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    Please use this identifier to cite or link to this item: http://asiair.asia.edu.tw/ir/handle/310904400/17243


    Title: One-pot process to prepare 1,1,2,2-tetrafluoroindane from substituted 2,2-difluorostyrene and sodium chlorodifluoroacetate.
    Authors: 李傳珍;Lee, Chuan-Chen
    Contributors: 保健營養生技學系
    Keywords: Difluorostyrene;Sodium chlorodifluoroacetate;Difluorocarbene;Tetrafluorocyclopropanes;Tetrafluoroindanes
    Date: 2007-01
    Issue Date: 2012-11-26 02:30:28 (UTC+0)
    Abstract: Reaction of 2,2-difluorostyrenes and sodium chlorodifluoroacetate in diglyme solution at 180 °C gave 1-aryl-2,2,3,3-tetrafluorocyclopropane as a primary product. After prolong reaction under the same condition, the 1,1,2,2-tetrafluoroindanes can be isolated as the only product in good yields. All the tetrafluorocyclopropanes and tetrafluoroindanes were well characterized by spectroscopic analyses.
    Relation: TETRAHEDRON; 63(1):Pages 120–125.
    Appears in Collections:[Department of Food Nutrition and Healthy Biotechnology] Journal Article

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