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2,6-exo-8,10-exo-4-Butyl-9-oxa-4-azatetracyclo[5.3.1.02,6.08,10]undecane-3,5-dione

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dc.contributor.authorAitken, R Alan
dc.contributor.authorFotherby, Fiona M.
dc.contributor.authorSlawin, Alexandra M. Z.
dc.date.accessioned2022-01-20T16:30:12Z
dc.date.available2022-01-20T16:30:12Z
dc.date.issued2022-01-20
dc.identifier277539245
dc.identifier83381fb0-f72b-4e28-826f-47c6069d62ac
dc.identifier85123519144
dc.identifier000774176400001
dc.identifier.citationAitken , R A , Fotherby , F M & Slawin , A M Z 2022 , ' 2,6- exo -8,10- exo -4-Butyl-9-oxa-4-azatetracyclo[5.3.1.0 2,6 .0 8,10 ]undecane-3,5-dione ' , Molbank , vol. 2022 , no. 1 , M1320 . https://doi.org/10.3390/M1320en
dc.identifier.issn1422-8599
dc.identifier.otherORCID: /0000-0002-9527-6418/work/106837951
dc.identifier.otherORCID: /0000-0001-6959-5311/work/106838052
dc.identifier.urihttps://hdl.handle.net/10023/24724
dc.description.abstractThe title epoxide was obtained by spontaneous epoxidation of the corresponding unsaturated imide in air or by peracid oxidation. Unambiguous assignment of the 1H and 13C NMR spectra is achieved by comparison between analogous compounds and its X-ray structure confirms the exo,exo-configuration.
dc.format.extent7
dc.format.extent1673666
dc.language.isoeng
dc.relation.ispartofMolbanken
dc.subjectEpoxideen
dc.subjectCyclic imideen
dc.subjectX-ray structureen
dc.subjectNMR assignmenten
dc.subjectQD Chemistryen
dc.subjectDASen
dc.subject.lccQDen
dc.title2,6-exo-8,10-exo-4-Butyl-9-oxa-4-azatetracyclo[5.3.1.02,6.08,10]undecane-3,5-dioneen
dc.typeJournal articleen
dc.contributor.institutionUniversity of St Andrews. EaSTCHEMen
dc.contributor.institutionUniversity of St Andrews. School of Chemistryen
dc.identifier.doihttps://doi.org/10.3390/M1320
dc.description.statusPeer revieweden


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