ミヤザキ タツオ
Tatsuo Miyazaki
宮﨑 達雄 所属 新潟薬科大学 応用生命科学部 応用生命科学科 職種 准教授 |
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言語種別 | 英語 |
発行・発表の年月 | 2018 |
形態種別 | 論文 |
査読 | 査読あり |
標題 | Synthesis of 5a,5a'-dicarba-D-glucobioses from conformationally restricted carbaglucosyl triflates using SN2-type inversion with carbaglucosyl nucleophiles. |
執筆形態 | 共著 |
掲載誌名 | Bioorganic & medicinal chemistry |
掲載区分 | 国外 |
著者・共著者 | Tateda Naoya, Ajisaka Katsumi, Ishiguro Masaji, Miyazaki Tatsuo |
概要 | Novel carbohydrate mimics were designed which contain two 5a-carba-d-glucose residues, one each at reducing and nonreducing end, and thus these mimics are 5a,5a'-dicarba-d-glucobioses. Dicarbadisaccharides have attractive features such as stability against endogenous degradative enzymes and being resistant to glycation reactions such as the Maillard reaction. For the synthesis of dicarba-β-d-isomaltose derivatives, the carbaglucosyl triflate locked in 4C1 conformation was synthesized by protecting with butane-2,3-diacetal group or benzylidene group. Then, 5a,5a'-dicarba-β-d-maltose and 5a,5a'-dicarba-α,β-d-trehalose were synthesized by the SN2-type inversion reaction using 4,6-O-benzylidene carbaglucosyl triflate with 4-OH and 1-OH carba-β-d-glucose derivatives, respectively, and similarly 5a,5a'-dicarba-α-d-isomaltose with 6-OH carba-α-d-glucose derivative. |
DOI | 10.1016/j.bmc.2018.12.027 |
ISSN | 1464-3391 |
PMID | 30606671 |