中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Organocatalytic kinetic resolution via intramolecular aldol reactions: Enantioselective synthesis of both enantiomers of chiral cyclohexenones

文献类型:期刊论文

作者Chen, Liujuan; Luo, Sanzhong; Li, Jiuyuan; Li, Xin; Cheng, Jin-Pei
刊名ORGANIC & BIOMOLECULAR CHEMISTRY
出版日期2010
卷号8期号:11页码:2627-2632
ISSN号1477-0520
DOI10.1039/b927343c
英文摘要Kinetic 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.
语种英语
WOS记录号WOS:000277879700022
出版者ROYAL SOC CHEMISTRY
源URL[http://ir.iccas.ac.cn/handle/121111/69243]  
专题中国科学院化学研究所
通讯作者Luo, Sanzhong
作者单位Chinese Acad Sci, Inst Chem, BNLMS, Key Lab Mol Recognit & Funct, Beijing 100190, Peoples R China
推荐引用方式
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.

入库方式: OAI收割

来源:化学研究所

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