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A novel synthetic approach to the bicyclo[5.3.1]-undecan-11-one framework of vinigrol
Alternative TitleA novel synthetic approach to the bicyclo[5.3.1]-undecan-11-one framework of vinigrol
Wang XL(王现磊)1; Lu YY(卢云宇)1; Wang J(王杰)1; Wang X(王璇)1; Yao HQ(姚和权)1; Lin GQ(林国强)1; Sun BF(孙炳峰)1
2014
Source PublicationOrg. Biomol. Chem.
Volume12Issue:22Pages:3562-3566
AbstractThe first synthetic attempt commencing from an eight-membered ring to approach the [5.3.1] bicyclic core of vinigrol has demonstrated the feasibility of using the conformational bias of the cyclooctane-ring system to realize highly diastereoselective reactions. The synthetic potential of the newly disclosed access to in/out isomerism may stimulate broader interests.
Subject Area天然产物有机化学
DOI10.1039/c4ob00046c
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Indexed BySCI
Language英语
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Document Type期刊论文
Identifierhttp://ir.sioc.ac.cn/handle/331003/38982
Collection中科院天然产物有机化学重点实验室
Corresponding AuthorSun BF(孙炳峰)
Affiliation1.中科院上海有机化学研究所
2.中国药科大学
Recommended Citation
GB/T 7714
Wang XL,Lu YY,Wang J,et al. A novel synthetic approach to the bicyclo[5.3.1]-undecan-11-one framework of vinigrol[J]. Org. Biomol. Chem.,2014,12(22):3562-3566.
APA 王现磊.,卢云宇.,王杰.,王璇.,姚和权.,...&孙炳峰.(2014).A novel synthetic approach to the bicyclo[5.3.1]-undecan-11-one framework of vinigrol.Org. Biomol. Chem.,12(22),3562-3566.
MLA 王现磊,et al."A novel synthetic approach to the bicyclo[5.3.1]-undecan-11-one framework of vinigrol".Org. Biomol. Chem. 12.22(2014):3562-3566.
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