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Synthesis of (R)-Lactic Acid and (2R,5R)-2-tert-Butyl-5-methyl-1,3-dioxolan-4-one

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dc.contributor.authorAitken, R Alan
dc.contributor.authorMeehan, Anna
dc.contributor.authorPower, Lynn Anita
dc.date.accessioned2016-04-01T23:01:12Z
dc.date.available2016-04-01T23:01:12Z
dc.date.issued2015-06-01
dc.identifier.citationAitken , R A , Meehan , A & Power , L A 2015 , ' Synthesis of (R)-Lactic Acid and (2R,5R)-2-tert-Butyl-5-methyl-1,3-dioxolan-4-one ' , Synthesis , vol. 47 , no. 11 , pp. 1557-1559 . https://doi.org/10.1055/s-0034-1380511en
dc.identifier.issn0039-7881
dc.identifier.otherPURE: 173098285
dc.identifier.otherPURE UUID: 56e03d16-4ca4-4678-9acd-db471d9aef8a
dc.identifier.otherScopus: 84929710588
dc.identifier.otherORCID: /0000-0001-6959-5311/work/34857577
dc.identifier.otherWOS: 000354769200005
dc.identifier.urihttps://hdl.handle.net/10023/8545
dc.description.abstractA convenient procedure for the synthesis of very expensive (R)-lactic acid from relatively inexpensive (R)-alanine is described. Its subsequent conversion into a chiral dioxolanone can be carried out by using an inexpensive pivalaldehyde–tert-butanol mixture.
dc.format.extent3
dc.language.isoeng
dc.relation.ispartofSynthesisen
dc.rights© Georg Thieme Verlag Stuttgart - New York. This work is made available online in accordance with the publisher’s policies. This is the author created, accepted version manuscript following peer review and may differ slightly from the final published version. The final published version of this work is available at http://dx.doi.org/10.1055/s-0034-1380511en
dc.subjectChiral poolen
dc.subjectStereoselective synthesisen
dc.subject(R)-lactic aciden
dc.subject(R)-alanineen
dc.subjectDiazotizationen
dc.subject1,3-dioxolan-4-oneen
dc.subjectQD Chemistryen
dc.subjectNDASen
dc.subject.lccQDen
dc.titleSynthesis of (R)-Lactic Acid and (2R,5R)-2-tert-Butyl-5-methyl-1,3-dioxolan-4-oneen
dc.typeJournal articleen
dc.description.versionPostprinten
dc.contributor.institutionUniversity of St Andrews. School of Chemistryen
dc.contributor.institutionUniversity of St Andrews. EaSTCHEMen
dc.identifier.doihttps://doi.org/10.1055/s-0034-1380511
dc.description.statusPeer revieweden
dc.date.embargoedUntil2016-04-02


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