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dc.contributor.authorFuentes García, José Antonio
dc.contributor.authorPittaway, Rachael
dc.contributor.authorClarke, Matt
dc.date.accessioned2015-07-08T16:10:10Z
dc.date.available2015-07-08T16:10:10Z
dc.date.issued2015-07-14
dc.identifier192606476
dc.identifiercf330912-f31a-4591-87f4-0fbcf992cdcc
dc.identifier84936990203
dc.identifier000357984900007
dc.identifier.citationFuentes García , J A , Pittaway , R & Clarke , M 2015 , ' Rapid asymmetric transfer hydroformylation (ATHF) of disubstituted alkenes using paraformaldehyde as a syngas surrogate ' , Chemistry - A European Journal , vol. 21 , no. 30 , pp. 10645-10649 . https://doi.org/10.1002/chem.201502049en
dc.identifier.issn0947-6539
dc.identifier.otherORCID: /0000-0002-2444-1244/work/59464621
dc.identifier.urihttps://hdl.handle.net/10023/6939
dc.descriptionThe authors thank Dr. Reddys (UK) and the Royal Society for an Industry Fellowship in the early stage of this work (2012–2014), and the EPSRC for funding (EP/M003868/1).en
dc.description.abstractAs an alternative to conventional asymmetric hydroformylation (AHF), Asymmetric Transfer Hydroformylation (ATHF) using formaldehyde as a surrogate for syngas is reported. A catalyst derived from commercially available [Rh(acac)(CO)2] and Ph-BPE stands out in terms of both activity and enantioselectivity. Remarkably, not only are high selectivities achievable, the reactions are very simple to carry out, and can give higher enantioselectivity (up to 96% e.e.) and/or turnover frequencies than those that are achievable using the same catalyst (or other leading catalysts) using typical conditions for AHF.
dc.format.extent295228
dc.language.isoeng
dc.relation.ispartofChemistry - A European Journalen
dc.subjectEnantioselective Catalysisen
dc.subjectMicrowaveen
dc.subjectCarbinylationen
dc.subjectHydroformylationen
dc.subjectFormaldehydeen
dc.subjectQD Chemistryen
dc.subjectNDASen
dc.subjectBDCen
dc.subject.lccQDen
dc.titleRapid asymmetric transfer hydroformylation (ATHF) of disubstituted alkenes using paraformaldehyde as a syngas surrogateen
dc.typeJournal articleen
dc.contributor.sponsorThe Royal Societyen
dc.contributor.sponsorEPSRCen
dc.contributor.institutionUniversity of St Andrews. School of Chemistryen
dc.contributor.institutionUniversity of St Andrews. EaSTCHEMen
dc.identifier.doihttps://doi.org/10.1002/chem.201502049
dc.description.statusPeer revieweden
dc.identifier.grantnumberIF120023en
dc.identifier.grantnumberEP/M003868/1en


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