Sinteza tiadiazina s kumarinskom jezgrom kao potrencijalnih inhibitora rasta nekih mikotoksikogenih plijesni (CROSBI ID 366645)
Ocjenski rad | diplomski rad
Podaci o odgovornosti
Grabar, Vesna
Čačić, Milan
Molnar, Maja
hrvatski
Sinteza tiadiazina s kumarinskom jezgrom kao potrencijalnih inhibitora rasta nekih mikotoksikogenih plijesni
Derivati kumarina (2H-kromen-2-ona) su heterociklicki spojevi, a mnogi od njih imaju izražene biološke aktivnosti. Sadrže 2-pironsku jezgru kondenziranu sa benzenskim prstenom. Uglavnom se nalaze u biljnim vrstama. Spojevi s kumarinskom jezgrom su zbog svog inhibitornog djelovanja na rast odredenih mikroorganizama našli primjenu u medicini, prehrambenoj i farmaceutskoj industriji. Posebna pozornost ovog rada je usmjerena na dizajn i sintezu novih tiadiazina iz supstituiranih kumarinskih tiosemikarbazida. Tiadiazini su takoder biološki aktivni spojevi s antivirusnim, antitumornim, antituberkuloznim i drugim djelovanjima. Reakcijom kondenzacije 3--bromoacetilkumarina sa odgovarajucim tiosemikarbazidima priredeni su razliciti tiadiazini koji dosad nisu opisani u literaturi. Dobiveni spojevi su procišceni prekristalizacijom te su im odredene tocke tališta i elementarni sastav. Struktura pojedinih spojeva potvrdena je 1H-NMR i IR spektrometrijom te spektrometrijom masa.
kumarin ; tiadiazin ; mikotoksini; biološka aktivnost
nije evidentirano
engleski
Synthesis of thiadizine with the coumarine core as a potential growth inhibitor of some mycotoxigen moulds
The coumarine derivatives (2H-chromen-2-ones) are heterocyclic compounds, many of whom have significant biological activities. They contain 2-pyrone core that is condensed with the benzen ring. They can mostly be found in herbal species.Coumarine core based compounds are very useful in medicine, food and pharmaceutical industry, due to its specific inhibitory effects on the growth of specific microorganisms. This paper focuses special attention on the design and synthesis of the new thiadiazine from substitued coumarine thisemicarbazides. Thiadizine are also biologicly active compounds with antiviral, antitumor, antituberculosis and other effects. By reacting the condensed 3--bromoacetylcoumarine with the matching thiosemicarbazides, there were some varieties of thiadiazine created that have not been described in literature. The reaction progress was monitored with a thin layer chromotography, the attained compounds were purified by recrystallization and the specific points of melting, as well as their composition, were determined. The structure of particular compounds was confirmed with 1H-NMR i IR spectrometry, as well as with mass spectrometry.
coumarine; thiadiazine; thiosemicarbazide; biological activity; mycotoxine
nije evidentirano
Podaci o izdanju
60
14.05.2010.
obranjeno
109:495276
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