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Synthesis and single crystal structures of N-substituted benzamides and their chemoselective selenation/reduction derivatives

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dc.contributor.authorHua, Guoxiong
dc.contributor.authorCarpenter-Warren, Cameron L.
dc.contributor.authorCordes, David B.
dc.contributor.authorSlawin, Alexandra M. Z.
dc.contributor.authorWoollins, J. Derek
dc.date.accessioned2021-04-19T11:30:14Z
dc.date.available2021-04-19T11:30:14Z
dc.date.issued2021-04-19
dc.identifier273832638
dc.identifier035ebdee-1f03-4a0f-8a44-5adf137df330
dc.identifier85105187341
dc.identifier000644622600001
dc.identifier.citationHua , G , Carpenter-Warren , C L , Cordes , D B , Slawin , A M Z & Woollins , J D 2021 , ' Synthesis and single crystal structures of N-substituted benzamides and their chemoselective selenation/reduction derivatives ' , Molecules , vol. 26 , no. 8 , 2367 . https://doi.org/10.3390/molecules26082367en
dc.identifier.issn1420-3049
dc.identifier.otherORCID: /0000-0002-9527-6418/work/92775146
dc.identifier.otherORCID: /0000-0002-1498-9652/work/92775154
dc.identifier.otherORCID: /0000-0002-5366-9168/work/92775164
dc.identifier.urihttps://hdl.handle.net/10023/23051
dc.description.abstractA series of N-aryl-N-(2-oxo-2-arylethyl) benzamides and cinnamides has been prepared. The reaction of the benzamides with Woollins’ reagent, a highly efficient chemoselective selenation/reduction reagent, gave the corresponding N-aryl-N-(arylenethyl) benzoselenoamides in good yields. Five representative single crystal X-ray structures are discussed.
dc.format.extent10
dc.format.extent727406
dc.language.isoeng
dc.relation.ispartofMoleculesen
dc.subjectN-substituted benzamidesen
dc.subjectWoollins’ reagenten
dc.subjectSelenation reagenten
dc.subjectReduction reagenten
dc.subjectSingle crystal X-ray structuresen
dc.subjectQD Chemistryen
dc.subjectDASen
dc.subject.lccQDen
dc.titleSynthesis and single crystal structures of N-substituted benzamides and their chemoselective selenation/reduction derivativesen
dc.typeJournal articleen
dc.contributor.institutionUniversity of St Andrews. School of Chemistryen
dc.contributor.institutionUniversity of St Andrews. EaSTCHEMen
dc.identifier.doihttps://doi.org/10.3390/molecules26082367
dc.description.statusPeer revieweden
dc.identifier.urlhttps://www.mdpi.com/journal/molecules/special_issues/Alexandra_Slawinen
dc.identifier.urlhttps://www.mdpi.com/1420-3049/26/8/2367en


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