Catalytic Asymmetric Bromination of Unfunctionalized Olefins with H2O as a Nucleophile
Zhang, Xun1; Li, Jing1; Tian, Hua1; Shi, Yian1,2,3
刊名CHEMISTRY-A EUROPEAN JOURNAL
2015-08-10
卷号21期号:33页码:11658-+
关键词bromination cinchona alkaloids enantioselectivity olefins water
英文摘要The dimeric cinchona alkaloid (DHQD)(2)PHAL is used to catalyze an effective asymmetric bromohydroxylation of unfunctionalized olefins with H2O as nucleophile an N-bromobenzamide as a bromine source. A variety of optically active bromohydrins are formed with up to 88%ee.
收录类别SCI
语种英语
公开日期2015-10-27
内容类型期刊论文
源URL[http://ir.iccas.ac.cn/handle/121111/27781]  
专题化学研究所_分子识别与功能实验室
作者单位1.Chinese Acad Sci, Beijing Natl Lab Mol Sci, CAS Key Lab Mol Recognit & Funct, Inst Chem, Beijing 10090, Peoples R China
2.Nanjing Univ, State Key Lab Coordinat Chem, Ctr Multimol Organ Chem, Sch Chem & Chem Engn, Nanjing 210093, Jiangsu, Peoples R China
3.Colorado State Univ, Dept Chem, Ft Collins, CO 80523 USA
推荐引用方式
GB/T 7714
Zhang, Xun,Li, Jing,Tian, Hua,et al. Catalytic Asymmetric Bromination of Unfunctionalized Olefins with H2O as a Nucleophile[J]. CHEMISTRY-A EUROPEAN JOURNAL,2015,21(33):11658-+.
APA Zhang, Xun,Li, Jing,Tian, Hua,&Shi, Yian.(2015).Catalytic Asymmetric Bromination of Unfunctionalized Olefins with H2O as a Nucleophile.CHEMISTRY-A EUROPEAN JOURNAL,21(33),11658-+.
MLA Zhang, Xun,et al."Catalytic Asymmetric Bromination of Unfunctionalized Olefins with H2O as a Nucleophile".CHEMISTRY-A EUROPEAN JOURNAL 21.33(2015):11658-+.
个性服务
查看访问统计
相关权益政策
暂无数据
收藏/分享
所有评论 (0)
暂无评论
 

除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。


©版权所有 ©2017 CSpace - Powered by CSpace