ICCAS OpenIR
Asymmetric organocatalytic N-nitroso-aldol reaction of oxindoles
Zhang, Tao; Cheng, Liang; Liu, Li; Wang, Dong; Chen, Yong-Jun
2010-12-08
Source PublicationTETRAHEDRON-ASYMMETRY
ISSN0957-4166
Volume21Issue:23Pages:2800-2806
AbstractAn organocatalytic enantioselective N-nitroso-aldol reaction of 2-oxindoles promoted by a cinchona alkaloid catalyst has been developed. The reaction shows exclusively N-selectivity, affording corresponding products with good to excellent yields (up to 100%) and moderate enantioselectivity. The regioselectivity of nitroso-aldol reaction being controlled by different cinchona catalysts was also observed. (C) 2010 Elsevier Ltd. All rights reserved.
DOI10.1016/j.tetasy.2010.11.002
Indexed BySCI ; IC ; CCR
Language英语
WOS IDWOS:000286862600008
PublisherPERGAMON-ELSEVIER SCIENCE LTD
Citation statistics
Cited Times:47[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.iccas.ac.cn/handle/121111/70628
Collection中国科学院化学研究所
Corresponding AuthorLiu, Li
AffiliationChinese Acad Sci, Inst Chem, CAS Key Lab Mol Recognit & Funct, BNLMS, Beijing 100190, Peoples R China
Recommended Citation
GB/T 7714
Zhang, Tao,Cheng, Liang,Liu, Li,et al. Asymmetric organocatalytic N-nitroso-aldol reaction of oxindoles[J]. TETRAHEDRON-ASYMMETRY,2010,21(23):2800-2806.
APA Zhang, Tao,Cheng, Liang,Liu, Li,Wang, Dong,&Chen, Yong-Jun.(2010).Asymmetric organocatalytic N-nitroso-aldol reaction of oxindoles.TETRAHEDRON-ASYMMETRY,21(23),2800-2806.
MLA Zhang, Tao,et al."Asymmetric organocatalytic N-nitroso-aldol reaction of oxindoles".TETRAHEDRON-ASYMMETRY 21.23(2010):2800-2806.
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