Chia Nan University of Pharmacy & Science Institutional Repository:Item 310902800/30491
English  |  正體中文  |  简体中文  |  全文笔数/总笔数 : 18034/20233 (89%)
造访人次 : 23809346      在线人数 : 633
RC Version 7.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
搜寻范围 查询小技巧:
  • 您可在西文检索词汇前后加上"双引号",以获取较精准的检索结果
  • 若欲以作者姓名搜寻,建议至进阶搜寻限定作者字段,可获得较完整数据
  • 进阶搜寻


    jsp.display-item.identifier=請使用永久網址來引用或連結此文件: https://ir.cnu.edu.tw/handle/310902800/30491


    標題: Catalytic Asymmetric Phenyl Addition of PhTi (OiPr)3 to 2’-Acetonaphthone by Titanium Catalyst of Disulfonamide Ligands
    作者: Chao-Chi Shu
    Han-Mou Gau
    貢獻者: Department of Chemistry, National Chung Hsing University
    日期: 2008-07
    上傳時間: 2017-12-04 15:55:22 (UTC+8)
    摘要: One of the most important challenges in organic synthesis is the enantioselective synthesis of chiral compounds with the quaternary stereocenter. There are a few reports of asymmetric catalytic aryl additions of organometallic reagents to ketones. Recently, we reported asymmetric AlAr3 (THF) additions to ketones catalyzed by titanium cataysts of chiral C2-symmetric ligands. We found that the disulfonamide ligand derived from camphor has shown excellent enantioselectivities in aryl addition to ketones. Thus, in this study, we prepared a series of disulfonamid derivatives of trans-1,2-diaminocyclohexane as ligands in titanium-catalyzed asymmetric phenyl addition reactions. The enantioselective phenylations of 2’-acetonaphthone were successfully performed using the phenyltitanium reagent, magnesium bromide and disulfonamides ligands 1-10, giving the enantiomeric excesses of the product up to 96%.
    關聯: 第五屆海峽化學、生物及材料研討會,起迄日:2008/07/21-2008/07/22,地點:嘉南藥理科技大學
    显示于类别:[藥理學院] 2008第五屆海峽化學、生物及材料研討會

    文件中的档案:

    档案 描述 大小格式浏览次数
    C11.pdf356KbAdobe PDF240检视/开启


    在CNU IR中所有的数据项都受到原著作权保护.

    TAIR相关文章

    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - 回馈