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Regioselective O- glykosylering af Nukleosider via den midlertidige 2', 3'-Diol beskyttelse af en Boronic Ester til syntese af disaccharid Nukleosider
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Regioselective O- glykosylering af Nukleosider via den midlertidige 2', 3'-Diol beskyttelse af en Boronic Ester til syntese af disaccharid Nukleosider

Article DOI: 10.3791/57897-v • 08:46 min • July 26th, 2018
July 26th, 2018 •
1, 1, 1, 1,2
1Faculty of Pharmaceutical Sciences, Tokyo University of Science, 2Imaging Frontier Center, Tokyo University of Science

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Her, vi præsenterer protokoller til syntese af disaccharid Nukleosider af regioselective O- glykosylering af ribonucleosides via en midlertidig beskyttelse af deres 2', 3'-diol fraspaltning udnytter en cyklisk boronic ester. Denne metode gælder for flere ubeskyttede Nukleosider adenosin, Guanosinmonofosfat, cytidine, uridine, 5-methyluridine og 5-fluorouridine til at give tilsvarende disaccharid Nukleosider.

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Kemi sag 137 disaccharid Nukleosider O- glykosylering ribonucleosides midlertidig beskyttelse thioglycosides cyklisk boronic ester
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