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Phosphine-catalyzed [3+2] cycloaddition of allenoates with trifluoromethylketones: synthesis of dihydrofurans and tetrahydrofurans
Wang, Tong; Ye, Song
2011
Source PublicationORGANIC & BIOMOLECULAR CHEMISTRY
ISSN1477-0520
Volume9Issue:14Pages:5260-5265
AbstractThe triphenylphosphine-catalyzed formal [3 + 2] cycloaddition of allenoates and trifluoromethylketones was realized to give the corresponding dihydrofurans in good yields with excellent gamma-regioselectivities. Hydrogenation of the dihydrofurans gave 2,4,4-trisubstituted tetrahydrofurans in good yields with exclusive cis-selectivities.
DOI10.1039/c1ob05444a
Indexed BySCI ; IC ; CCR
Language英语
WOS IDWOS:000292203800036
PublisherROYAL SOC CHEMISTRY
Citation statistics
Cited Times:50[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.iccas.ac.cn/handle/121111/72126
Collection中国科学院化学研究所
Corresponding AuthorYe, Song
AffiliationChinese Acad Sci, Beijing Natl Lab Mol Sci, CAS Key Lab Mol Recognit & Funct, Inst Chem, Beijing 100190, Peoples R China
Recommended Citation
GB/T 7714
Wang, Tong,Ye, Song. Phosphine-catalyzed [3+2] cycloaddition of allenoates with trifluoromethylketones: synthesis of dihydrofurans and tetrahydrofurans[J]. ORGANIC & BIOMOLECULAR CHEMISTRY,2011,9(14):5260-5265.
APA Wang, Tong,&Ye, Song.(2011).Phosphine-catalyzed [3+2] cycloaddition of allenoates with trifluoromethylketones: synthesis of dihydrofurans and tetrahydrofurans.ORGANIC & BIOMOLECULAR CHEMISTRY,9(14),5260-5265.
MLA Wang, Tong,et al."Phosphine-catalyzed [3+2] cycloaddition of allenoates with trifluoromethylketones: synthesis of dihydrofurans and tetrahydrofurans".ORGANIC & BIOMOLECULAR CHEMISTRY 9.14(2011):5260-5265.
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