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    Please use this identifier to cite or link to this item: https://ir.fy.edu.tw:8080/ir/handle/987654321/2287

    Title: Claisen rearrangement/Baylis–Hillman reaction/ring-closing metathesis as bases for the construction of substituted cyanonaphthalenes
    Authors: Po-Yuan Chen;Hsing-Ming Chen;Liang-Yeu Chen;Jing-Yu Tzeng;Jui-Chi Tsai;Ping-Cheng Chi;Sie-Rong Li;Eng-Chi Wang
    Contributors: 輔英科技大學 保健營養系
    Keywords: Claisen rearrangement;Ring-closing metathesis;Cyanonaphthalenes
    Date: 2007-03-01
    Issue Date: 2010-09-26 14:12:26 (UTC+8)
    Abstract: The present paper described how to establish a novel approach for various alkoxycyanonaphthalenes. It was started from isovanillin, and based on the Claisen rearrangement, O-alkylation, the Baylis–Hillman reaction, and ring-closing metathesis in sequence to produce the title compounds in good yield.
    Relation: Tetrahedron 63(13),2824-2828
    Appears in Collections:[保健營養系] 期刊論文

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