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Faculty Of Pharmaceutical Sciences Osaka University | 論文
- Asymmetric Synthesis Using Chiral Acetals : Studies on the Nucleophilic Addition of Organometaltics to Chiral α-Keto Acetals in Cyclic Systems(Organic,Chemical)
- Reaction of Silylketenes with Carbanions : Simple Preparation of α-Silylketones Using Organocerium Reagents
- Chemistry of Silylketenes : Simple Preparation of Silylallenes by the Reaction of Silyketenes with Phosphorus Ylides
- Synthetic Anthracyclines : Total Synthesis of D-Ring Pyridine and Pyrazine Analogues of 11-Deoxydaunomycin
- Synthetic Anthracyclines : Regiospecific Total Synthesis so D-Ring Thiophene Analogues of Daunomycin
- Total Synthesis of 11-Deoxyanthracyclines : 4-Demethoxy-11-deoxy-daunomycin : 11-Deoxydaunomycin, and Their Analogues
- An Efficient, Regiospecific Synthesis of 4-Demethoxydaunomycinone and Daunomycinone(Organic,Chemical)
- Synthesis of the Erythrinan Skeleton by Acid-Promoted Cyclization of N-(3-Oxo-1-cyclohexen-1-yl)-N-[2-(3,4-dimethoxyphenyl) ethyl]-α-(methylsulfinyl) acetamide
- 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
- ミクロンサイズのポリ(N-イソプロピルアクリルアミド)ヒドロゲル粒子の作製 : 開始剤の濃度と種類の影響
- ポリ(N-イソプロピルアクリルアミド)/ポリ(エチレングリコール)ジブロック共重合体の性質に及ぼす合成条件の影響
- Chemistry of 2-Methoxy-2,5-cyclohexadienone. V. Photochemical Rearrangement and Oxidation of 2-Methoxy-4-methyl-4-phenyl-2-cyclohexenone and 2-Methoxy-4-methyl-4-phenyl-2,5-eyclohexadienone(Organic,Chemical)
- Synthesis in the Diazasteroid Group. XX. Synthesis of the 5,14-Diazasteroid System(Organic,Chemical)
- Favorskii Reaction of 2-Bromobicyclo[3.3.1]nonan-3-one
- Reaction of Aliphatic Dicarboxylic Acids with Acyl Chlorides in the Presence of Aluminum Chloride
- Chemistry of 2-Methoxy-2,5-cyclohexadienone. IV. Photochemistry of 2-Methoxy-4,4-diphenyl-2,5-cyclohexadienone and 4-Dichloromethyl-2-methoxy-4-methyl-2,5-cyclohexadienone
- Reduction of Vinylogous Thioesters with Lithium Aluminum Hydride. II. Reduction of 2-Methyl-3-phenylthio-5-substituted-2-cyclopentenones
- Reduction of Vinylogous Thioesters with Lithium Aluminum Hydride. I. Reduction of β-Phenylthio-α, β-unsaturated Cyclic Ketones
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