Next Article in Journal
Molecular Interactions Between the Active Sites of RGD (Arg-Gly-Asp) with its Receptor (Integrine)
Previous Article in Journal
Kinetics of the Aromatic Nucleophilic Substitution Reaction Between 1-Fluoro-2,4-Dinitrobenzene and Perhydroazepine in Ethyl Acetate + Chloroform Solvent Mixtures
Molecules 2000, 5(3), 580-582; doi:10.3390/50300580
Abstract

The Importance of Keto-Enol Forms of Arylpropanoids Acting as Antifungal Compounds

1, 1, 1, 1, 1, 1, 2 and 2
Published: 22 March 2000
Download PDF [17 KB, uploaded 18 June 2014]

Abstract

We report here the importance of a keto-enol equilibrium of an arylpropanoid series acting as antifungal agents. An interesting relationship between ln MIC, ∆E enolization and net atomic charges was found. Two compounds were synthesized and their MIC evaluated in order to prove the above relationship.
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Share & Cite This Article

Further Mendeley | CiteULike
Export to BibTeX |
EndNote
MDPI and ACS Style

Giannini, F.; Devia, C.; Rodríguez, A.; Enriz, R.; Suvire, F.; Baldoni, H.; Furlan, R.; Zacchino, S. The Importance of Keto-Enol Forms of Arylpropanoids Acting as Antifungal Compounds. Molecules 2000, 5, 580-582.

View more citation formats

Related Articles

Article Metrics

Comments

Citing Articles

[Return to top]
Molecules EISSN 1420-3049 Published by MDPI AG, Basel, Switzerland RSS E-Mail Table of Contents Alert