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dc.contributor.authorPoh, Jian Siangen
dc.contributor.authorGreb, Aen
dc.contributor.authorGreed, Sen
dc.contributor.authorBattilocchio, Claudioen
dc.contributor.authorPasau, Pen
dc.contributor.authorBlakemore, DCen
dc.contributor.authorLey, Stevenen
dc.date.accessioned2017-09-11T11:31:34Z
dc.date.available2017-09-11T11:31:34Z
dc.identifier.urihttps://www.repository.cam.ac.uk/handle/1810/267128
dc.descriptionThis data contains a .zip file of the NMR spectra for the compounds (in .mnova format, to be opened in MestReNova) described in the Supplementary Information. It also contains a .pdf copy of the Supplementary Information, which contains the experimental details and full characterisation data (NMR, IR, HRMS) of all compounds produced in this publication. A .xlsx file is provided which contains the raw FlowIR data for showing the presence of the reactive intermediate, 4-diazotetrahydropyran.en
dc.description.sponsorshipCambridge Home and European Scholarship Scheme, UCB Biopharma SPRL, Pfizer.en
dc.formatWinZip, MestReNova, Adobe Reader, Microsoft Excelen
dc.rightsAttribution 4.0 Internationalen
dc.rightsAttribution 4.0 Internationalen
dc.rightsAttribution 4.0 Internationalen
dc.rightsAttribution 4.0 Internationalen
dc.rightsAttribution 4.0 Internationalen
dc.rightsAttribution 4.0 Internationalen
dc.rightsAttribution 4.0 Internationalen
dc.rightsAttribution 4.0 Internationalen
dc.rightsAttribution 4.0 Internationalen
dc.rightsAttribution 4.0 Internationalen
dc.rightsAttribution 4.0 Internationalen
dc.rightsAttribution 4.0 Internationalen
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en
dc.subjectFlow chemistryen
dc.subjectDiazo compoundsen
dc.subjectCross-couplingen
dc.subjectBoronic acidsen
dc.subjectPhotochemistryen
dc.titleResearch data supporting 'A New Versatile Route to Unstable Diazo Compounds via Oxadiazolines and Use In Aryl-Alkyl Cross-Coupling Reactions'en
dc.typeDataset
dc.identifier.doi10.17863/CAM.12635
rioxxterms.licenseref.urihttp://creativecommons.org/licenses/by/4.0/en
datacite.contributor.supervisorLey, Steven Victor
dcterms.formatzip, mnova, pdf, xlsxen
dc.contributor.orcidBattilocchio, Claudio [0000-0002-4601-8527]
dc.contributor.orcidLey, Steven [0000-0002-7816-0042]
rioxxterms.typeOtheren
pubs.funder-project-idEPSRC (EP/K009494/1)
pubs.funder-project-idEPSRC (EP/M004120/1)
pubs.funder-project-idEPSRC (EP/K039520/1)
datacite.issupplementto.doi10.1002/anie.201710445en


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Attribution 4.0 International
Except where otherwise noted, this item's licence is described as Attribution 4.0 International