Complementary chemoenzymatic routes to both enantiomers of febrifugine

Org Biomol Chem. 2009 Jul 21;7(14):2976-80. doi: 10.1039/b901670h. Epub 2009 Jun 4.

Abstract

Two complementary strategies for the synthesis of febrifugine are detailed based on previously developed chemoenzymatic approaches to the 3-hydroxypiperidine skeleton. The introduction of the quinazolone-containing side chain in both strategies was based on an N-acyliminium ion-mediated coupling reaction.

MeSH terms

  • Catalysis
  • Piperidines / chemical synthesis*
  • Piperidines / chemistry
  • Quinazolines / chemical synthesis*
  • Quinazolines / chemistry
  • Stereoisomerism
  • Substrate Specificity

Substances

  • Piperidines
  • Quinazolines
  • febrifugine