石墨紀久夫 | Sumitomo Pharmaceuticals Research Center

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著作論文

Benzodiazepines. XI. Further Examination of the Chromic Acid Oxidation of 2-Aminomethylindoles to 2,3-Dihydro-2H-1,4-benzodiazepin-2-ones
Benzodiazepines. X. Oxidation of Tetrahydro-1,4-benzo-diazepine Derivatives
Benzodiazepines. IX. Oxidation of N-Phthalimidoacetylindoles
Benzodiazepines. V. A Novel Synthesis of a 7-Nitro-1,4-benzodiazepine Derivative
Benzodiazepines. XII. Synthesis of 5-(2-Pyridyl)-and 3-Methyl-1,4-benzodiazepin-2-ones
Benzodiazepines. VII. Pyrazino [1,2-α] indole-1 (2H)-ones and Their Conversion to 2,3-Dihydro-1H-1,4-benzodiazepines
Benzodiazepines. VI. A Rearrangement of 2-Aminoacetanilides to Anilinoacetamides
Benzodiazepines. IV. A New Synthesis of 1-Diethylaminoethyl-substituted 1,4-Benzodiazepin-2-ones
Succinimide Derivatives. II. Synthesis and Antipsychotic Activity of N-[4-[4-(1,2-Benzisothiazol-3-yl)-1-piperazinyl]butyl]-1,2-cis-cyclohexanedicarboximide (SM-9018) and Related Compounds
Synthesis and Anxiolytic Activity of N-Substituted Cyclic Imides (1R^*, 2S^*, 3R^*, 4S^*)-N-[4-[4-(2-Pyrimidinyl)-1-piperazinyl]butyl]-2,3-bicyclo[2.2.1]heptanedicarboximide (Tandospirone) and Related Compounds
Heterocage Compound. V. Synthesis of Oxacage Tricyclic Systems : Oxaisotwistane and Oxatwistane Skeleton with an Amino Function
Chemistry of Sodium Borohydride and Diborane. IV. Reduction of Carboxylic Acids to Alcohols with Sodium Borohydride through Mixed Carbonic-Carboxylic Acid Anhydrides
Studies in the Indole Series. III. Steric Inhibition of Resonance in Cycloalkan [b] indolones.
Studies in the Indole Series. II. A General Synthesis of Cycloalkan[b]indolones

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