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dc.contributor.authorKalogirou, Andreas S.en
dc.contributor.authorKoutentis, Panayiotis Andreasen
dc.creatorKalogirou, Andreas S.en
dc.creatorKoutentis, Panayiotis Andreasen
dc.date.accessioned2019-11-21T06:19:40Z
dc.date.available2019-11-21T06:19:40Z
dc.date.issued2016
dc.identifier.urihttp://gnosis.library.ucy.ac.cy/handle/7/55620
dc.source.urihttps://nls.ldls.org.uk/welcome.html?ark:/81055/vdc_100034090920.0x000025
dc.subjectChemistryen
dc.subjectOrganicen
dc.titleSubstitution chemistry of 3,5-dichloro-4H-1,2,6-thiadiazine 4,4-ketals[ONLINE]en
dc.typeinfo:eu-repo/semantics/article
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>ID: 1082en
dc.description.notesIn: Tetrahedron letters, Vol. 57, no. 30 ( 2016), p.3307-3310.en
dc.description.notesSummary: Graphical abstractHighlights•3,5-Dichloro-4H-1,2,6-thiadiazine 4,4-ketals undergo Pd-catalyzed C–C coupling at the C-3/5 positions.•Nucleophilic substitution at C-3/5 can occur with methoxide, phenoxide and pyrrolidine.•3,5-Diphenyl derivatives can be hydrolysed to 3,5-diphenyl-4H-1,2,6-thiadiazin-4-one.AbstractThe reactivity of 3,5-dichloro-4H-1,2,6-thiadiazine 4,4-ketals towards nucleophilic substitution or palladium-catalyzed C–C coupling at the C-3/5 positions led to seven new 3,5-disubstituted 4H-1,2,6-thiadiazine ethylene glycol 4,4-ketals and seven 3,5-disubstituted 4H-1,2,6-thiadiazine catechol 4,4-ketals in 83–98% yields. Furthermore, 3,5-diphenyl-4H-1,2,6-thiadiazine ethylene glycol and catechol 4,4-ketals were successfully hydrolysed in conc. H2SO4at 20 °C to afford 3,5-diphenyl-4H-1,2,6-thiadiazin-4-one in 74% and 89% yields.</p>en
dc.contributor.orcidKoutentis, Panayiotis Andreas [0000-0002-4652-7567]
dc.contributor.orcidKalogirou, Andreas S. [0000-0002-5476-5805]
dc.gnosis.orcid0000-0002-4652-7567
dc.gnosis.orcid0000-0002-5476-5805


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