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dc.contributor.authorKonstantinova, Lidia S.
dc.contributor.authorKnyazeva, Ekaterina A.
dc.contributor.authorNefyodov, Andrey A.
dc.contributor.authorSanz Camacho, Paula
dc.contributor.authorAshbrook, Sharon Elizabeth
dc.contributor.authorWoollins, J Derek
dc.contributor.authorZibarev, Andrey V.
dc.contributor.authorRakitin, Oleg A.
dc.date.accessioned2016-01-21T00:12:20Z
dc.date.available2016-01-21T00:12:20Z
dc.date.issued2015-02
dc.identifier162445868
dc.identifier5a0b3ce4-f5bc-4272-8963-dd010e6ed382
dc.identifier84922571748
dc.identifier000350087800014
dc.identifier.citationKonstantinova , L S , Knyazeva , E A , Nefyodov , A A , Sanz Camacho , P , Ashbrook , S E , Woollins , J D , Zibarev , A V & Rakitin , O A 2015 , ' Direct synthesis of fused 1,2,5-selenadiazoles from 1,2,5-thiadiazoles ' , Tetrahedron , vol. 56 , no. 9 . https://doi.org/10.1016/j.tetlet.2015.01.106en
dc.identifier.issn0040-4020
dc.identifier.otherORCID: /0000-0002-4538-6782/work/56638974
dc.identifier.otherORCID: /0000-0002-1498-9652/work/31779186
dc.identifier.urihttps://hdl.handle.net/10023/8049
dc.descriptionThe authors acknowledge financial support from the Russian Foundation for Basic Research (Project 13-03-00072), from the Presidium of the Russian Academy of Sciences (Programme No. 8, Project 8.14) and from the Leverhulme Trust (Project IN-2012-094).en
dc.description.abstractA short and convenient synthesis of fused 1,2,5-selenadiazoles from corresponding 1,2,5-thiadiazoles and selenium dioxide has been developed.
dc.format.extent740864
dc.language.isoeng
dc.relation.ispartofTetrahedronen
dc.subjectSulfur-nitrogen heterocyclesen
dc.subjectFused 1,2,5-selenadiazolesen
dc.subject1,2,5-thiadiazolesen
dc.subjectSelenium dioxideen
dc.subjectQD Chemistryen
dc.subjectNDASen
dc.subject.lccQDen
dc.titleDirect synthesis of fused 1,2,5-selenadiazoles from 1,2,5-thiadiazolesen
dc.typeJournal articleen
dc.contributor.sponsorEPSRCen
dc.contributor.sponsorEPSRCen
dc.contributor.sponsorEPSRCen
dc.contributor.institutionUniversity of St Andrews. School of Chemistryen
dc.contributor.institutionUniversity of St Andrews. EaSTCHEMen
dc.contributor.institutionUniversity of St Andrews. Office of the Principalen
dc.identifier.doi10.1016/j.tetlet.2015.01.106
dc.description.statusPeer revieweden
dc.date.embargoedUntil2016-01-21
dc.identifier.grantnumberEP/K503940/1en
dc.identifier.grantnumberEP/K031252/1en
dc.identifier.grantnumberEP/K039210/1en


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