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dc.contributor.authorWidegren, Magnus B.
dc.contributor.authorClarke, Matthew L.
dc.date.accessioned2019-04-18T23:38:08Z
dc.date.available2019-04-18T23:38:08Z
dc.date.issued2018-05-04
dc.identifier252805467
dc.identifier2477b1bf-1f16-4f5f-938c-4adc5e57c9e9
dc.identifier85046677522
dc.identifier000431726900036
dc.identifier.citationWidegren , M B & Clarke , M L 2018 , ' Manganese catalyzed hydrogenation of enantiomerically pure esters ' , Organic Letters , vol. 20 , no. 9 , pp. 2654-2658 . https://doi.org/10.1021/acs.orglett.8b00864en
dc.identifier.issn1523-7060
dc.identifier.otherORCID: /0000-0002-2444-1244/work/62668378
dc.identifier.urihttps://hdl.handle.net/10023/17545
dc.descriptionThe authors thank the EPSRC for DTG funding for MBW. The technical support staff at St Andrews are also gratefully acknowledged. The research data supporting this publication can be accessed at: dx.doi.org/10.17630/29308cf7-b6b6- 4b1b-809b-a12fe91b250fen
dc.description.abstractA manganese-catalyzed hydrogenation of esters has been accomplished with TON up to 1000, using cheap, environmentally benign, potassium carbonate and simple alcohols as activator and solvent, respectively. The weakly basic conditions lead to good functional group tolerance and enable the hydrogenation of enantiomerically enriched α-chiral esters with essentially no loss of stereochemical integrity.
dc.format.extent5
dc.format.extent510270
dc.language.isoeng
dc.relation.ispartofOrganic Lettersen
dc.subjectQD Chemistryen
dc.subjectDASen
dc.subject.lccQDen
dc.titleManganese catalyzed hydrogenation of enantiomerically pure estersen
dc.typeJournal articleen
dc.contributor.institutionUniversity of St Andrews. School of Chemistryen
dc.contributor.institutionUniversity of St Andrews. EaSTCHEMen
dc.identifier.doi10.1021/acs.orglett.8b00864
dc.description.statusPeer revieweden
dc.date.embargoedUntil2019-04-19


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