Regioselective synthesis and antimicrobial screening of novel ketocarbazolodispiropyrrolidine derivatives

Eur J Med Chem. 2009 Mar;44(3):959-66. doi: 10.1016/j.ejmech.2008.07.009. Epub 2008 Jul 18.

Abstract

A series of novel dispiropyrrolidine derivatives have been synthesized through 1,3-dipolar cycloaddition reaction of azomethine ylide generated from sarcosin and di/tri ketone with the dipolarophile (E)-2-arylidine-1-keto-carbazoles. The cycloadducts ketocarbazalo spiro N-methyl pyrrolidines showed the most interesting antimicrobial activity at lower concentration.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anti-Bacterial Agents / chemical synthesis*
  • Anti-Bacterial Agents / chemistry
  • Anti-Bacterial Agents / pharmacology*
  • Microbial Sensitivity Tests
  • Models, Molecular
  • Proteus vulgaris / drug effects
  • Pyrrolidines / chemical synthesis*
  • Pyrrolidines / chemistry
  • Pyrrolidines / pharmacology*
  • Salmonella typhi / drug effects
  • Spectrometry, Mass, Electrospray Ionization
  • Spectroscopy, Fourier Transform Infrared
  • Staphylococcus aureus / drug effects

Substances

  • Anti-Bacterial Agents
  • Pyrrolidines