Publications

ZORA Publication List

Publications

• 2017

  • Journal Article

    • García-Domínguez, A., Li, Z., & Nevado, C. (2017). Nickel-catalyzed reductive dicarbofunctionalization of alkenes Journal of the American Chemical Society, 139, 6835–6838. https://doi.org/10.1021/jacs.7b03195

• 2016

  • Journal Article

    • Hofer, M., Genoux, A., Kumar, R., & Nevado, C. (2016). Gold-catalyzed direct oxidative arylation with boron coupling partners Angewandte Chemie Internationale Edition, 56, 1021–1025. https://doi.org/10.1002/anie.201610457
    • Kumar, R., Linden, A., & Nevado, C. (2016). Evidence for direct transmetalation of AuIII–F with boronic acids Journal of the American Chemical Society, 138, 13790–13793. https://doi.org/10.1021/jacs.6b07763
    • Felker, A., Nieuwenhuize, S., Dolbois, A., Blazkova, K., Hess, C., Low, L. W. L., Burger, S., Samson, N., Carney, T. J., Bartunek, P., Nevado, C., & Mosimann, C. (2016). In vivo performance and properties of tamoxifen metabolites for CreERT2 control PLoS ONE, 11, e0152989. https://doi.org/10.1371/journal.pone.0152989
    • Unzue, A., Lafleur, K., Zhao, H., Zhou, T., Dong, J., Kolb, P., Liebl, J., Zahler, S., Caflisch, A., & Nevado, C. (2016). Three stories on Eph kinase inhibitors: From in silico discovery to in vivo validation European Journal of Medicinal Chemistry, 112, 347–366. https://doi.org/10.1016/j.ejmech.2016.01.057
    • Unzue, A., Xu, M., Dong, J., Wiedmer, L., Spiliotopoulos, D., Caflisch, A., & Nevado, C. (2016). Fragment-based design of selective nanomolar ligands of the crebbp bromodomain Journal of Medicinal Chemistry, 59, 1350–1356. https://doi.org/10.1021/acs.jmedchem.5b00172
    • Unzue, A., Zhao, H., Lolli, G., Dong, J., Zhu, J., Zechner, M., Dolbois, A., Caflisch, A., & Nevado, C. (2016). The “Gatekeeper” residue influences the mode of binding of acetyl indoles to bromodomains Journal of Medicinal Chemistry, 59, 3087–3097. https://doi.org/10.1021/acs.jmedchem.5b01757
    • García-Domínguez, P., Fehr, L., Rusconi, G., & Nevado, C. (2016). Palladium-catalyzed incorporation of atmospheric CO2: efficient synthesis of functionalized oxazolidinones Chemical Science, 7, 3914–3918. https://doi.org/10.1039/C6SC00419A
    • García-Domínguez, P., & Nevado, C. (2016). Au–Pd bimetallic catalysis: the importance of anionic ligands in catalyst speciation Journal of the American Chemical Society, 138, 3266–3269. https://doi.org/10.1021/jacs.5b10277

• 2015

  • Journal Article

    • Kong, W., Fuentes, N., García-Domínguez, A., Merino, E., & Nevado, C. (2015). Stereoselective synthesis of highly functionalized indanes and dibenzocycloheptadienes through complex radical cascade reactions Angewandte Chemie Internationale Edition, 54, 2487–2491. https://doi.org/10.1002/anie.201409659
    • Kumar, R., Linden, A., & Nevado, C. (2015). Luminescent (N^C^C)-Gold(III) Complexes: Stabilized Gold(III) fluorides Angewandte Chemie Internationale Edition, 54, 14287–14290. https://doi.org/10.1002/anie.201505533
    • Xu, M., Unzue, A., Dong, J., Spiliotopoulos, D., Nevado, C., & Caflisch, A. (2015). Discovery of CREBBP bromodomain inhibitors by high-throughput docking and hit optimization guided by molecular dynamics Journal of Medicinal Chemistry, 2487–2491. https://doi.org/10.1021/acs.jmedchem.5b00171
    • Fuentes, N., Kong, W., Fernández-Sánchez, L., Merino, E., & Nevado, C. (2015). Cyclization cascades via N-amidyl radicals toward highly functionalized heterocyclic scaffolds Journal of the American Chemical Society, 137, 964–973. https://doi.org/10.1021/ja5115858
    • Li, Z., García-Domínguez, A., & Nevado, C. (2015). Pd-catalyzed stereoselective carboperfluoroalkylation of alkynes Journal of the American Chemical Society, 137, 11610–11613. https://doi.org/10.1021/jacs.5b07432

• 2014

  • Journal Article

    • Kong, W., Merino, E., & Nevado, C. (2014). Arylphosphonylation and Arylazidation of Activated Alkenes Angewandte Chemie Internationale Edition, 53, 5078–5082. https://doi.org/10.1002/anie.201311241
    • Merino, E., & Nevado, C. (2014). Addition of CF$_3$ across unsaturated moieties: a powerful functionalization tool Chemical Society Reviews, 43, 6598–6608. https://doi.org/10.1039/c4cs00025k
    • Unzue, A., Dong, J., Lafleur, K., Zhao, H., Frugier, E., Caflisch, A., & Nevado, C. (2014). Pyrrolo[3,2-b]quinoxaline derivatives as types I1/2 and II Eph tyrosine kinase inhibitors: structure-based design, synthesis, and in vivo validation Journal of Medicinal Chemistry, 57, 6834–6844. https://doi.org/10.1021/jm5009242
    • Kong, W., Merino, E., & Nevado, C. (2014). Divergent reaction mechanisms in the aminofluorination of alkenes Chimia, 68, 430–435. https://doi.org/10.2533/chimia.2014.430

  • Book Section

    • Merino, E., Fernandez, L., & Nevado, C. (2014). Gold‐Catalyzed Migrations and Ring Expansions In Z. Rappoport, J. F. Liebman, & I. Marek (Eds.), Patai’s Chemistry of functional groups (pp. 1–72). https://doi.org/10.1002/9780470682531.pat0811

• 2013

  • Journal Article

    • Kong, W., Casimiro, M., Fuentes, N., Merino, E., & Nevado, C. (2013). Metal-free aryltrifluoromethylation of activated alkenes Angewandte Chemie Internationale Edition, 52, 13086–13090. https://doi.org/10.1002/anie.201307377
    • Kong, W., Casimiro, M., Merino, E., & Nevado, C. (2013). Copper-catalyzed one-pot trifluoromethylation/aryl migration/desulfonylation and C(sp2)-N bond formation of conjugated tosyl amides Journal of the American Chemical Society, 135, 14480–14483. https://doi.org/10.1021/ja403954g
    • Lafleur, K., Dong, J., Huang, D., Caflisch, A., & Nevado, C. (2013). Optimization of inhibitors of the tyrosine kinase EphB4. 2. Cellular potency improvement and binding mode validation by X-ray crystallography Journal of Medicinal Chemistry, 56, 84–96. https://doi.org/10.1021/jm301187e
    • Merino, E., & Nevado, C. (2013). On gold catalysis and beyond Chimia, 67, 663–668. https://doi.org/10.2533/chimia.2013.663

• 2008

  • Journal Article

    • Zou, Y., Garayalde, D., Wang, Q., Nevado, C., & Goeke, A. (2008). Gold-catalyzed cycloisomerization of cyclopropyl alkynyl acetates: a versatile approach to 5-, 6-, and 7-membered carbocycles Angewandte Chemie Internationale Edition, 47, 10110–10113. https://doi.org/10.1002/anie.200804202

Pagination