砂川洵 | Research Center, Sumitomo Pharmaceuticals Co., Ltd.,

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著作論文

Stability of a 1β-Methylcarbapenem Antibiotic, Meropenem (SM-7338) in Aqueous Solution
The Stability of a Novel Carbapenem Antibiotic, Meropenem (SM-7338), in a Solid State Formulation for Injection
Synthetic Studies of Carbapenem and Penem Antibiotics. IV. Stereoselective Reduction of 3-Acetyl-2-azetidinone with Aminoalkoxyborane
Synthetic Studies of Carbapenem and Penem Antibiotics. III. A Synthesis of a Key Intermediate for 1β-Methylcarbapenem
Synthetic Studies of Carbapenem and Penem Antibiotics. II. Synthesis of 3-Acetyl-2-azetidinones by (2+2) Cycloaddition of Diketene and Schiff Bases
Synthetic Studies of Carbapenem and Penem Antibiotics. I. Facile Synthesis of a Key Intermediate : 4-Acetoxy-3-(1-hydroxyethyl)-2-azetidinone
Dibenzotetracyclic Derivatives. II. Synthesis of 9-Aminoalkyl-9,10-dihydro-9,10-methanoanthracenes
Dibenzotetracyclic Derivatives. III. Synthesis of 9-γ-Methylaminopropyl-9,10-dihydro-9,10-propanoanthracene
Studies of Cyclodextrin Inclusion Complexes. II. Application of the Partition Coefficient Method
Studies of Cyclodextrin Inclusion Complexes. I. Complex between Cyclodextrins and Bencyclane in Aqueous Solution
Synthetic Studies of Carbapenem and Penem Antibiotics. VI. Stereoselective Reduction of Enamino Ketone and Lactonization of the Reduction Product for the Synthesis of 1β-Methylcarbapenem

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