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Automated Electrochemical Assembly of the Protected Potential TMG-chitotriomycin Precursor Based on Rational Optimization of the Carbohydrate Building Block

Toshiki NokamiYuta IsodaNorihiko SasakiAki TakaisoShuichi HayaseToshiyuki ItohRyutaro HayashiDepartment of Synthetic Chemistry and Biological Chemistry, Graduate School of Engineering, Kyoto University, Kyoto-daigaku-Katsura, Nishikyo-ku, Kyoto 615-8510, JapanAkihiro ShimizuDepartment of Synthetic Chemistry and Biological Chemistry, Graduate School of Engineering, Kyoto University, Kyoto-daigaku-Katsura, Nishikyo-ku, Kyoto 615-8510, JapanJun‐ichi YoshidaDepartment of Synthetic Chemistry and Biological Chemistry, Graduate School of Engineering, Kyoto University, Kyoto-daigaku-Katsura, Nishikyo-ku, Kyoto 615-8510, Japan
2015en
ABI

Аннотация

The anomeric arylthio group and the hydroxyl-protecting groups of thioglycosides were optimized to construct carbohydrate building blocks for automated electrochemical solution-phase synthesis of oligoglucosamines having 1,4-β-glycosidic linkages. The optimization study included density functional theory calculations, measurements of the oxidation potentials, and the trial synthesis of the chitotriose trisaccharide. The automated synthesis of the protected potential N,N,N-trimethyl-d-glucosaminylchitotriomycin precursor was accomplished by using the optimized building block.

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