國家衛生研究院 NHRI:Item 3990099045/16290
English  |  正體中文  |  简体中文  |  全文笔数/总笔数 : 12189/12972 (94%)
造访人次 : 973704      在线人数 : 1000
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/3990099045/16290


    题名: Alkoxylation of ketone mediated by N-heterocyclic carbene borane and sulfuric acid in alcohol
    作者: Tanpure, SD;Chang, PW;Ueng, SH
    贡献者: Institute of Biotechnology and Pharmaceutical Research
    摘要: In this study, a novel method for the alkoxylation of ketones has been developed, employing sulfuric acid and N-heterocyclic carbene boranes (NHC−boranes). The ketones are reduced using NHC−borane (diMe-Imd-BH3) and subsequently alkoxylate with sulfuric acid in alcohol solvents. Due to the stability of NHC−borane in the presence of both moisture and air, this reaction emerges as an effective and accessible approach for organic synthesis.
    日期: 2024-09-27
    關聯: Asian Journal of Organic Chemistry. 2024 Sep 27;Article in Press.
    Link to: http://dx.doi.org/10.1002/ajoc.202400436
    JIF/Ranking 2023: http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=NHRI&SrcApp=NHRI_IR&KeyISSN=2193-5815&DestApp=IC2JCR
    Cited Times(WOS): https://www.webofscience.com/wos/woscc/full-record/WOS:001357602400001
    Cited Times(Scopus): https://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85208494405
    显示于类别:[翁紹華] 期刊論文

    文件中的档案:

    档案 大小格式浏览次数
    SCP85208494405.pdf3768KbAdobe PDF6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