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Rapid Stereochemical Analysis of Glycosylations in Flow by Ion Mobility Spectrometry

Jakob B. Wolf, Martin Zühlke, Dominik Weh, Marlene C.S. Dal Colle, Christian Thoben, Toralf Beitz, Klaus Bienert, Dario Cambié, Eric T. Sletten, Martina Delbianco, Stefan Zimmermann*, Peter H. Seeberger*

*Corresponding author for this work

Research output: Contribution to journalArticleResearchpeer review

Abstract

Glycans are biologically important molecules that are difficult to synthesize and analyze due to their structural diversity and conformational flexibility. Stereoselective glycosylation reactions are key to achieving high-yielding glycan syntheses. The stereochemical outcome of glycosylations is significantly influenced by factors such as the choice of activator and leaving group systems, solvent type, temperature, concentration, and stoichiometry. We introduce a flow chemistry approach to efficiently screen glycosylation conditions, using minimal material and time to enable a rapid design-make-test-analyze cycle with precise parameter control for reaction optimization. Ion mobility spectrometry provides rapid separation and analysis of crude glycosylation reaction mixtures that requires less method development than liquid chromatography thus making it a valuable tool for optimizing glycosylation reactions.

Original languageEnglish
Article numbere202500311
JournalChemistry - a European journal
Volume31
Issue number25
E-pub ahead of print20 Mar 2025
DOIs
Publication statusPublished - 7 May 2025

Keywords

  • chemical glycosylation
  • flow chemistry
  • ion mobility spectrometry
  • reaction screening
  • stereoselectivity

ASJC Scopus subject areas

  • Catalysis
  • General Chemistry
  • Organic Chemistry

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