Bohlmann-Rahtz cyclodehydration of aminodienones to pyridines using N-iodosuccinimide

Molecules. 2010 Apr 30;15(5):3211-27. doi: 10.3390/molecules15053211.

Abstract

Cyclodehydration of Bohlmann-Rahtz aminodienone intermediates using N-iodosuccinimide as a Lewis acid proceeds at low temperature under very mild conditions to give the corresponding 2,3,6-trisubstituted pyridines in high yield and with total regiocontrol.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amines
  • Ketones
  • Pyridines / chemical synthesis*
  • Succinimides / chemistry*
  • Temperature

Substances

  • Amines
  • Ketones
  • Pyridines
  • Succinimides
  • N-iodosuccinimide