Synthetic Studies on Sorigenins. VII. Synthesis of α-Sorigenin Dimethyl Ether (3-Hydroxymethyl-1,6,8-trimethoxy-2-naphthoic Acid γ-Lactone). (2).
スポンサーリンク
概要
- 論文の詳細を見る
The synthesis of α-sorigenin dimethyl ether, 3-hydroxymethyl-1,6,8-trimethoxy-2-naphthoic acid γ-lactone (I), by an unequivocal route as shown in chart is described. The reactions employed for preparing the 1-oxo-3-hydroxymethyl-1,2,3,4-tetrahydro-2-naphthonitrile (VII) from the ethyl 1-oxo-1,2,3,4-tetrahydro-2-naphthoate II via the intermediates, III, IV, and VI, would provide a new method for protecting the keto-group towards lithium aluminum hydride reduction.
- 公益社団法人日本薬学会の論文
- 1963-03-25
著者
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堀井 善一
School of Pharmacy, Osaka University
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田村 恭光
School of Pharmacy, Osaka University
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加多木 豊之
School Of Pharmacy Osaka University
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加多木 豊之
School Of Pharmaceutical Sciences Mukogawa Women 's University
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