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    Please use this identifier to cite or link to this item: https://tkuir.lib.tku.edu.tw/dspace/handle/987654321/121103


    Title: A case study of the iodine-mediated cyclization of C2'-OH- and C2-OH-chalcones toward the synthesis of flavones:Reinvestigation of the mechanisms
    Authors: Hsin Yen Tsai;Yu-Tzu Huang;Cing-Ling Kuo;Chia-Jou Kuo;Anren Hu;Jih-Jung Chen;Tzenge-Lien Shih
    Date: 2021-02-23
    Issue Date: 2021-08-26 12:11:39 (UTC+8)
    Abstract: Synthesis of flavones from chalcones via the iodine-mediated cyclization required at least one hydroxy group at their C2′-positions. On the contrary, the ring oxidative cyclization from C2-OH-chalcones under the same condition was unusual and reported only once. We evaluated the aforementioned method and found different results. The mechanisms in detail were discussed.
    Relation: Journal of the Chinese Chemical Society 68(7), p.1334-1338
    DOI: 10.1002/jccs.202000482
    Appears in Collections:[Doctoral Program in Applied Science] Journal Article

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