AI Article Synopsis

  • Glycosidic bond formation is a complex process for chemists, and this study focuses on improving the efficiency of oligosaccharide synthesis by examining how glycosyl donor activation relates to reaction temperature.
  • Using a novel semi-automated assay, researchers found that different thioglycosides react variably to temperature changes due to their protecting groups and thiol aglycon structures.
  • The introduction of a "donor activation temperature" allows for better control over glycosylation reactions, resulting in a significant reduction in the amount of building blocks needed, improving overall efficiency compared to traditional methods.

Article Abstract

Glycosidic bond formation is a continual challenge for practitioners. Aiming to enhance the reproducibility and efficiency of oligosaccharide synthesis, we studied the relationship between glycosyl donor activation and reaction temperature. A novel semi-automated assay revealed diverse responses of members of a panel of thioglycosides to activation at various temperatures. The patterns of protecting groups and the thiol aglycon combine to cause remarkable differences in temperature sensitivity among glycosyl donor building blocks. We introduce the concept of donor activation temperature to capture experimental insights, reasoning that glycosylations performed below this reference temperature evade deleterious side reactions. Activation temperatures enable a simplified temperature treatment and facilitate optimization of glycosyl donor usage. Isothermal glycosylation below the activation temperature halved the equivalents of building block required in comparison to the standard "ramp" regime used in solution- and solid-phase oligosaccharide synthesis to-date.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9306470PMC
http://dx.doi.org/10.1002/anie.202115433DOI Listing

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