4.6 Article

Reagent switchable stereoselective beta(1,2) mannoside mannosylation: OH-2 of mannose is a privileged acceptor

Journal

ORGANIC & BIOMOLECULAR CHEMISTRY
Volume 6, Issue 15, Pages 2692-2696

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/b803999m

Keywords

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Funding

  1. Biotechnology and Biological Sciences Research Council [BB/C510824/1] Funding Source: researchfish
  2. Engineering and Physical Sciences Research Council [EP/E000614/1, EP/D023335/1, GR/T26542/01, EP/D023343/1] Funding Source: researchfish
  3. Biotechnology and Biological Sciences Research Council [EGA17763, BB/E004350/1] Funding Source: Medline
  4. BBSRC [BB/E004350/1] Funding Source: UKRI
  5. EPSRC [EP/E000614/1] Funding Source: UKRI

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The discovery of novel conditions for highly beta-stereoselective (>9 : 1) mannosylation of OH-2 of mannosides using a straightforward perbenzylthioglycoside donor has allowed ready assembly of beta-mannosyl oligosaccharides including the repeating trisaccharide motif of the O5 antigen of pathogen Klebsiella pneumoniae.

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