ICCAS OpenIR
Highly enantioselective synthesis of syn-aldols of cyclohexanones via chiral primary amine catalyzed asymmetric transfer aldol reactions in ionic liquid
Zhou, Pengxin2,3; Luo, Sanzhong1; Cheng, Jin-Pei1,2,3
2011
Source PublicationORGANIC & BIOMOLECULAR CHEMISTRY
ISSN1477-0520
Volume9Issue:6Pages:1784-1790
AbstractChiral primary-tertiary diamine/TfOH was found to catalyze kinetic resolution of racemic syn-aldols of cyclohexanones in ionic liquid effectively, affording the chiral syn-aldols with up to 99: 1 syn/anti and 99% ee.
DOI10.1039/c0ob00682c
Indexed BySCI ; IC ; CCR
Language英语
WOS IDWOS:000287931500016
PublisherROYAL SOC CHEMISTRY
Citation statistics
Cited Times:16[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.iccas.ac.cn/handle/121111/71724
Collection中国科学院化学研究所
Corresponding AuthorLuo, Sanzhong
Affiliation1.Chinese Acad Sci, Inst Chem, CAS Key Lab Mol Recognit & Funct, BNLMS, Beijing 100190, Peoples R China
2.Nankai Univ, Dept Chem, Tianjin 300071, Peoples R China
3.Nankai Univ, State Key Lab Elemental Organ Chem, Tianjin 300071, Peoples R China
Recommended Citation
GB/T 7714
Zhou, Pengxin,Luo, Sanzhong,Cheng, Jin-Pei. Highly enantioselective synthesis of syn-aldols of cyclohexanones via chiral primary amine catalyzed asymmetric transfer aldol reactions in ionic liquid[J]. ORGANIC & BIOMOLECULAR CHEMISTRY,2011,9(6):1784-1790.
APA Zhou, Pengxin,Luo, Sanzhong,&Cheng, Jin-Pei.(2011).Highly enantioselective synthesis of syn-aldols of cyclohexanones via chiral primary amine catalyzed asymmetric transfer aldol reactions in ionic liquid.ORGANIC & BIOMOLECULAR CHEMISTRY,9(6),1784-1790.
MLA Zhou, Pengxin,et al."Highly enantioselective synthesis of syn-aldols of cyclohexanones via chiral primary amine catalyzed asymmetric transfer aldol reactions in ionic liquid".ORGANIC & BIOMOLECULAR CHEMISTRY 9.6(2011):1784-1790.
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