Synthesis and Biological Activity of New 1,3-Dioxolanes as Potential Antibacterial and Antifungal Compounds

Kucuk H. B., Yusufoglu A. S., Mataraci E., Dosler S.

MOLECULES, vol.16, no.8, pp.6806-6815, 2011 (SCI-Expanded) identifier identifier identifier

  • Publication Type: Article / Article
  • Volume: 16 Issue: 8
  • Publication Date: 2011
  • Doi Number: 10.3390/molecules16086806
  • Journal Name: MOLECULES
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Page Numbers: pp.6806-6815
  • Keywords: 1,3-dioxolanes, montmorillonite K10, diols, antibacterial activity, antifungal activity, ASYMMETRIC-SYNTHESIS, CARBONYL-COMPOUNDS, DERIVATIVES, INHIBITORS, ACETALS, KETALS
  • Istanbul University Affiliated: Yes

Abstract

A series of new enantiomerically pure and racemic 1,3-dioxolanes 1-8 was synthesized in good yields and short reaction times by the reaction of salicylaldehyde with commercially available diols using a catalytic amount of Mont K10. Elemental analysis and spectroscopic characterization established the structure of all the newly synthesized compounds. These compounds were tested for their possible antibacterial and antifungal activity. Biological screening showed that all the tested compounds, except 1, show excellent antifungal activity against C. albicans, while most of the compounds have also shown significant antibacterial activity against S. aureus, S. epidermidis, E. faecalis and P. aeruginosa.