Self condensation of enamines mediated by acetylation. A novel approach to 1-(azol-5-yl)-(1E,3Z)-butadiene-4-N,N-dimethylamines

Org Biomol Chem. 2012 Aug 14;10(30):5795-8. doi: 10.1039/c2ob25331c. Epub 2012 Apr 17.

Abstract

Novel self-condensation of 3-(azol-5-yl)-1,1-dimethylenamines has been found to form new C-C bonds leading to 2,4-(1,2,3-triazole-1,2,3-thiadiazole-3-phenylisothiazole)-(1E,3Z)-5-yl-butadiene-1-amines. The discovered reaction represents a new example of C-H functionalization in unsaturated systems and can serve an efficient synthetic approach to rational design of new 2,4-(diazole-5-yl)-dieneamines.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylation
  • Biphenyl Compounds / chemistry*
  • Diamines / chemical synthesis
  • Diamines / chemistry*
  • Drug Design
  • Imidazoles / chemistry*
  • Substrate Specificity

Substances

  • Biphenyl Compounds
  • Diamines
  • Imidazoles