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Synthesis of the 6,6,5,7-etracyclic core of daphnilongeranin B
Alternative TitleSynthesis of the 6,6,5,7-etracyclic core of daphnilongeranin B
Xiong XC(熊小春)1; Li Y(郦勇)1; Lu ZY(鲁照永)1; Wan M(万明)1; Deng J(邓军)1; Wu SH(吴淑航)1; Shao HW(邵华武)1; Li A(李昂)1
Source PublicationChem. Commun.
AbstractAn efficient approach toward the synthesis of the 6,6,5,7-tetracyclic core of the daphnilongeranin B, a Daphniphyllum alkaloid, is reported. The bridged 6,6-bicyclic system was constructed using a gold(I) catalysed Conia-ene reaction, while the 5-and 7-membered rings were assembled by two diastereoselective Michael addition reactions, respectively.
Subject Area生命有机化学
Indexed BySCI
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Cited Times:43[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Corresponding AuthorShao HW(邵华武); Li A(李昂)
Recommended Citation
GB/T 7714
Xiong XC,Li Y,Lu ZY,et al. Synthesis of the 6,6,5,7-etracyclic core of daphnilongeranin B[J]. Chem. Commun.,2014,50(40):5294-5297.
APA 熊小春.,郦勇.,鲁照永.,万明.,邓军.,...&李昂.(2014).Synthesis of the 6,6,5,7-etracyclic core of daphnilongeranin B.Chem. Commun.,50(40),5294-5297.
MLA 熊小春,et al."Synthesis of the 6,6,5,7-etracyclic core of daphnilongeranin B".Chem. Commun. 50.40(2014):5294-5297.
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