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dc.contributor.authorBlake, Corrin
dc.contributor.authorChalmers, Brian A.
dc.contributor.authorClough, Lewis A.
dc.contributor.authorClunie, Dylan
dc.contributor.authorCordes, David B.
dc.contributor.authorLebl, Tomas
dc.contributor.authorMcDonald, Timothy R.
dc.contributor.authorSmith, Siobhan R.
dc.contributor.authorStuart-Morrison, Elliott
dc.contributor.authorSmellie, Iain A.
dc.date.accessioned2022-08-29T11:30:17Z
dc.date.available2022-08-29T11:30:17Z
dc.date.issued2022-08-28
dc.identifier281074884
dc.identifierd2abec41-47ce-4d3a-9dd7-7cb69e877802
dc.identifier000858759700001
dc.identifier85138602351
dc.identifier.citationBlake , C , Chalmers , B A , Clough , L A , Clunie , D , Cordes , D B , Lebl , T , McDonald , T R , Smith , S R , Stuart-Morrison , E & Smellie , I A 2022 , ' (9R,9aS,12aR,13S)-9,13-Diphenyl-9,9a,12a,13-tetrahydro-9,13-methanotriphenyleno[2,3-c]furan-10,12,14-trione ' , Molbank , vol. 2022 , no. 3 , M1435 . https://doi.org/10.3390/M1435en
dc.identifier.issn1422-8599
dc.identifier.otherBibtex: M1435
dc.identifier.otherORCID: /0000-0002-2999-2272/work/118411713
dc.identifier.otherORCID: /0000-0002-0269-3221/work/118411862
dc.identifier.otherORCID: /0000-0002-5366-9168/work/118411870
dc.identifier.otherORCID: /0000-0002-5829-6487/work/127066312
dc.identifier.urihttps://hdl.handle.net/10023/25905
dc.description.abstractX-ray crystallography was used to characterise the title compound for the first time, and the 1H NMR, 13C NMR and IR spectroscopic data from earlier reports were also updated.
dc.format.extent6
dc.format.extent1704310
dc.language.isoeng
dc.relation.ispartofMolbanken
dc.subjectX-ray structureen
dc.subjectInclusion compoundsen
dc.subjectNRM spectraen
dc.subjectIR spectrumen
dc.subjectQD Chemistryen
dc.subjectDASen
dc.subjectMCCen
dc.subject.lccQDen
dc.title(9R,9aS,12aR,13S)-9,13-Diphenyl-9,9a,12a,13-tetrahydro-9,13-methanotriphenyleno[2,3-c]furan-10,12,14-trioneen
dc.typeJournal articleen
dc.contributor.institutionUniversity of St Andrews. School of Chemistryen
dc.contributor.institutionUniversity of St Andrews. EaSTCHEMen
dc.identifier.doi10.3390/M1435
dc.description.statusPeer revieweden


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