Chemical synthesis of 5’-β-glycoconjugates of vitamin B6

Thomas Bachmann, Christian Schnurr, Laura Zainer, Michael Rychlik

Research output: Contribution to journalArticlepeer-review

1 Scopus citations

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 languageEnglish
Article number107940
JournalCarbohydrate Research
Volume489
DOIs
StatePublished - Mar 2020

Keywords

  • Chemical synthesis
  • Glycoconjugates
  • Glycosylation
  • Labeled
  • PLG
  • PNG
  • Pyridoxal
  • Pyridoxine
  • Vitamin B

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