Reagent-controlled enantioselectivity switch for the asymmetric fluorination of beta-ketocarbonyls by chiral primary amine catalysis
You, Yang'en1,2; Zhang, Long1,2,3; Luo, Sanzhong1,2,3
刊名CHEMICAL SCIENCE
2017
卷号8期号:1页码:621-626
英文摘要A reagent-controlled enantioselectivity switch was uncovered in the asymmetric alpha-fluorination of beta-ketocarbonyls by a chiral primary amine catalyst. By a simple swap of fluorination reagents, both enantiomers of the quaternary fluorination adducts could be obtained with good yields and high enantioselectivity. Mechanistic studies disclosed dual H-bonding and electrostatic stereocontrolling modes for the catalysis.
语种英语
内容类型期刊论文
源URL[http://ir.iccas.ac.cn/handle/121111/38013]  
专题化学研究所_分子反应动力学实验室
作者单位1.Chinese Acad Sci, Key Lab Mol Recognit & Funct, Inst Chem, BNLMS, Beijing 100190, Peoples R China
2.Univ Chinese Acad Sci, Beijing 100049, Peoples R China
3.Collaborat Innovat Ctr Chem Sci & Engn, Tianjin 300071, Peoples R China
推荐引用方式
GB/T 7714
You, Yang'en,Zhang, Long,Luo, Sanzhong. Reagent-controlled enantioselectivity switch for the asymmetric fluorination of beta-ketocarbonyls by chiral primary amine catalysis[J]. CHEMICAL SCIENCE,2017,8(1):621-626.
APA You, Yang'en,Zhang, Long,&Luo, Sanzhong.(2017).Reagent-controlled enantioselectivity switch for the asymmetric fluorination of beta-ketocarbonyls by chiral primary amine catalysis.CHEMICAL SCIENCE,8(1),621-626.
MLA You, Yang'en,et al."Reagent-controlled enantioselectivity switch for the asymmetric fluorination of beta-ketocarbonyls by chiral primary amine catalysis".CHEMICAL SCIENCE 8.1(2017):621-626.
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