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      Raw data for new compounds described in the paper: "Enantioselective rhodium-catalyzed coupling of arylboronic acids, 1,3-enynes, and imines by alkenyl-to-allyl 1,4-rhodium(I) migration"

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      Raw Data for Enantioselective Rhodium-Catalyzed Coupling of Arylboronic Acids, 1,3-Enynes, and Imines.zip (88.70Mb)
      Publication date
      2017-10-10
      Creators
      Callingham, Michael
      Partridge, Benjamin M.
      Lewis, William
      Lam, Hon Wai
      Metadata
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      Description
      Raw data for new compounds described in the paper: "Enantioselective rhodium-catalyzed coupling of arylboronic acids, 1,3-enynes, and imines by alkenyl-to-allyl 1,4-rhodium(I) migration".
      External URI
      • https://rdmc.nottingham.ac.uk/handle/internal/334
      DOI
      • http://doi.org/10.17639/nott.330
      Related publication DOI
      • 10.1002/anie.201709334
      Subjects
      • Asymmetry (Chemistry)
      • Enantioselective catalysis
      • Imines
      • Isomerization
      • Rhodium
      • allylation, asymmetric catalysis, imine, isomerization, rhodium
      • Physical sciences::Chemistry::Organic chemistry
      • Q Science::QD Chemistry::QD241 Organic chemistry
      Divisions
      • University of Nottingham, UK Campus::Faculty of Science::School of Chemistry
      Deposit date
      2017-10-10
      Data type
      IR, NMR, mass spectrometry, and HPLC data
      Funders
      • Engineering & Physical Sciences Research Council
      • European Research Council
      • GlaxoSmithKline
      • The University of Nottingham
      Grant number
      • Starting Grant No. 258580
      • EP/I004769/1
      • EP/I004769/2
      Data collection method
      Using IR, NMR, and mass spectrometers, and HPLC machines
      Resource languages
      • en
      Publisher
      The University of Nottingham

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