Optically Active 9,10-Dihydro-9,10-etheno and -ethanoanthracenes. I. Syntheses of Optically Active 1,5-Disubstituted-9,10-dihydro-9,10-etheno and -ethanoanthracenes.
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概要
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1,5-Dimethoxycarbonyl-9,10-dihydro-9,10-ethenoanthracene was synthesized by the reaction of 1,5-dimethoxycarbonylanthracene with dichloroethylene followed by dechlorination with zinc-copper couple. Optical resolution of l,5-dicarboxy-9,10-dihydro-9,10-ethenoanthracene prepared from the dimethyl ester could be achieved by strychnine to give optically pure (−)-dicarboxylic acid and (+)-diacid with an optical purity of 87.3%. Catalytic reduction of (−)-dicarboxylic acid afforded (−)-ethano-dicarboxylic acid. Transformation of the carboxyl groups in various substituent groups to give optically active C<SUB>2</SUB>-symmetrical etheno- and ethanoanthracene derivatives belonging to the same series of absolute configuration as that of the starting material is described.
- 公益社団法人 日本化学会の論文
著者
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Ogura Fumio
Department Of Applied Chemistry Faculty Of Engineering Hiroshima University
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Nakagawa Masazumi
Department of Chemistry Faculty of Science Osaka University
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Tatemitsu Hitoshi
Department of Chemistry, Faculty of Science, Osaka University
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