田中恒雄 | Department Of Pharmacy Hyogo College Of Medicine

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概要

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著作論文

Synthetic Studies on Aphidicolane and Stemodane Diterpenes. IV.A Stereoselective Formal Total Synthesis of (±)-Aphidicolin
Synthetic Studies on Aphidicolane and Stemodane Diterpenes. III.An Alternative Stereoselective Access to Aphidicolane-Type B/C/D-Ring System
102(P-59) (±)-Scopadulinの全合成(ポスター発表の部)
131(P-78) 抗腫瘍活性アセトゲニンMosin Bの不斉合成研究(ポスター発表の部)
多官能性化合物2- (N-シアノイミノ) チアゾリジン誘導体の合成化学的活用
50(P10) Macrocarpal類の不斉合成研究(ポスター発表の部)
Synthetic Studies on Aphidicolane and Stemodane Diterpenes. V. A Facile Formal Total Synthesis of (±)-Aphidicolin via a Lewis Acid-Mediated Stereoselective Spiroannelation
Lewis Acid-Mediated Stereoselective Spiroannelation : A Facile Access to Aphidicolane and Stemodane B/C/D Ring Systems
P-18 (+)-Perhydrohistrionicotoxinの合成(ポスター発表の部)
Synthetic Studies on Aromadendrane-Type Compounds. II.Stereoselective Synthesis of (+)-1,2-Didehydroaromadendrane
93(P-22) 抗腫瘍活性アセトゲニン類の系統的不斉合成法の開発 : Murisolinの不斉合成への応用(ポスター発表の部)
Asymmetric Desymmetrization of Prochiral 1,3-Diols via Diastereoselective C-O Bond Fission of Bicyclic Acetal Using a Chiral Sulfoxide as a Chiral Auxiliary
Factors Affecting the Dissolution Rate of Sulpiride from Tablets Coated with Polyvinylacetal Diethylaminoacetate, a Gastric-Fluid-Soluble Polymer. II. Effect of Mechanical Destructive Force and Film Coating Strength in the Gastrointestinal Tract
Potent NK_1 Receptor Antagonists : Synthesis and Antagonistic Activity of Various Heterocycles with an N-[3,5-Bis(trifluoromethyl)benzyl]-N-methylcarbamoyl Substituent
Characterization of the CYP2C8 Active Site by Homology Modeling
Characterization of the CYP3A4 Active Site by Homology Modeling
1,6-Asymmetric Induction by Reductive Acetal Cleavage of a Bicyclic Acetal Using a Sulfinyl Chiral Auxiliary
1,6-Asymmetric Induction Utilizing Asymmetric Desymmetrization by Diastereoselective C-O Bond Fission of the 4-Substituted Bicyclic Acetal : Application to a Synthesis of (-)-Frontalin
Development of Cellulose Derivatives as Novel Enteric Coating Agents Soluble at pH 3.5-4.5 and Higher
Asymmetric Synthesis of β-Hydroxy Acid via Stereoselective Dirhodium (II)-Catalyzed C-H Insertion of α-Alkoxydiazoketone

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