ICCAS OpenIR
Highly Enantioselective and Organocatalytic alpha-Amination of 2-Oxindoles
Cheng, Liang1; Liu, Li1; Wang, Dong1; Chen, Yong-Jun1
2009-09-03
Source PublicationORGANIC LETTERS
ISSN1523-7060
Volume11Issue:17Pages:3874-3877
AbstractAn effective method for the asymmetric synthesis of 3-amino-2-oxindoles was developed. The tetrasubstituted chiral carbon center was generated by asymmetric amination of N-unprotected 2-oxindoles with azodicarboxylate catalyzed by commercial biscinchona alkaloids In good to excellent yields with high enantioselectivities.
DOI10.1021/ol901405r
Indexed BySCI ; IC ; CCR
Language英语
WOS IDWOS:000269252900022
PublisherAMER CHEMICAL SOC
Citation statistics
Cited Times:166[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.iccas.ac.cn/handle/121111/67756
Collection中国科学院化学研究所
Corresponding AuthorLiu, Li
Affiliation1.Chinese Acad Sci, Inst Chem, CAS Key Lab Mol Recognit & Funct, BNLMS, Beijing 100190, Peoples R China
2.Chinese Acad Sci, Grad Sch, Beijing 100049, Peoples R China
Recommended Citation
GB/T 7714
Cheng, Liang,Liu, Li,Wang, Dong,et al. Highly Enantioselective and Organocatalytic alpha-Amination of 2-Oxindoles[J]. ORGANIC LETTERS,2009,11(17):3874-3877.
APA Cheng, Liang,Liu, Li,Wang, Dong,&Chen, Yong-Jun.(2009).Highly Enantioselective and Organocatalytic alpha-Amination of 2-Oxindoles.ORGANIC LETTERS,11(17),3874-3877.
MLA Cheng, Liang,et al."Highly Enantioselective and Organocatalytic alpha-Amination of 2-Oxindoles".ORGANIC LETTERS 11.17(2009):3874-3877.
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