米光宰 | 岡山理大理

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P-43 16員環マクロリド・ヒグロリド類の全合成研究(ポスター発表の部)
A Stereoselective Total Synthesis of (9S)-9-Dihydroerythronolide A via Coupling between the Right-Half (C1-C6) Aldehyde and the Left-Half (C7-C15) Sulfoxide
Synthetic Study of (9S)-9-Dihydroerythronolide A via Witting-Horner Coupling of C1-C6 and C7-C15 Segments
Alternative Syntheses of the C9-C15 and C1-C5 Segments of Erythronolide A via Regio- and Stereo-Selective Reductive Ring Opening of 2,3-Epoxy Alcohols
3-METHOXYBENZYL (3-MPM) ABD 3,5-DIMETHOXYBENZYL (3,5-DMPM) PROTECTING GROUPS FOR THE HYDROXY FUNCTION LESS READILY REMOVABLE THAN 4-METHOXYBENZYL (MPM)AND 3,4-DIMETHOXYBENZYL (DMPM) PROTECTING GROUPS BY DDQ OXIDATION
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)
41 14員環マクロリドのセコ酸誘導体の立体配座計算とマクロラクトン化(口頭発表の部)
51 高立体選択的ヘテロジールスアルダー反応の開発とポリアミン系アルカロイドカンナビサチビンの合成への応用(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
69 エリスロノリドAの改良合成(口頭発表の部)
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
Stereoselective Total Synthesis of 16-Membered Macrolide Aglycons, Leuconolides and Maridonolides. Macrocylic Stereocontrol Based on Conformational Analysis of the 16-Membered Macrolide Ring
31 環上での立体制御反応を利用した16員環マクロリド類の合成(口頭発表の部)
113(P-42) 抗腫瘍活性18員環マクロリド・テダノリドの全合成研究(ポスター発表の部)
Synthesis of Macrocyclic Amides. Formation of a New Symmetric 36-Membered Tetramide Ring
Facile Total Synthesis of Carbonolides by Witting-Hoener Macro-Cyclization and Stereoselective Epoxidation
マクロリド合成
Highly Stereoselective Total Synthesis of Pikronolide, the Aglycon of the First Macrolide Antibiotic Pikroraycin. Crucial Role of Benzyl-Type Protecting Groups Removable by 2,4-Dichloro-5,6-dicyanobenzoquinone Oxidation(Organic,Chemical)
Highly Stereoselective Total Synthesis of Methynolide, the Aglycon of the 12-Membered Macrolide Antibiotic Methymycin. III. An Efficient Synthesis of Methynolide(Organic,Chemical)
43 Wittig-Horner反応による閉環をキーステップとするマクロリド抗生物質の合成 : メチノリド・ピクロノリド・タイロノリドの高立体選択的合成
112(P48) 紅藻由来の環状ポリケタイド化合物の合成研究(ポスター発表の部)

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