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dc.contributor.authorKoutentis, Panayiotis Andreasen
dc.contributor.authorRees, C. W.en
dc.creatorKoutentis, Panayiotis Andreasen
dc.creatorRees, C. W.en
dc.date.accessioned2019-11-21T06:20:55Z
dc.date.available2019-11-21T06:20:55Z
dc.date.issued2002
dc.identifier.issn1472-7781
dc.identifier.urihttp://gnosis.library.ucy.ac.cy/handle/7/55733
dc.description.abstract6-Chloro-1,2,3-benzodithiazolium chlorides 1 (Herz salts) react with malononitrile to afford the highly coloured ylidenes 2 in low to moderate yields. The reaction is general but complex and in the case of the 6-chloro-4-methoxy-1,2,3-benzodithiazolium chloride 1e the by-products 6-chloro-4-methoxy-1,3-benzothiazole-2-carbonitrile 3, 6-chloro-4-methoxy-2,3-dihydro-1,3-benzothiazole-2,2-dicarbonitrile 4, and 4-methoxy-6-thiocyanato-1,3-benzothiazole-2-carbonitrile 5 were also isolated.en
dc.sourceJournal of the Chemical Society.Perkin Transactions 1en
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-0036007704&doi=10.1039%2fb110024f&partnerID=40&md5=d6123d88a4fc253c05d1b9ee15dbf812
dc.subjectChromatographyen
dc.subjectSynthesis (chemical)en
dc.subjectCrystallizationen
dc.subjectUltraviolet radiationen
dc.subjectNuclear magnetic resonanceen
dc.subjectSolventsen
dc.subjectOrganic compoundsen
dc.subjectSaltsen
dc.subjectCondensationen
dc.subjectProtonsen
dc.subjectHerz saltsen
dc.titleReaction of Herz salts with malononitrile: A general route to (6H-1,2,3-benzodithiazol-6-ylidene)malononitrilesen
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1039/b110024f
dc.description.volume3
dc.description.startingpage315
dc.description.endingpage319
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.description.notes<p>Cited By :12</p>en
dc.source.abbreviationJ Chem Soc Perkin Trans 1en
dc.contributor.orcidKoutentis, Panayiotis Andreas [0000-0002-4652-7567]
dc.gnosis.orcid0000-0002-4652-7567


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