堀田清 | Faculty of Pharmaceutical Sciences, Hokkaido University

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著作論文

Highly Stereoselective Total Synthesis of Methynolide, the Aglycon of the 12-Membered Macrolide Antibiotic Methymycin. I. Synthesis of a Prelog-Djerassi Lactone-Type Chiral Intermediate from D-Glucose(Organic,Chemical)
Large Laboratory Scale Synthesis of (2S, 3S)-2-(4-Methoxybenzyloxy)-3,4-O-(3-pentylidene)-1,3,4-butantriol, a Versatile Chiral Building Block in Natural Product Synthesis
Stereoselective Synthesis of Optically Active 4-Ethyl-3,5-dihydroxy-2-methylpentyl Derivatives. A Basic Building Block with Three Contiguous Chiral Centers of Polyether Antibiotics
Highly Stereocontrolled Total Synthesis of the Polyether Antibiotic Salinomycin. IV. Chemical Degradation of Salinomycin for the Structure Confirmation of Synthesic Key Intermediates
Highly Stereocontrolled Total Synthesis of the Polyether Antibiotic Salinomycin. III. Total Synthesis of Salinomycin via Coupling of C1-C9,C10-C17,and C18-C30 Segments
Highly Stereocontrolled Total Synthesis of the Polyether Antibiotic Salinomycin. II. Synthesis of Right (C18-C30) Segments from D-Glucose, D-Mannitol, and Ethyl L-Lactate
Highly Stereocontrolled Total Synthesis of the Polyether Antibiotic Salinomycin. I. Synthesis of the Left (C1-C9) and Middle (C10-C17) Segments from D-Glucose
Synthesis of Macrocyclic Amides. Formation of a New Symmetric 36-Membered Tetramide Ring

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