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    Please use this identifier to cite or link to this item: http://ir.nhri.org.tw/handle/3990099045/1252


    Title: Substituent effects on di-pi-methane and aza-di-pi-methane rearrangements of dibenzo[f,h]quinoxalinobarrelenes
    Other Titles: Substituent effects on di-π-methane and aza-di-π-methane rearrangements of dibenzo[f,h]quinoxalinobarrelenes
    Authors: Lin, SY;Hsieh, HP;Peddinti, RK;Liao, CC
    Contributors: Division of Biotechnology and Pharmaceutical Research
    Abstract: The photochemical isomerizations of the title barrelenes providing the corresponding semibullvalenes are described. The modes of competitive di-pi-methane and aza-di-pi-methane rearrangements depend on the substitutions on the heterobarrelenes. (C) 2003 Elsevier Ltd. All rights reserved.
    Keywords: Chemistry, Organic
    Date: 2003-12-01
    Relation: Tetrahedron Letters. 2003 Dec;44(49):8761-8764.
    Link to: http://dx.doi.org/10.1016/j.tetlet.2003.09.200
    JIF/Ranking 2023: http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=NHRI&SrcApp=NHRI_IR&KeyISSN=0040-4039&DestApp=IC2JCR
    Cited Times(WOS): https://www.webofscience.com/wos/woscc/full-record/WOS:000186558000003
    Cited Times(Scopus): http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=0242266553
    Appears in Collections:[謝興邦] 期刊論文

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