Publication:
Synthesis and evaluation of some substituted 1,3,4-thiadiazole derivatives

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dc.contributor.authorsGulerman N., Rollas S., Ulgen M., Gorrod J.W.
dc.date.accessioned2022-03-28T14:50:03Z
dc.date.accessioned2026-01-10T19:54:01Z
dc.date.available2022-03-28T14:50:03Z
dc.date.issued1995
dc.description.abstract5-[p-(acetylamino)phenyl]-2-substitutedamino-1,3,4-thiadiazole derivatives were prepared by the cyclisation reaction of sulphuric acid on 1-[p-(aminoacetyl)phenyl]-4-alkyl/arylthiosemicarbazides. The intermediate thio semicarbazides were formed by the condensation of p-(acetylamino)benzoylhydrazine with corresponding isothiocyanates. The structures of the compounds were elucidated by use of their IR, 1H NMR and mass spectral data.
dc.identifier.issn66648
dc.identifier.urihttps://hdl.handle.net/11424/255296
dc.language.isoeng
dc.relation.ispartofBollettino Chimico Farmaceutico
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subject1,3,4-thiadiazoles
dc.subjectthiosemicarbazides
dc.titleSynthesis and evaluation of some substituted 1,3,4-thiadiazole derivatives
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage463
oaire.citation.issue8
oaire.citation.startPage461
oaire.citation.titleBollettino Chimico Farmaceutico
oaire.citation.volume134

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