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dc.contributor.authorShi, Yiping
dc.contributor.authorKamer, Paulus Clemens Jozef
dc.contributor.authorCole-Hamilton, David John
dc.date.accessioned2018-10-10T23:48:44Z
dc.date.available2018-10-10T23:48:44Z
dc.date.issued2017-10-11
dc.identifier251540503
dc.identifier89e6d829-5c62-410d-8ef9-3d88934c22be
dc.identifier85034236508
dc.identifier000415115600020
dc.identifier.citationShi , Y , Kamer , P C J & Cole-Hamilton , D J 2017 , ' A new route to α,ω-diamines from hydrogenation of dicarboxylic acids and their derivatives in the presence of amines ' , Green Chemistry , vol. 19 , pp. 5460-5466 . https://doi.org/10.1039/C7GC02838Een
dc.identifier.issn1463-9262
dc.identifier.urihttps://hdl.handle.net/10023/16186
dc.descriptionWe thank the EPSRC for the critical mass grant 'Clean Catalysis for Sustainable Development' (EP/J018139/1), Sasol Technology, UK for a case studentship (Y. S.) and the EPSRC UK National Mass Spectrometry Facility at Swansea University for mass spectrometric analysisen
dc.description.abstractA new and selective route for the synthesis of polymer precursors, primary diamines or N-substituted diamines, from dicarboxylic acids, diesters, diamides and diols using a Ru/ triphos catalyst is reported. Excellent conversions and yields are obtained under optimised reaction conditions. The reactions worked very well using 1,4-dioxane as solvent, but the greener solvent, 2-methyl tetrahydrofuran, also gave very similar results. This method provides a potential route to converting waste biomass to value added materials. The reaction is proposed to go through both amide and aldehyde pathways.
dc.format.extent660294
dc.language.isoeng
dc.relation.ispartofGreen Chemistryen
dc.subjectQD Chemistryen
dc.subjectNDASen
dc.subject.lccQDen
dc.titleA new route to α,ω-diamines from hydrogenation of dicarboxylic acids and their derivatives in the presence of aminesen
dc.typeJournal articleen
dc.contributor.sponsorEPSRCen
dc.contributor.institutionUniversity of St Andrews. School of Chemistryen
dc.contributor.institutionUniversity of St Andrews. EaSTCHEMen
dc.identifier.doi10.1039/C7GC02838E
dc.description.statusPeer revieweden
dc.date.embargoedUntil2018-10-11
dc.identifier.grantnumberEP/J018139/1en


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