The transformations of terpene ketones by oxygen. II. The base-catalyzed autoxidation of pulegone and fukinone and their dihydro compounds.
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概要
- 論文の詳細を見る
Upon autoxidation in alkaline media, pulegone and fukinone (<B>2</B>) gave pairs of hydroxy ketones respectively as the major products; also, hydroxyeremophilone was isolated as its acetate from <B>2</B>. On the other hand, their dihydro compounds afforded hydroxy ketones, diosphenols, and acids.
- 公益社団法人 日本化学会の論文
著者
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Naya Keizo
Department of Chemistry, Faculty of Science, Kwansei Gakuin University
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Yo Eiyu
Department of Chemistry, Faculty of Science, Kwansei Gakuin University
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Horinaka Akio
Department of Chemistry, Faculty of Science, Kwansei Gakuin University
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Mori Otoji
Department of Chemistry, Faculty of Science, Kwansei Gakuin University
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- The transformations of terpene ketones by oxygen. I. The autoxidation of fukinone.
- The transformations of terpene ketones by oxygen. II. The base-catalyzed autoxidation of pulegone and fukinone and their dihydro compounds.
- The Structure of Petasitolone, a New Constituent of Petasites japonicus Maxim
- The Structural Elucidation of Sesquiterpene Lactones from Petasites japonicus Maxim
- The Preparation of Fukinane, A New Skeletal Sesquiterpene Hydrocarbon