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Efficient formal synthesis of the dendrobatid aldaloid, indolizidine(-)-209B
Alternative Titlededrobatid 生物碱indolizidine(-)209B的便利的表观合成
Ma DW(马大为); Pu XT(蒲晓涛); Wang JY(王进义)
Source PublicationTetrahedron-Asymmetry
AbstractCondensation of the β-amino alcohol 7 dervived from an enantiopure β-amino ester with the β-keto ester 8 provides the vinylogous urethane 9, which is cyclized to give the dehydropiperidine 10. Hydrogenation of 10 and subsequent cyclization mediated by Ph^3P/CBr^4 then afforded the bicyclic product 12, a precursor of indolizidine (-)-209B
Subject Area生命有机化学
Indexed BySCI
Document Type期刊论文
Corresponding AuthorMa DW(马大为)
Recommended Citation
GB/T 7714
Ma DW,Pu XT,Wang JY. Efficient formal synthesis of the dendrobatid aldaloid, indolizidine(-)-209B[J]. Tetrahedron-Asymmetry,2002,13(20):2257-2260.
APA 马大为,蒲晓涛,&王进义.(2002).Efficient formal synthesis of the dendrobatid aldaloid, indolizidine(-)-209B.Tetrahedron-Asymmetry,13(20),2257-2260.
MLA 马大为,et al."Efficient formal synthesis of the dendrobatid aldaloid, indolizidine(-)-209B".Tetrahedron-Asymmetry 13.20(2002):2257-2260.
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