Pregled bibliografske jedinice broj: 1222637
Novel Synthetic Routes to Quaternary Pyridinium Salts and their Antifungal Activity
Novel Synthetic Routes to Quaternary Pyridinium Salts and their Antifungal Activity // Croatica chemica acta, 95 (2022), 1; 31-38 doi:10.5562/cca3903 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 1222637 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Novel Synthetic Routes to Quaternary Pyridinium
Salts and their Antifungal Activity
Autori
Bušić, Valentina ; Vrandečić, Karolina ; Siber, Tamara ; Roca, Sunčica ; Tomičić, Vice ; Gašo- Sokač, Dajana
Izvornik
Croatica chemica acta (0011-1643) 95
(2022), 1;
31-38
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
antifungal activity ; dihaloalkanes ; deep eutectic solvents ; microwave synthesis ; quaternization ; pyridine derivatives ; ultrasound synthesis
Sažetak
Eleven pyridine derivatives were prepared by quaternization reactions by different synthetic routes: conventional, microwave, and ultrasound. Since acetone and other solvents used in conventional quaternization reactions are harmful, attempts were made to replace the organic solvents with more environmentally friendly alternative - deep eutectic solvents. The reactions were carried out using pyridine-3-aldoxime, pyridine-4- aldoxime, isonicotinamide and nicotinamide as nucleophiles and three different dihaloalkanes as electrophiles: diiodopropane, dibromopropane and diiodohexane. The results showed that the microwave method using acetone as solvent was significantly faster and gave higher yields than the conventional method. In contrast, synthesis in the eutectic solvents choline chloride : urea gave significantly lower yields. The structures of the synthesized compounds were confirmed by 1H and 13C NMR spectroscopy, mass spectrometry and elemental analysis. The antifungal activity of all compounds was tested at two different concentrations (10 and 100 µg mL–1) against Botrytis cinerea, Fusarium culmorum, Macrophomina phaseolina and Sclerotinia sclerotiorum in vitro. All tested compounds showed excellent inhibitory activity against the studied phytopathogenic fungal species at a concentration of 100 µg mL–1.
Izvorni jezik
Engleski
Znanstvena područja
Kemija, Poljoprivreda (agronomija)
POVEZANOST RADA
Ustanove:
Fakultet agrobiotehničkih znanosti Osijek,
Institut "Ruđer Bošković", Zagreb,
Prehrambeno-tehnološki fakultet, Osijek
Profili:
Valentina Bušić (autor)
Tamara Siber (autor)
Dajana Gašo-Sokač (autor)
Sunčica Roca (autor)
Vice Tomičić (autor)
Karolina Vrandečić (autor)
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus