Stereoselective Synthesis of erythro-Serricornin, (4R, 6R, 7S)-, and (4596R, 75)-4?6-Dimethyl-7-hydroxynonan-3-one9 Stereoisomers of the Sex Pheromone of Cigarette Beetle
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概要
- 論文の詳細を見る
A stereoselective synthesis of erythro-serricornin [(4RS, 6R, 7S)-4, 6-dimethyl-7-hydroxynonan-3-one] was completed starting from L-(+)-tartaric acid. The relative configuration of C(6)-methyl and C(7)-hydroxyl groups in naturally occurring serricornin was threo.
- 社団法人 日本農芸化学会の論文
著者
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Kohno M
Central Research Institute Japan Tobacco Inc.
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NOGUCHI Masao
Central Research Institute, The Japan Tobacco & Salt Public Corporation
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Kohno Masahiro
Central Research Institute Japan Tobacco Inc.
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Mori Kenji
Department of Biochemistry, National Cardiovascular Center Research Institute
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KATO Kunio
Central Research Institute, The Japan Tobacco and Salt Public Corporation
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CHUMAN Tatsuji
Central Research Institute, Japan Tobacco Inc.
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Nomi Hiroko
Department of Agricultural Chemistry, The University of Tokyo
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Noguchi Masao
Central Research Institute The Japan Tobacco & Salt Public Corporation
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Kato Kunio
Central Research Institute The Japan Tobacco & Salt Public Corporation
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Mori Kenji
Department Of Agricultural Chemistry College Of Science And Technology The University Of Tokyo
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