LICP OpenIR  > 羰基合成与选择氧化国家重点实验室(OSSO)
Total Synthesis of (-)-Bitungolide F
Department羰基合成与选择氧化国家重点实验室
Su YP(苏瀛鹏); Xu YF(徐艳芬); Han JJ(韩俊杰); Zheng JY(郑计岳); Qi J(齐静); Jiang T(蒋拓); Pan XF(潘鑫复); She XG(厍学功)
2009
Source PublicationJournal of Organic Chemistry
ISSN0022-3263
Volume74Issue:7Pages:2743-2749
AbstractAn efficient total synthesis of (-)-bitungolide F (6) in 17 steps and 20.1% yield is described herein. Key steps involve a Myers asymmetric alkylation to introduce the C6 methyl with proper stereochemistry, a Claisen-like cyclization to construct the R, -unsaturated δ-lactone and a Julia-Kocienski olefination to assemble the conjugated diene moiety.
Subject Area物理化学
Funding Organizationthe NSFC (QT program, 20872054;20732002);NCET-05-0879
Indexed BySCI
Language英语
Citation statistics
Cited Times:26[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.licp.cn/handle/362003/535
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
Su YP,Xu YF,Han JJ,et al. Total Synthesis of (-)-Bitungolide F[J]. Journal of Organic Chemistry,2009,74(7):2743-2749.
APA 苏瀛鹏.,徐艳芬.,韩俊杰.,郑计岳.,齐静.,...&厍学功.(2009).Total Synthesis of (-)-Bitungolide F.Journal of Organic Chemistry,74(7),2743-2749.
MLA 苏瀛鹏,et al."Total Synthesis of (-)-Bitungolide F".Journal of Organic Chemistry 74.7(2009):2743-2749.
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