One-step synthesis of oxazoline and dihydrooxazine libraries

J Comb Chem. 2007 May-Jun;9(3):473-6. doi: 10.1021/cc060159t. Epub 2007 Mar 29.

Abstract

The reactions of 1,2- and 1,3-hydroxyalkyl azides and aldehydes in the presence of Lewis acid result in the one-step construction of oxazolines and dihydrooxazines, respectively. The reaction was adapted to parallel synthesis using a polymer-bound phosphine to scavenge excess hydroxyalkyl azide. Thus, a 60-member library of various disubstituted oxazolines and di- and trisubstituted dihydrooxazines was generated.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Combinatorial Chemistry Techniques / methods*
  • Molecular Structure
  • Oxazines / chemical synthesis*
  • Oxazines / chemistry
  • Oxazoles / chemical synthesis*
  • Oxazoles / chemistry
  • Stereoisomerism

Substances

  • Oxazines
  • Oxazoles