The Structures of Securinol B and C
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概要
- 論文の詳細を見る
The structures of securinol B and C were determined as Ib and III by conversion of them into viroallosecurinine (II) and allosecurinine (IV), respectively, and from spectral evidences.
- 公益社団法人日本薬学会の論文
- 1970-10-25
著者
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堀井 善一
Faculty Of Pharmaceutical Sciences Josai University
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池田 正澄
Faculty of Pharmaceutical Sciences, Osaka University
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百瀬 雄章
Faculty of Pharmaceutical Sciences, Kinki University
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山内 昌茂
Faculty of Pharmaceutical Sciences, Osaka University
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堀井 善一
Faculty Of Pharmaceutical Sciences Osaka University
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山内 昌茂
Faculty Of Pharmaceutical Sciences Josai University
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百瀬 雄章
Faculty Of Pharmaceutical Sciences Kanazawa University
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- 4 Securinine及びVirosecurinineの全合成
- Total Synthesis of Securinine
- Reaction of Benzo [b] furan and 1-Acylindoles with Iodine Azide
- Synthesis and Some Chemical Transformations of 2-Azidomethylindoles
- Synthesis and Thermolysis of 3-Azidoindolenines
- Favorskii Reaction of 2-Bromobicyclo[3.3.1]nonan-3-one
- Ring Expansion Reaction of 2,2-Dimethyl-2,3-dihydrobenzo [b]-thiophene N-(p-Toluenesulfonyl) sulfilimine
- The Base-induced β-Elimination Reaction of 1,1,1-Trisubstituted Hydrazinium Salts
- 1,6-Dihydro-3 (2H)-pyridinones. II. Synthesis of 2-Azabicyclo [2. 2. 2] octanes by the Reaction of N-Substituted 1,6-Dihydro-3 (2H)-pyridinones with 1,3-Dicarbonyl Compounds