中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Highly enantioselective construction of spiro[4h-pyran-3,3 '-oxindoles] through a domino knoevenagel/michael/cyclization sequence catalyzed by cupreine

文献类型:期刊论文

作者Chen, Wen-Bing1,2; Wu, Zhi-Jun2,3; Pei, Qing-Lan1,2; Cun, Lin-Feng1; Zhang, Xiao-Mei1; Yuan, Wei-Cheng1
刊名Organic letters
出版日期2010-07-16
卷号12期号:14页码:3132-3135
ISSN号1523-7060
DOI10.1021/ol1009224
通讯作者Yuan, wei-cheng()
英文摘要The first enantioselective organocatalytic two- and three-component reactions via a domino knoevenagel/michael/cyclization sequence with cupreine as catalyst have been developed. a wide range of optically active spiro[4h-pyran-3,3'-oxindoles] were obtained in excellent yields (up to 99%) with good to excellent enantioselectivities (up to 97%) from simple and readily available starting materials under mild reaction conditions. these heterocyclic spirooxindoles will provide promising candidates for chemical biology and drug discovery.
WOS关键词ANNULATED HETEROCYCLIC-SYSTEMS ; ONE-POT SYNTHESIS ; SPIROCYCLIC OXINDOLES ; CONJUGATE ADDITIONS ; STEREOSELECTIVE-SYNTHESIS ; QUATERNARY STEREOCENTERS ; MULTICOMPONENT REACTIONS ; TERTIARY STEREOCENTERS ; EFFICIENT SYNTHESIS ; CINCHONA ALKALOIDS
WOS研究方向Chemistry
WOS类目Chemistry, Organic
语种英语
WOS记录号WOS:000279569600005
出版者AMER CHEMICAL SOC
URI标识http://www.irgrid.ac.cn/handle/1471x/2409612
专题中国科学院大学
通讯作者Yuan, Wei-Cheng
作者单位1.Chinese Acad Sci, Chengdu Inst Organ Chem, Chengdu 610041, Peoples R China
2.Chinese Acad Sci, Grad Sch, Beijing, Peoples R China
3.Chinese Acad Sci, Chengdu Inst Biol, Chengdu 610041, Peoples R China
推荐引用方式
GB/T 7714
Chen, Wen-Bing,Wu, Zhi-Jun,Pei, Qing-Lan,et al. Highly enantioselective construction of spiro[4h-pyran-3,3 '-oxindoles] through a domino knoevenagel/michael/cyclization sequence catalyzed by cupreine[J]. Organic letters,2010,12(14):3132-3135.
APA Chen, Wen-Bing,Wu, Zhi-Jun,Pei, Qing-Lan,Cun, Lin-Feng,Zhang, Xiao-Mei,&Yuan, Wei-Cheng.(2010).Highly enantioselective construction of spiro[4h-pyran-3,3 '-oxindoles] through a domino knoevenagel/michael/cyclization sequence catalyzed by cupreine.Organic letters,12(14),3132-3135.
MLA Chen, Wen-Bing,et al."Highly enantioselective construction of spiro[4h-pyran-3,3 '-oxindoles] through a domino knoevenagel/michael/cyclization sequence catalyzed by cupreine".Organic letters 12.14(2010):3132-3135.

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来源:中国科学院大学

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