Abstract
Various 5’-β-saccharides of pyridoxine, namely the mannoside, galactoside, arabinoside, maltoside, cellobioside and glucuronide, were synthesized chemically according to KOENIGS-KNORR conditions using α4,3-O-isopropylidene pyridoxine and the respective acetobromo glycosyl donors with AgOTf (3.0 eq.) and NIS (3.0 eq.) as promoters at 0 °C. Furthermore, 5’-β-[13C6]-labeled pyridoxine glucoside (PNG) was prepared starting from [13C6]-glucose and pyridoxine. Additionally, two strategies were examined for the synthesis of 5’-β-pyridoxal glucoside (PLG).
Original language | English |
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Article number | 107940 |
Journal | Carbohydrate Research |
Volume | 489 |
DOIs | |
State | Published - Mar 2020 |
Keywords
- Chemical synthesis
- Glycoconjugates
- Glycosylation
- Labeled
- PLG
- PNG
- Pyridoxal
- Pyridoxine
- Vitamin B