中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Asymmetric synthesis of 3,3,5,5-tetrasubstituted 1,2-dioxolanes: total synthesis of epiplakinic acid F

文献类型:期刊论文

作者Tian XY(田湘寅)1; Han JW(韩建伟)1; Zhao Q(赵琼)1; Huang NZ(黄乃正)1
刊名Org. Biomol. Chem.
出版日期2014
卷号12期号:22页码:3686-3700
其他题名不对称合成3,3,5,5-tetrasubstituted 1,2-dioxolanes: 全合成epiplakinic acid F
通讯作者黄乃正
英文摘要The first enantioselective total synthesis of epiplakinic acid F (1) was achieved through a pivotal step involving a radical-mediated asymmetric peroxidation of vinylcyclopropanes with molecular oxygen to construct highly substituted 1,2-dioxolanes. Subsequent conversions of the chiral 1,2-dioxolanes led to total synthesis of epiplakinic acid F (1) and the confirmation of its absolute configuration. The enantiomer of epiplakinic acid F methyl ester (2) was also prepared.
学科主题金属有机化学
收录类别SCI
原文出处http://dx.doi.org/10.1039/c4ob00448e
语种英语
源URL[http://ir.sioc.ac.cn/handle/331003/39125]  
专题上海有机化学研究所_金属有机化学国家重点实验室
作者单位1.中科院上海有机化学研究所
2.香港中文大学
推荐引用方式
GB/T 7714
Tian XY,Han JW,Zhao Q,et al. Asymmetric synthesis of 3,3,5,5-tetrasubstituted 1,2-dioxolanes: total synthesis of epiplakinic acid F[J]. Org. Biomol. Chem.,2014,12(22):3686-3700.
APA 田湘寅,韩建伟,赵琼,&黄乃正.(2014).Asymmetric synthesis of 3,3,5,5-tetrasubstituted 1,2-dioxolanes: total synthesis of epiplakinic acid F.Org. Biomol. Chem.,12(22),3686-3700.
MLA 田湘寅,et al."Asymmetric synthesis of 3,3,5,5-tetrasubstituted 1,2-dioxolanes: total synthesis of epiplakinic acid F".Org. Biomol. Chem. 12.22(2014):3686-3700.

入库方式: OAI收割

来源:上海有机化学研究所

浏览0
下载0
收藏0
其他版本

除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。