Search results

  • Full text

  • Document type

  • Organisation

Results: 8
Number of items: 8
  • Sinha, V., Bai, S., Kluwer, A. M., Reek, J., Linnebank, P., Lutz, M., De Bruin, B., Abiri, Z., & Dydio, P. (2019). CCDC 1877078: Experimental Crystal Structure Determination [Data set]. The Cambridge Structural Database. https://doi.org/10.5517/ccdc.csd.cc2107x7
  • Linnebank, P., Abiri, Z., de Bruin, B., Sinha, V., Lutz, M., Dydio, P., Reek, J., Kluwer, A. M., & Bai, S. (2019). CCDC 1877079: Experimental Crystal Structure Determination [Data set]. The Cambridge Structural Database. https://doi.org/10.5517/ccdc.csd.cc2107y8
  • Open Access
    Bai, S.-T., Bheeter, C. B., & Reek, J. N. H. (2019). Hydrogen Bond Directed ortho-Selective C-H Borylation of Secondary Aromatic Amides. Angewandte Chemie, International Edition, 58(37), 13039-13043. https://doi.org/10.1002/anie.201907366, https://doi.org/10.1002/ange.201907366
  • Open Access
    Bai, S.-T., Sinha, V., Kluwer, A. M., Linnebank, P. R., Abiri, Z., de Bruin, B., & Reek, J. N. H. (2019). Rational Redesign of a Regioselective Hydroformylation Catalyst for 3-Butenoic Acid by Supramolecular Substrate Orientation. ChemCatChem, 11(21), 5322-5329. https://doi.org/10.1002/cctc.201900487
  • Open Access
    Bai, S.-T., Sinha, V., Kluwer, A. M., Linnebank, P. R., Abiri, Z., Dydio, P., Lutz, M., de Bruin, B., & Reek, J. N. H. (2019). Effector responsive hydroformylation catalysis. Chemical Science, 10(31), 7389-7398. https://doi.org/10.1039/c9sc02558h
  • Open Access
    Bai, S.-T., Kluwer, A. M., & Reek, J. N. H. (2019). Effector enhanced enantioselective hydroformylation. Chemical Communications, 55(94), 14151-14154. https://doi.org/10.1039/c9cc07327b
  • Open Access
    Bai, S.-T., Bheeter, C. B., & Reek, J. N. H. (2019). Hydrogen Bond Directed ortho-Selective C-H Borylation of Secondary Aromatic Amides. Angewandte Chemie, 131(37), 13173-13177. https://doi.org/10.1002/ange.201907366, https://doi.org/10.1002/anie.201907366
  • Open Access
    Bai, S. (2019). Supramolecular transition metal catalysis: Effector controlled catalysis and supramolecular substrate preorganization. [Thesis, fully internal, Universiteit van Amsterdam].
Page of