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Reaction of tetracyanoethylene with SCL2: New molecular rearrangements

dc.contributor.authorKoutentis, Panayiotis Andreasen
dc.contributor.authorRees, C. W.en
dc.contributor.authorWhite, A. J. P.en
dc.contributor.authorWilliams, D. J.en
dc.creatorKoutentis, Panayiotis Andreasen
dc.creatorRees, C. W.en
dc.creatorWhite, A. J. P.en
dc.creatorWilliams, D. J.en
dc.date.accessioned2019-11-21T06:20:56Z
dc.date.available2019-11-21T06:20:56Z
dc.date.issued2000
dc.identifier.issn1359-7345
dc.identifier.urihttp://gnosis.library.ucy.ac.cy/handle/7/55738
dc.description.abstractThe chloride ion catalysed addition of SCl2 to TCNE gives the dicyanomethylene-1,2,6-thiadiazine 3 as major product together with two unexpected minor products, pyrimidine 4 and pyrroloimidazothiadiazine 5, whose X-ray crystal structures are describeden
dc.description.abstractthe products are derived from interaction of SCl2 with one cyano group with neighbouring group participation by two others.en
dc.sourceChemical Communicationsen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-0034696114&partnerID=40&md5=5495a36abda2a430b8f5a35f3d6505c3
dc.subjectarticleen
dc.subjectmolecular interactionen
dc.subjectcrystal structureen
dc.subjectX ray crystallographyen
dc.subjectsulfur derivativeen
dc.subjectchemical reactionen
dc.subjectreaction analysisen
dc.subjectchlorine derivativeen
dc.subjecttetracyanoethyleneen
dc.subjectthiadiazine derivativeen
dc.subjectderivatizationen
dc.subjectpyrimidine derivativeen
dc.titleReaction of tetracyanoethylene with SCL2: New molecular rearrangementsen
dc.typeinfo:eu-repo/semantics/article
dc.description.issue4
dc.description.startingpage303
dc.description.endingpage304
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.source.abbreviationChem.Commun.en
dc.contributor.orcidKoutentis, Panayiotis Andreas [0000-0002-4652-7567]
dc.gnosis.orcid0000-0002-4652-7567


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