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dc.contributor.authorMataraci, Emel
dc.contributor.authorDosler, Sibel
dc.contributor.authorYusufoglu, Ayşe Sergüzel
dc.contributor.authorKucuk, Hatice Baspinar
dc.date.accessioned2021-03-03T09:21:08Z
dc.date.available2021-03-03T09:21:08Z
dc.date.issued2011
dc.identifier.citationKucuk H. B. , Yusufoglu A. S. , Mataraci E., Dosler S., "Synthesis and Biological Activity of New 1,3-Dioxolanes as Potential Antibacterial and Antifungal Compounds", MOLECULES, cilt.16, sa.8, ss.6806-6815, 2011
dc.identifier.issn1420-3049
dc.identifier.otherav_1c98cdde-f828-4e22-8cfa-c1b5202c30e7
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/24460
dc.identifier.urihttps://doi.org/10.3390/molecules16086806
dc.description.abstractA 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.
dc.language.isoeng
dc.subjectSitogenetik
dc.subjectBiyokimya
dc.subjectAlkoloidler
dc.subjectTemel Bilimler
dc.subjectYaşam Bilimleri
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectTemel Bilimler (SCI)
dc.subjectKimya
dc.subjectKİMYA, MULTİDİSİPLİNER
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectBİYOKİMYA VE MOLEKÜLER BİYOLOJİ
dc.titleSynthesis and Biological Activity of New 1,3-Dioxolanes as Potential Antibacterial and Antifungal Compounds
dc.typeMakale
dc.relation.journalMOLECULES
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.identifier.volume16
dc.identifier.issue8
dc.identifier.startpage6806
dc.identifier.endpage6815
dc.contributor.firstauthorID6503


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