Mimicking dihydroxy acetone phosphate-utilizing aldolases through organocatalysis: a facile route to carbohydrates and aminosugars

Org Lett. 2005 Mar 31;7(7):1383-5. doi: 10.1021/ol0502533.

Abstract

[reaction: see text] A practical and environmentally friendly organocatalytic strategy designed to mimic the DHAP aldolases has been developed and shown to be effective in the preparation of carbohydrates and aminosugars. (S)-Proline and (S)-2-pyrrolidine-tetrazole catalyzed the aldol reaction between dihydroxy acetone variants such as 1,3-dioxan-5-one and 2,2-dimethyl-1,3-dioxan-5-one with aldehydes to give the corresponding polyols in good yields with very high ees.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Aldehyde-Lyases / chemistry
  • Aldehyde-Lyases / metabolism*
  • Amino Sugars / chemical synthesis*
  • Carbohydrates / chemical synthesis*
  • Catalysis
  • Molecular Mimicry
  • Molecular Structure

Substances

  • Amino Sugars
  • Carbohydrates
  • Aldehyde-Lyases