國家衛生研究院 NHRI:Item 3990099045/14308
English  |  正體中文  |  简体中文  |  全文笔数/总笔数 : 12145/12927 (94%)
造访人次 : 852088      在线人数 : 1340
RC Version 6.0 © 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
    主页登入上传说明关于NHRI管理 到手机版


    jsp.display-item.identifier=請使用永久網址來引用或連結此文件: http://ir.nhri.org.tw/handle/3990099045/14308


    题名: Robust synthesis of tetra-boronate esters analogues and the corresponding boronic acids derivatives
    作者: Qiu, SB;Xiao, JH;Chen, PR;Ai, GL;Pan, KL;Chen, JK;Chen, YW;Pan, PS
    贡献者: Institute of Biomedical Engineering and Nanomedicine
    摘要: Organoboron compounds are widely used in catalytic reactions, medicinal chemistry, chemosensors, and polymer applications, because of their low toxicity, high stability, Lewis acidity, chemical versatility, and ability to form covalent bonds with their nucleophilic targets, In this report, we demonstrate how to efficiently assemble tetra boronate-containing compounds at the gram-scale via a one-pot modified microwave-assisted Ugi-4CR reaction. These boronate esters can then be transformed into the corresponding boronic acids under a reliable deprotection method, also reported herein.
    日期: 2022-08-19
    關聯: European Journal of Organic Chemistry. 2022 Aug 19;2022(31):Article number e202200379.
    Link to: http://dx.doi.org/10.1002/ejoc.202200379
    JIF/Ranking 2023: http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=NHRI&SrcApp=NHRI_IR&KeyISSN=1434-193X&DestApp=IC2JCR
    Cited Times(WOS): https://www.webofscience.com/wos/woscc/full-record/WOS:000803498300001
    Cited Times(Scopus): https://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85130996365
    显示于类别:[陳仁焜] 期刊論文

    文件中的档案:

    档案 描述 大小格式浏览次数
    SCP85130996365.pdf7316KbAdobe PDF249检视/开启


    在NHRI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