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dc.contributor.authorHua, Guoxiong
dc.contributor.authorDu, Junyi
dc.contributor.authorSlawin, Alexandra Martha Zoya
dc.contributor.authorWoollins, John Derek
dc.date.accessioned2017-01-10T16:30:11Z
dc.date.available2017-01-10T16:30:11Z
dc.date.issued2016-12-29
dc.identifier248524993
dc.identifier2f01838a-2721-48d0-9d74-a373863fcb1e
dc.identifier85009811547
dc.identifier000395473500046
dc.identifier.citationHua , G , Du , J , Slawin , A M Z & Woollins , J D 2016 , ' Synthesis and single crystal structures of substituted-1,3-selenazol-2-amines ' , Molecules , vol. 22 , no. 1 , 46 . https://doi.org/10.3390/molecules22010046en
dc.identifier.issn1420-3049
dc.identifier.otherORCID: /0000-0002-9527-6418/work/56861733
dc.identifier.otherORCID: /0000-0002-1498-9652/work/31779151
dc.identifier.urihttps://hdl.handle.net/10023/10078
dc.descriptionThis article belongs to the Special Issue Celebrating Two Centuries of Research in Selenium Chemistry: State of the Art and New Prospectivesen
dc.description.abstractThe synthesis and X-ray single crystal structures of a series of new 4-substituted-1,3-selenazol-2-amines is reported. The efficient preparation of 4-substituted-1,3-selenazol-2-amines was carried out by two-component cyclization of the selenoureas with equi-molar amounts of α-haloketones. The selenoureas were obtained from the reaction of Woollins’ reagent with cyanamides, followed by hydrolysis with water. All new compounds have been characterized by IR spectroscopy, multi-NMR (1H, 13C, 77Se) spectroscopy, accurate mass measurement and single crystal X-ray structure analysis.
dc.format.extent1990265
dc.language.isoeng
dc.relation.ispartofMoleculesen
dc.subjectCyanamidesen
dc.subjectWoollins’ reagenten
dc.subjectSelenoureasen
dc.subjectSelenazol-2-aminesen
dc.subjectQD Chemistryen
dc.subjectDASen
dc.subject.lccQDen
dc.titleSynthesis and single crystal structures of substituted-1,3-selenazol-2-aminesen
dc.typeJournal articleen
dc.contributor.institutionUniversity of St Andrews. School of Chemistryen
dc.contributor.institutionUniversity of St Andrews. Office of the Principalen
dc.contributor.institutionUniversity of St Andrews. EaSTCHEMen
dc.identifier.doi10.3390/molecules22010046
dc.description.statusPeer revieweden
dc.identifier.urlhttp://www.mdpi.com/1420-3049/22/1/46/s1en


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