Chia Nan University of Pharmacy & Science Institutional Repository:Item 310902800/21719
English  |  正體中文  |  简体中文  |  Items with full text/Total items : 18034/20233 (89%)
Visitors : 23736278      Online Users : 788
RC Version 7.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
Scope Tips:
  • please add "double quotation mark" for query phrases to get precise results
  • please goto advance search for comprehansive author search
  • Adv. Search
    HomeLoginUploadHelpAboutAdminister Goto mobile version
    Please use this identifier to cite or link to this item: https://ir.cnu.edu.tw/handle/310902800/21719


    Title: Palladium-catalyzed 1,2-addition of organic halides and terminal alkynes to 7-oxabenzonorbornadiene;an efficient route to polyaromatic hydrocarbons
    Authors: Chun-Jung Kuo
    Shu-Jin Cheng
    Shu-Ting Chang
    Charng-Hsing Liu
    Contributors: 醫藥化學系
    Keywords: Multicomponent reactions
    Palla�dium
    Oxabenzonorbornadiene
    Alkynes
    Date: 2008-12
    Issue Date: 2009-10-13 09:09:26 (UTC+8)
    Abstract: A three-component coupling reaction of organic halides with oxabicyclic alkenes and terminal alkynes was catalyzed by a palladium complex and a phase-transfer agent in the presence of aqueous NaOH. The reaction gave a series of 5,6-disubstituated 7-oxabenzonorbornene derivatives in good yields. The disubstituted products from oxabenzonorbornadiene can be readily converted into polyaromatic hydrocarbons by a Lewis acid mediated deoxyaromatization reaction.
    Relation: European Journal of Organic Chemistry 2008(3):p.485 - 491
    Appears in Collections:[Dept. of Food & Drug Industry and Inspective Technology] Periodical Articles

    Files in This Item:

    File SizeFormat
    0KbUnknown2234View/Open


    All items in CNU IR are protected by copyright, with all rights reserved.


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