 | Ricardo Meyrelles University of Vienna Institute of Theoretical Chemistry Währinger Str. 17 1090 Vienna Austria ricardo.meyrelles@univie.ac.at +43 1 4277 52763 ORCID: 0000-0002-0976-5494 |
| Publications |
Mechanistic Study on Selenium- and Sulfur-mediated Isomerisation of Hydroxamic Acids Chem. Eur. J., (accepted), (2023) 11. P. Spieß, A. Sirvent, I. Tiefenbrunner, J. Sargueil, A. J. Fernandes, A. Arroyo-Bondía, R. Meyrelles, D. Just, A. Prado-Roller, S. Shaaban, D. Kaiser, N. Maulide Nms-sulfonamide: a New Amine Protecting Group enables Unique Stability and Selectivity Chem. Eur. J. 29, e202301312, (2023), DOI: 10.1002/chem.202301312 10. M. Feng, A. J. Fernandes, R. Meyrelles, N. Maulide Direct Enantioselective α-Amination of Amides Guided by DFT Prediction of E/Z Selectivity in a Sulfonium Intermediate Chem , , (2023), DOI: 10.1016/j.chempr.2023.03.002 9. P. S. Grant, R. Meyrelles, O. Gajsek, G. Niederacher, B. Maryasin, N. Maulide Biomimetic Cationic Cyclopropanation Enables an Efficient Chemoenzymatic Synthesis of 6,8-Cycloeudesmanes J. Am. Chem. Soc. 145, 5855–5863, (2023), DOI: 10.1021/jacs.2c13116 8. M. Feng, R. Tinelli, R. Meyrelles, L. González, B. Maryasin, N. Maulide Direct Synthesis of α-Amino Acid Derivatives via Hydrative Amination of Alkynes Angew. Chem. Int. Ed. 62, e202212399, (2022), DOI: 10.1002/anie.202212399 7. J. Merad, P. Grant, T. Stopka, J. Sabbatani, R. Meyrelles, A. Preinfalk, J. Matyasovsky, B. Maryasin, L. González, N. Maulide Direct Stereodivergent Olefination of Carbonyl Compounds with Sulfur Ylides J. Am. Chem. Soc. 144, 12536–12543, (2022), DOI: 10.1021/jacs.2c05637 6. M. Lemmerer, M. Riomet, R. Meyrelles, B. Maryasin, L. González, N. Maulide HFIP Mediates a Direct C-C Coupling Between Michael Acceptors and Eschenmoser's Salt Angew. Chem. Int. Ed. 61, e202109933, (2022), DOI: 10.1002/anie.202109933 M. Lemmerer, M. Riomet, R. Meyrelles, B. Maryasin, L. González, N. Maulide Computational Investigation of the Aza-Cope Rearrangement Leading to Angularly Substituted 1-Azabicyclic Rings Synlett , , (2022), DOI: 10.1055/a-1946-6578 4. H. Chuang, M. Schupp, R. Meyrelles, B. Maryasin, N. Maulide Redox-Neutral Selenium-Catalysed Isomerisation of para-Hydroxamic Acids into para-Aminophenols Angew. Chem. 60, 13778-13782, (2021), DOI: 10.1002/anie.202100801 Cover Image: H. Chuang, M. Schupp, R. Meyrelles, B. Maryasin, N. Maulide Immobilization of His-Tagged Proteins on NiO Foams for Recyclable Enzymatic Reactors Appl. Sur. Sci. 537, 147848, (2021), DOI: 10.1016/j.apsusc.2020.147848 2. R. Oost, J. D. Neuhaus, A. Misale, R. Meyrelles, L. F. Veiros, N. Maulide Catalyst-Dependent Selectivity in Sulfonium Ylide Cycloisomerization Reactions Chem. Sci. 9, 7091-7095, (2018), DOI: 10.1039/C8SC02815J 1. S. Hazra, R. Meyrelles,A. J. Charmier, P. Rijo, M. F. C. G. Silva, A. J. L. Pombeiro N–H⋯O and N–H⋯Cl Supported 1D Chains of Heterobimetallic CuII/NiII–SnIV Cocrystals Dalton Trans. 45, 17929-17938, (2016), DOI: 10.1039/C6DT03118H |