ICCAS OpenIR
Organocatalytic kinetic resolution via intramolecular aldol reactions: Enantioselective synthesis of both enantiomers of chiral cyclohexenones
Chen, Liujuan; Luo, Sanzhong; Li, Jiuyuan; Li, Xin; Cheng, Jin-Pei
2010
Source PublicationORGANIC & BIOMOLECULAR CHEMISTRY
ISSN1477-0520
Volume8Issue:11Pages:2627-2632
AbstractKinetic resolution of 6-aryl-2,6-hexanediones was achieved with chiral secondary amine catalyzed intramolecular aldolization. The current kinetic resolution protocol enables the synthesis of both enantiomers of cyclohexenones with moderate to good enantioselectivity.
DOI10.1039/b927343c
Indexed BySCI ; IC ; CCR
Language英语
WOS IDWOS:000277879700022
PublisherROYAL SOC CHEMISTRY
Citation statistics
Cited Times:33[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.iccas.ac.cn/handle/121111/69244
Collection中国科学院化学研究所
Corresponding AuthorLuo, Sanzhong
AffiliationChinese Acad Sci, Inst Chem, BNLMS, Key Lab Mol Recognit & Funct, Beijing 100190, Peoples R China
Recommended Citation
GB/T 7714
Chen, Liujuan,Luo, Sanzhong,Li, Jiuyuan,et al. Organocatalytic kinetic resolution via intramolecular aldol reactions: Enantioselective synthesis of both enantiomers of chiral cyclohexenones[J]. ORGANIC & BIOMOLECULAR CHEMISTRY,2010,8(11):2627-2632.
APA Chen, Liujuan,Luo, Sanzhong,Li, Jiuyuan,Li, Xin,&Cheng, Jin-Pei.(2010).Organocatalytic kinetic resolution via intramolecular aldol reactions: Enantioselective synthesis of both enantiomers of chiral cyclohexenones.ORGANIC & BIOMOLECULAR CHEMISTRY,8(11),2627-2632.
MLA Chen, Liujuan,et al."Organocatalytic kinetic resolution via intramolecular aldol reactions: Enantioselective synthesis of both enantiomers of chiral cyclohexenones".ORGANIC & BIOMOLECULAR CHEMISTRY 8.11(2010):2627-2632.
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