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(S)-1-(Ethoxycarbonyl)ethyl (2R,5S)-2,5-Dimethyl-1,3-dioxolan-4-one-2-carboxylate

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dc.contributor.authorAitken, R Alan
dc.contributor.authorHaslett, Oliver E
dc.contributor.authorSlawin, Alexandra Martha Zoya
dc.date.accessioned2021-01-05T15:30:09Z
dc.date.available2021-01-05T15:30:09Z
dc.date.issued2021-01-02
dc.identifier.citationAitken , R A , Haslett , O E & Slawin , A M Z 2021 , ' ( S )-1-(Ethoxycarbonyl)ethyl (2 R ,5S)-2,5-Dimethyl-1,3-dioxolan-4-one-2-carboxylate ' , Molbank , vol. 2021 , no. 1 , M1178 . https://doi.org/10.3390/M1178en
dc.identifier.issn1422-8599
dc.identifier.otherPURE: 271870792
dc.identifier.otherPURE UUID: f8da2f90-c214-44f4-8ac8-e2a06b4c963d
dc.identifier.otherJisc: eafa01452c8c4efaba90d959a6683904
dc.identifier.otherORCID: /0000-0002-9527-6418/work/86537560
dc.identifier.otherORCID: /0000-0001-6959-5311/work/86538044
dc.identifier.otherJisc: eafa01452c8c4efaba90d959a6683904
dc.identifier.otherScopus: 85099402215
dc.identifier.otherWOS: 000633130000001
dc.identifier.urihttps://hdl.handle.net/10023/21222
dc.description.abstractThe title compound was obtained in low yield in the condensation of ethyl pyruvate and lactic acid. Its structure is determined by NMR methods and x-ray diffraction and the mechanism for formation of this 1:2 adduct from the initial 1:1 adduct is considered.
dc.format.extent4
dc.language.isoeng
dc.relation.ispartofMolbanken
dc.rightsCopyright © 2021 The Author(s). This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.en
dc.subject1,3-dioxolan-4-onesen
dc.subjectEthyl pyruvateen
dc.subjectLactic aciden
dc.subjectX-ray structureen
dc.subjectQD Chemistryen
dc.subjectDASen
dc.subject.lccQDen
dc.title(S)-1-(Ethoxycarbonyl)ethyl (2R,5S)-2,5-Dimethyl-1,3-dioxolan-4-one-2-carboxylateen
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/M1178
dc.description.statusPeer revieweden


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