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dc.contributor.authorAitken, R Alan
dc.contributor.authorFotherby, Fiona M.
dc.contributor.authorSlawin, Alexandra M. Z.
dc.date.accessioned2020-04-03T08:30:01Z
dc.date.available2020-04-03T08:30:01Z
dc.date.issued2020-04-02
dc.identifier.citationAitken , R A , Fotherby , F M & Slawin , A M Z 2020 , ' 2,6-­ exo -­8,12-­ exo -­10-­Butyl-­13-­oxa-­3,5-­dithia-10-azatetracyclo[5.5.1.0 2,6 .0 8,12 ]tridecane-­9,11-­dione ' , Molbank , vol. 2020 , no. 2 , M1123 . https://doi.org/10.3390/M1123en
dc.identifier.issn1422-8599
dc.identifier.otherPURE: 267149017
dc.identifier.otherPURE UUID: 724e76d3-b341-4c44-8a6e-b604839ea40d
dc.identifier.otherORCID: /0000-0002-9527-6418/work/71559612
dc.identifier.otherORCID: /0000-0001-6959-5311/work/71559858
dc.identifier.otherScopus: 85083783056
dc.identifier.otherWOS: 000551575100011
dc.identifier.urihttps://hdl.handle.net/10023/19750
dc.description.abstractThe title compound was obtained in low yield and spectroscopically characterised. Its x-­ray structure was compared with those of other crystallographically characterised 2-­unsubstituted 1,3-­dithiolanes.
dc.format.extent7
dc.language.isoeng
dc.relation.ispartofMolbanken
dc.rightsCopyright © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).en
dc.subject1,3-­dithiolaneen
dc.subjectCyclic imideen
dc.subjectx-­ray structureen
dc.subjectEnvelope conformationen
dc.subjectQD Chemistryen
dc.subjectDASen
dc.subject.lccQDen
dc.title2,6-­exo-­8,12-­exo-­10-­Butyl-­13-­oxa-­3,5-­dithia-10-azatetracyclo[5.5.1.02,6.08,12]tridecane-­9,11-­dioneen
dc.typeJournal articleen
dc.description.versionPublisher PDFen
dc.contributor.institutionUniversity of St Andrews. EaSTCHEMen
dc.contributor.institutionUniversity of St Andrews. School of Chemistryen
dc.identifier.doihttps://doi.org/10.3390/M1123
dc.description.statusPeer revieweden


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