Publication:
A study on ester thiosemicarbazones

dc.contributor.authorsIkizler A.A., Kahveci B., Johansson C.B., Celik C., Yüksek H.
dc.date.accessioned2022-03-28T14:50:15Z
dc.date.accessioned2026-01-11T06:45:59Z
dc.date.available2022-03-28T14:50:15Z
dc.date.issued1997
dc.description.abstractThe cyclization of ester thiosemicarbazones to two different heterocycles was studied for some new thiosemicarbazones, and only the formation of 1,2,4-triazol-5-thiols was attributed to the regioselectivity of the ring closure reaction, due to a steric hindrance of bulky groups. Next, some of the new compounds were tested for their in vitro antimicrobial and antitumor activities.
dc.identifier.issn16837
dc.identifier.pubmed9511459
dc.identifier.urihttps://hdl.handle.net/11424/255377
dc.language.isoeng
dc.relation.ispartofActa Poloniae Pharmaceutica - Drug Research
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subject1,2,4-triazol-5-thiols
dc.subject1,3,4-thiadiazoles
dc.subject4,5-dihydro-1h-1,2,4-triazol-5-thiones
dc.subjectBiological activity
dc.subjectEster thiosemicarbazones
dc.subjectSynthesis
dc.titleA study on ester thiosemicarbazones
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage312
oaire.citation.issue4
oaire.citation.startPage307
oaire.citation.titleActa Poloniae Pharmaceutica - Drug Research
oaire.citation.volume54

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