N-Heterocyclic Carbene Catalyzed Generation and [4+2] Annulation of Unsubstituted Dienolate - Enantioselective Synthesis of Spirocyclic Oxindolodihydropyranones

doi:10.1002/ejoc.201403395

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	N-Heterocyclic Carbene Catalyzed Generation and [4+2] Annulation of Unsubstituted Dienolate - Enantioselective Synthesis of Spirocyclic Oxindolodihydropyranones
	Cheng, Jin-Tang 1; Chen, Xiang-Yu 1; Gao, Zhong-Hua 1; Ye, Song 1,2
刊名	EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
	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
DOI	10.1002/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
出版者	WILEY-V C H VERLAG GMBH
WOS记录号	WOS:000349391700017
内容类型	期刊论文
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.