(顾彦龙)
Recommended Citation
GB/T 7714
Li MH,Tang CH,Yang J,et al. Ring-opening reactions of 2-aryl-3, 4-dihydropyrans with nucleophiles[J]. Chem. Commun.,2011,47:4529-4531.
APA 李明浩,唐从辉,杨杰,&顾彦龙.(2011).Ring-opening reactions of 2-aryl-3, 4-dihydropyrans with nucleophiles.Chem. Commun.,47,4529-4531.
MLA 李明浩,et al."Ring-opening reactions of 2-aryl-3, 4-dihydropyrans with nucleophiles".Chem. Commun. 47(2011):4529-4531.
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