An oxidatively-activated safety catch linker for solid phase synthesis

Org Biomol Chem. 2008 May 7;6(9):1625-34. doi: 10.1039/b802204f. Epub 2008 Mar 14.

Abstract

A N-benzyl-4-amino-2,2-dimethylbutanoic acid-based system has been developed as a new oxidatively activated safety catch linker for reaction monitoring and optimisation on solid support. The CAN promoted oxidative debenzylation of the tertiary N-benzylamine moiety, followed by concomitant cyclisation and release of alcohols and amines has been demonstrated both in solution phase model studies and on the solid phase. The linker system has been applied to the solid phase synthesis of a collection of phenol derivatives, and to the demonstration of the attachment and release of a chiral auxiliary from a solid support.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Combinatorial Chemistry Techniques*
  • Cyclization
  • Molecular Structure
  • Oxidation-Reduction
  • Phenols / chemical synthesis*
  • Phenols / chemistry
  • Stereoisomerism
  • gamma-Aminobutyric Acid / analogs & derivatives*
  • gamma-Aminobutyric Acid / chemistry

Substances

  • Phenols
  • gamma-Aminobutyric Acid