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dc.contributor.authorAitken, R Alan
dc.contributor.authorPower, Lynn Anita
dc.contributor.authorSlawin, Alexandra Martha Zoya
dc.date.accessioned2023-07-20T09:30:07Z
dc.date.available2023-07-20T09:30:07Z
dc.date.issued2023-07-20
dc.identifier290658470
dc.identifierf437ed91-8061-4462-93d2-d7b3d4454550
dc.identifier85172774563
dc.identifier.citationAitken , R A , Power , L A & Slawin , A M Z 2023 , ' (2 S ,2' S ,4 R ,5 S ,5' R )-2,2'-Di- tert -butyl-4-hydroxy-5,5'-dimethyl-4,5'-bi(1,3-dioxolanyl)-4'-one ' , Molbank , vol. 2023 , no. 3 , M1699 . https://doi.org/10.3390/M1699en
dc.identifier.issn1422-8599
dc.identifier.otherORCID: /0000-0001-6959-5311/work/139156616
dc.identifier.otherORCID: /0000-0002-9527-6418/work/139156654
dc.identifier.urihttps://hdl.handle.net/10023/27992
dc.descriptionFunding: The authors thank the School of Chemistry for a studentship to L.A.P.en
dc.description.abstractThe product formed by base-induced dimerisation of (2S,5S)-2-tert-butyl-5-methyl-1,3-dioxolan-4-one is shown by X-ray diffraction to be the title compound and not the isomeric fused-ring 1,3-dioxolane/1,3-dioxane-4-one structure proposed by previous workers. The analogous compound derived from (2S,5S)-5-benzyl-2-tert-butyl-1,3-dioxolan-4-one has also been obtained and characterised.
dc.format.extent5
dc.format.extent1512186
dc.language.isoeng
dc.relation.ispartofMolbanken
dc.subjectX-ray structureen
dc.subjectStructural revisionen
dc.subjectHydrogen bondingen
dc.subject1,3-dioxolan-4-oneen
dc.subjectQD Chemistryen
dc.subjectDASen
dc.subjectMCCen
dc.subject.lccQDen
dc.title(2S,2'S,4R,5S,5'R)-2,2'-Di-tert-butyl-4-hydroxy-5,5'-dimethyl-4,5'-bi(1,3-dioxolanyl)-4'-oneen
dc.typeJournal articleen
dc.contributor.institutionUniversity of St Andrews. EaSTCHEMen
dc.contributor.institutionUniversity of St Andrews. School of Chemistryen
dc.identifier.doi10.3390/M1699
dc.description.statusPeer revieweden


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