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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.identifier271870792
dc.identifierf8da2f90-c214-44f4-8ac8-e2a06b4c963d
dc.identifier85099402215
dc.identifier000633130000001
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.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.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.format.extent1895691
dc.language.isoeng
dc.relation.ispartofMolbanken
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.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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