國家衛生研究院 NHRI:Item 3990099045/6879
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    Please use this identifier to cite or link to this item: http://ir.nhri.org.tw/handle/3990099045/6879


    Title: Tandem cyclization of alpha-Cyano alpha-Alkynyl aryl ketones induced by tert-Butyl hydroperoxide and tetrabutylammonium iodide
    Other Titles: Tandem cyclization of α-Cyano α-Alkynyl aryl ketones induced by tert-Butyl hydroperoxide and tetrabutylammonium iodide
    Authors: Wong, YC;Tseng, CT;Kao, TT;Yeh, YC;Shia, KS
    Contributors: Institute of Biotechnology and Pharmaceutical Research
    Abstract: The radical cascade protocol of the alpha-cyano alpha-TMS/aryl-capped alkynyl aryl ketones promoted by tert-butyl hydroperoxide under catalysis with tetrabutylammonium iodide in refluxing benzene has been developed, leading to the construction of a variety of highly functionalized [6,6,5] tricyclic frameworks in an efficient manner.
    Date: 2012-12
    Relation: Organic Letters. 2012 Dec;14(23):6024-6027.
    Link to: http://dx.doi.org/10.1021/ol3028972
    JIF/Ranking 2023: http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=NHRI&SrcApp=NHRI_IR&KeyISSN=1523-7060&DestApp=IC2JCR
    Cited Times(WOS): https://www.webofscience.com/wos/woscc/full-record/WOS:000311926000054
    Cited Times(Scopus): http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84870930753
    Appears in Collections:[Kak-Shan Shia] Periodical Articles

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