Hara Osamu | Pharmaceutical Research Center Meiji Seika Kaisha Ltd.

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Cladinose Analogues of Sixteen-membered Macrolide Antibiotics VI. Synthesis of metabolically Programmed, Highly Potent Analogues of Sixteen-membered Macrolide Antibiotics
Cladinose Analogues of Sixteen-membered Macrolide Antibiotics V. Preparation of Unsubstituted L-Cladinose Analogues: Effect of Methylation of a 3''-Hydroxyl Group on the Bioactivity
Cladinose Analogues of Sixteen-membered Macrolide Antibiotics IV. Improved Therapeutic Effects of 4-O-Acyl-L-cladinose Analogues of Sixteen-membered Macrolide Antibiotics
Cladinose Analogues of Sixteen-membered Macrolide Antibiotics II. Preparation of Pharmacokinetically Improved Analogues via Biotransformation
Cladinose Analogues of Sixteen-membered Macrolide Antibiotics I. Synthesis of 4-O-Alkyl-L-cladinose Analogues via Glycosylation
Studies on the Biosynthesis of Bialaphos. Biochemical Mechanism of C-P Bond Formation: Discovery of Phosphonopyruvate Decarboxylase which Catalyzes the Formation of Phosphonoacetaldehyde from Phosphonopyruvate
Biochemical Mechanism of C-P Bond Formation of Bialaphos : Use of Gene Manipulation for the Analysis of the C-P Bond Formation Step(Biological Chemistry)

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