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Sulfur-nitrogen heterocycles from the condensation of pyrazolones and 2-iminothiazolidin-4-ones with phenyl isothiocyanate

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dc.contributor.authorBagdatli, Emine
dc.contributor.authorAkkus, Senem
dc.contributor.authorYolacan, Cigdem
dc.contributor.authorOcal, Nueket
dc.date.accessioned2026-06-27T13:01:45Z
dc.date.issued2007
dc.description.abstractThe condensation of 2-pyrazolin-5-ones with phenyl isothiocyanate, followed by reaction of the resulting thiolate ions with chloroacetyl chloride, phenacyl bromide, oxalyl chloride, 1,4-dibromo-2,3-butanedione and ethyl chloroformate, resulted in cyclisation to S,N-heterocycles in all cases. 2-Iminothiazolidin-4-ones, with phenyl isothiocyanate and then chloroacetyl chloride or phenacyl bromide, similarly formed 2,4 '-bi(thiazolidine)-derived products.en
dc.identifier.eissn2047-6507
dc.identifier.endpage304
dc.identifier.issn1747-5198
dc.identifier.issue5
dc.identifier.startpage302
dc.identifier.urihttps://hdl.handle.net/20.500.14981/49199
dc.identifier.wos000250728900014
dc.language.isoeng
dc.publisherSAGE PUBLICATIONS LTD
dc.relation.ispartofJOURNAL OF CHEMICAL RESEARCH
dc.subjectphenyl isothiocyanate
dc.subject2-pyrazolin-5-ones
dc.subjectthiazolidines
dc.subjectthioanilides
dc.subject1,3-thiazepane-5,6-diones
dc.subjectTRANSFORMATIONS
dc.subjectChemistry
dc.titleSulfur-nitrogen heterocycles from the condensation of pyrazolones and 2-iminothiazolidin-4-ones with phenyl isothiocyanate
dc.typeArticle
dspace.entity.typePublication
local.import.sourceWOS

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