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Diastereoselective Synthesis of 6-Trifluoromethyl-5,6-dihydropyrans via Phosphine-Catalyzed [4+2] Annulation of alpha-Benzylallenoates with Ketones
Wang, Tong; Ye, Song
2010-09-17
Source PublicationORGANIC LETTERS
ISSN1523-7060
Volume12Issue:18Pages:4168-4171
AbstractThe highly diastereoselective synthesis of 6-trifluoromethyl-5,6-dihydropyrans was realized by the phosphine-catalyzed [4 + 2] annulation of ethyl alpha-benzylallenoates and trifluoromethyl ketones.
DOI10.1021/ol101762z
Indexed BySCI ; IC ; CCR
Language英语
WOS IDWOS:000281596800053
PublisherAMER CHEMICAL SOC
Citation statistics
Cited Times:123[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.iccas.ac.cn/handle/121111/70088
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. Diastereoselective Synthesis of 6-Trifluoromethyl-5,6-dihydropyrans via Phosphine-Catalyzed [4+2] Annulation of alpha-Benzylallenoates with Ketones[J]. ORGANIC LETTERS,2010,12(18):4168-4171.
APA Wang, Tong,&Ye, Song.(2010).Diastereoselective Synthesis of 6-Trifluoromethyl-5,6-dihydropyrans via Phosphine-Catalyzed [4+2] Annulation of alpha-Benzylallenoates with Ketones.ORGANIC LETTERS,12(18),4168-4171.
MLA Wang, Tong,et al."Diastereoselective Synthesis of 6-Trifluoromethyl-5,6-dihydropyrans via Phosphine-Catalyzed [4+2] Annulation of alpha-Benzylallenoates with Ketones".ORGANIC LETTERS 12.18(2010):4168-4171.
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