LICP OpenIR  > 羰基合成与选择氧化国家重点实验室(OSSO)
Efficient Asymmetric Total Syntheses of Cryptocarya Triacetate, Cryptocaryolone, and Cryptocaryolone Diacetate
Department羰基合成与选择氧化国家重点实验室
Wang XL(王晓磊); Wang WK(王文宽); Zheng HJ(郑怀基); Su YP(苏瀛鹏); Jiang T(蒋拓); He YP(贺永平); She XG(厍学功)
2009
Source PublicationOrganic Letters
ISSN1523-7060
Volume11Issue:14Pages:3136-3138
AbstractConcise and efficient asymmetric total syntheses of three substituted r-pyrone-type natural products have been accomplished via 7-9 steps from 5b in high overall yields, which involve linchpin coupling, ring-closing metathesis, and a tandem sequence of deacetylation and intramolecular oxa-Michael addition as the key steps.
Subject Area物理化学
Funding Organizationthe NSFC (QT program;20872054;20732002)
Indexed BySCI
Language英语
Citation statistics
Cited Times:40[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.licp.cn/handle/362003/524
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
Wang XL,Wang WK,Zheng HJ,et al. Efficient Asymmetric Total Syntheses of Cryptocarya Triacetate, Cryptocaryolone, and Cryptocaryolone Diacetate[J]. Organic Letters,2009,11(14):3136-3138.
APA 王晓磊.,王文宽.,郑怀基.,苏瀛鹏.,蒋拓.,...&厍学功.(2009).Efficient Asymmetric Total Syntheses of Cryptocarya Triacetate, Cryptocaryolone, and Cryptocaryolone Diacetate.Organic Letters,11(14),3136-3138.
MLA 王晓磊,et al."Efficient Asymmetric Total Syntheses of Cryptocarya Triacetate, Cryptocaryolone, and Cryptocaryolone Diacetate".Organic Letters 11.14(2009):3136-3138.
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