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Enantioselective synthesis of bicyclo[2.2.2]octane-1-carboxylates under metal free conditions
Alternative Title无金属催化下的对映选择性合成双环[2.2.2]辛烷-1-羧酸酯
Li YZ(李英姿)1; Wang J(王杰)1; Sun WB(孙网彬)1; Dan YF(单益凡)1; Sun BF(孙炳峰)1; Lin GQ(林国强)1; Zou JP(邹建平)1
2015
Source PublicationOrg. Chem. Front.
Volume2Issue:3Pages:274-278
AbstractA new tandem reaction was realized that permits rapid access to a wide range of bicyclo[2.2.2]octane-1-carboxylates in good to excellent yields with excellent enantioselectivities under metal free, mild, and operationally simple conditions. An open transition state was deemed operative in this highly enantioselective process mediated by an organic base.
Subtype论文
Subject Area天然产物有机化学
DOI10.1039/c4qo00311j
URL查看原文
Indexed BySCI
Language英语
WOS IDWOS:000364444000014
Citation statistics
Cited Times:3[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.sioc.ac.cn/handle/331003/39811
Collection中科院天然产物有机化学重点实验室
Corresponding AuthorSun BF(孙炳峰); Lin GQ(林国强)
Affiliation1.中科院上海有机化学研究所, 天然产物有机合成化学重点实验室
2.苏州大学
Recommended Citation
GB/T 7714
Li YZ,Wang J,Sun WB,et al. Enantioselective synthesis of bicyclo[2.2.2]octane-1-carboxylates under metal free conditions[J]. Org. Chem. Front.,2015,2(3):274-278.
APA 李英姿.,王杰.,孙网彬.,单益凡.,孙炳峰.,...&邹建平.(2015).Enantioselective synthesis of bicyclo[2.2.2]octane-1-carboxylates under metal free conditions.Org. Chem. Front.,2(3),274-278.
MLA 李英姿,et al."Enantioselective synthesis of bicyclo[2.2.2]octane-1-carboxylates under metal free conditions".Org. Chem. Front. 2.3(2015):274-278.
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