中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
N-Heterocyclic Carbene Catalyzed Generation and [4+2] Annulation of Unsubstituted Dienolate - Enantioselective Synthesis of Spirocyclic Oxindolodihydropyranones

文献类型:期刊论文

作者Cheng, Jin-Tang1; Chen, Xiang-Yu1; Gao, Zhong-Hua1; Ye, Song1,2
刊名EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
出版日期2015-02-01
期号5页码:1047-1053
关键词Asymmetric Catalysis Annulation Spiro Compounds Nitrogen Heterocycles N-heterocyclic Carbenes
ISSN号1434-193X
DOI10.1002/ejoc.201403395
英文摘要The N-heterocyclic carbene catalyzed (NHC-catalyzed) generation of unsubstituted dienolate (butadienolate) and subsequent [4+2] annulation reactions with isatins afford chiral spirocyclic oxindolodihydropyranones in moderate to good yields with moderate to good enantioselectivities.
语种英语
WOS记录号WOS:000349391700017
出版者WILEY-V C H VERLAG GMBH
源URL[http://ir.iccas.ac.cn/handle/121111/53275]  
专题中国科学院化学研究所
通讯作者Ye, Song
作者单位1.Chinese Acad Sci, Inst Chem, CAS Key Lab Mol Recognit & Funct, Beijing Natl Lab Mol Sci, Beijing 100190, Peoples R China
2.Jiangxi Normal Univ, Natl Engn Res Ctr Carbohydrate Synth, Nanchang 330022, Peoples R China
推荐引用方式
GB/T 7714
Cheng, Jin-Tang,Chen, Xiang-Yu,Gao, Zhong-Hua,et al. N-Heterocyclic Carbene Catalyzed Generation and [4+2] Annulation of Unsubstituted Dienolate - Enantioselective Synthesis of Spirocyclic Oxindolodihydropyranones[J]. EUROPEAN JOURNAL OF ORGANIC CHEMISTRY,2015(5):1047-1053.
APA Cheng, Jin-Tang,Chen, Xiang-Yu,Gao, Zhong-Hua,&Ye, Song.(2015).N-Heterocyclic Carbene Catalyzed Generation and [4+2] Annulation of Unsubstituted Dienolate - Enantioselective Synthesis of Spirocyclic Oxindolodihydropyranones.EUROPEAN JOURNAL OF ORGANIC CHEMISTRY(5),1047-1053.
MLA Cheng, Jin-Tang,et al."N-Heterocyclic Carbene Catalyzed Generation and [4+2] Annulation of Unsubstituted Dienolate - Enantioselective Synthesis of Spirocyclic Oxindolodihydropyranones".EUROPEAN JOURNAL OF ORGANIC CHEMISTRY .5(2015):1047-1053.

入库方式: OAI收割

来源: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。