堀田清 | Faculty Of Pharmaceutical Sciences Health Science University Of Hokkaido

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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)
P-46 海洋産ポリエーテルマクロリド、ハリコンドリンBの全合成研究(ポスター発表の部)
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
24 海洋産ポリエーテルマクロリド、ハリコンドリンBの全合成研究(口頭発表の部)
光学活性な天然ホスト分子としてのポリエーテル抗生物質
Sythesis of Erythronolide A via Direct Macrolactonization of a Conformationally Controlled Seco-acid with the Yamaguchi Reagent in the Presence of Dimethylaminopyridine
25 ポリエーテル抗生物質リソセリンの立体選択的全合成(口頭発表の部)
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
62(PA2-2) ポリエーテル系抗生物質イソラサロシドAとラサロシドAの合成研究(ポスター発表の部)
71 イオノフォアポリエーテル抗生物質リリノマイシンの立体選択的合成
Synthetic Studies on Halichondrin B, an Antitumor Polyether Macrolide Isolated from a Marine Sponge. 9. Synthesis of the C16-C36 Unit via Stereoselective Construction of the D and E Rings
Synthetic Studies of Halichondrin B, an Antitumor Polyether Macrolide Isolated from a Marine Sponge. 7. Synthesis of Two C27-C36 Units via Construction of the F Ring and Completely Stereoselective C-Glycosylation Using Mixed Lewis Acids
Synthesis of Macrocyclic Amides. Formation of a New Symmetric 36-Membered Tetramide Ring

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