中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Enantioselective Synthesis of Four Natural Homoisoflavonoids

文献类型:期刊论文

作者Yu YC(喻艳超)1; Zhu SJ(朱时俊)1; Lu XW(陆晓伟)1; Wu YK(伍贻康)1; Liu B(刘波)1
刊名Eur. J. Org. Chem.
出版日期2015
期号22页码:4964-4972
其他题名四种天然高异黄酮的对映体选择性合成
通讯作者伍贻康 ; 刘波
英文摘要Four naturally occurring sappanin-type homoisoflavonoids were synthesized in optically active form with the stereogenic centers of predefined absolute configuration constructed by using Evans' asymmetric aldol reaction. Analysis of the synthesized compounds not only confirmed the previously assigned planar structures but also was used to determine the absolute configurations of the natural products. Errors in previously reported NMR signals/solvents are also revealed.
学科主题生命有机化学
收录类别SCI
原文出处http://dx.doi.org/10.1002/ejoc.201500579
语种英语
WOS记录号WOS:000358370700021
源URL[http://ir.sioc.ac.cn/handle/331003/39512]  
专题上海有机化学研究所_生命有机化学国家重点实验室
作者单位1.哈尔宾理工大学
2.中科院上海有机化学研究所, 生命有机化学国家重点实验室
推荐引用方式
GB/T 7714
Yu YC,Zhu SJ,Lu XW,et al. Enantioselective Synthesis of Four Natural Homoisoflavonoids[J]. Eur. J. Org. Chem.,2015(22):4964-4972.
APA 喻艳超,朱时俊,陆晓伟,伍贻康,&刘波.(2015).Enantioselective Synthesis of Four Natural Homoisoflavonoids.Eur. J. Org. Chem.(22),4964-4972.
MLA 喻艳超,et al."Enantioselective Synthesis of Four Natural Homoisoflavonoids".Eur. J. Org. Chem. .22(2015):4964-4972.

入库方式: OAI收割

来源:上海有机化学研究所

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