Synthesis of novel beta-lactam fused spiroisoxazolidine chromanones and tetralones as potent antimicrobial agent for human and plant pathogens

Bioorg Med Chem Lett. 2010 Jun 15;20(12):3698-702. doi: 10.1016/j.bmcl.2010.04.084. Epub 2010 Apr 24.

Abstract

Synthesis of novel beta-lactam fused spiroisoxazolidine chromanones and tetralones ring systems has been achieved by intermolecular 1,3-dipolar cycloaddition reaction of bicyclic nitrone with unusual dipolarophiles, arylidene chromanones/tetralones under different reaction conditions. The synthesized compounds were evaluated for antimicrobial activities. It was observed that two of the synthesized compounds exhibited relatively good antibacterial and antifungal activities.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anti-Bacterial Agents / chemical synthesis*
  • Antifungal Agents / chemical synthesis*
  • Chromans / chemical synthesis*
  • Chromans / pharmacology
  • Humans
  • Isoxazoles / chemical synthesis
  • Isoxazoles / pharmacology
  • Microbial Sensitivity Tests
  • Plants / microbiology
  • Spiro Compounds / chemical synthesis
  • Structure-Activity Relationship
  • Tetralones / chemical synthesis*
  • Tetralones / pharmacology
  • beta-Lactams / chemical synthesis*
  • beta-Lactams / pharmacology

Substances

  • Anti-Bacterial Agents
  • Antifungal Agents
  • Chromans
  • Isoxazoles
  • Spiro Compounds
  • Tetralones
  • beta-Lactams