Expedient and versatile formation of novel amino-deoxy-ketoheptuloses

Org Lett. 2013 Oct 4;15(19):4948-51. doi: 10.1021/ol4021699. Epub 2013 Sep 13.

Abstract

Novel monoketoheptuloses have been synthesized employing an amination step in a pre- and/or post-C1 chain elongation using a Petasis reagent by starting from aldohexoses or aldohexosamines. A series of gluco and manno configured 1-/3-deoxy-1-/3-amino-ketohept-2-uloses could be obtained.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amination
  • Heptoses / chemical synthesis*
  • Heptoses / chemistry
  • Ketoses / chemical synthesis*
  • Ketoses / chemistry
  • Molecular Structure

Substances

  • Heptoses
  • Ketoses