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dc.contributor.authorKonstantinova, Lidia S.en
dc.contributor.authorBaranovsky, Ilia V.en
dc.contributor.authorStrunyasheva, Vlada V.en
dc.contributor.authorKalogirou, Andreas S.en
dc.contributor.authorPopov, Vadim V.en
dc.contributor.authorLyssenko, Konstantin A.en
dc.contributor.authorKoutentis, Panayiotis A.en
dc.contributor.authorRakitin, Oleg A.en
dc.creatorKonstantinova, Lidia S.en
dc.creatorBaranovsky, Ilia V.en
dc.creatorStrunyasheva, Vlada V.en
dc.creatorKalogirou, Andreas S.en
dc.creatorPopov, Vadim V.en
dc.creatorLyssenko, Konstantin A.en
dc.creatorKoutentis, Panayiotis A.en
dc.creatorRakitin, Oleg A.en
dc.date.accessioned2021-01-25T09:44:46Z
dc.date.available2021-01-25T09:44:46Z
dc.date.issued2018
dc.identifier.urihttp://gnosis.library.ucy.ac.cy/handle/7/63023
dc.description.abstractThermolysis of 4,4&primeen
dc.description.abstract-dichloro-, 4,4&primeen
dc.description.abstract-diaryl-, and 4,4&primeen
dc.description.abstract-di(thien-2-yl)-5,5&primeen
dc.description.abstract-bi(1,2,3-dithiazol-ylidenes) affords the respective 3,6-dichloro-, 3,6-diaryl- and 3,6-di(thien-2-yl)isothiazolo[5,4-d]-isothiazoles in low to high yields. The transformation of the 4,4&primeen
dc.description.abstract-diaryl- and 4,4&primeen
dc.description.abstract-di(thien-2-yl)-5,5&primeen
dc.description.abstract-bi(1,2,3-dithiazolylidenes) occurs at lower temperatures in the presence of the thiophiles triphenylphosphine or tetraethylammonium iodide. Optimized reaction conditions and a mechanistic rationale for the thiophile-mediated ring transformation are presented.en
dc.language.isoenen
dc.sourceMoleculesen
dc.source.urihttps://www.mdpi.com/1420-3049/23/6/1257
dc.titleThe Conversion of 5,5′-Bi(1,2,3-dithiazolylidenes) into Isothiazolo[5,4-d]isothiazolesen
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.3390/molecules23061257
dc.description.volume23
dc.description.issue6
dc.author.faculty002 Σχολή Θετικών και Εφαρμοσμένων Επιστημών / Faculty of Pure and Applied Sciences
dc.author.departmentΤμήμα Χημείας / Department of Chemistry
dc.type.uhtypeArticleen
dc.contributor.orcidKalogirou, Andreas S. [0000-0002-5476-5805]
dc.contributor.orcidKoutentis, Panayiotis A. [0000-0002-4652-7567]
dc.gnosis.orcid0000-0002-5476-5805
dc.gnosis.orcid0000-0002-4652-7567


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