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 |
Diastereoselective Umpolung Cyclisation of Ketones Promoted by Hypervalent Iodine (submitted), (2024) 18. K. Song, R. Meyrelles, G. Pilet, B. Maryasin, M. Médebielle, J. Merad Dication Disulfuranes as Photoactivatable Sources of Radical Organocatalysts Angew. Chem. Int. Ed. , (accepted), (2024) 17. P. S. Grant, M. Vavrík, V. Porte, R. Meyrelles, N. Maulide Remote Proton Elimination: C–H Activation Enabled by Distal Acidification Science 384, 815-820, (2024), DOI: 10.1126/science.adi8997 16. P. Spiess, J. Brześkiewicz, R. Meyrelles, D. Just, N. Maulide Deprotective Functionalization: a Direct Conversion of Nms-Amides to Carboxamides Using Carboxylic Acids Angew. Chem. Int. Ed. , e202318304, (2024), DOI: 10.1002/anie.202318304 15. J. Hipólito, R. Meyrelles, B. Maryasin, L. G. Alves, A. M. Martins Reactions of Heteroallenes with Salan-based Ti(IV) Complexes: A Joint Experimental and Computational Study Chem. Asian J. , e202400165, (2024), DOI: 10.1002/asia.202400165 14. G. Archer, R. Meyrelles, I. Eder, N. Kovács, B. Maryasin, M. Médebielle, J. Merad Photoredox-Catalyzed α-C-H Monoalkylation of Symmetric Polyols in the Presence of CO2 Angew. Chem. Int. Ed. , e202315329, (2023), DOI: 10.1002/anie.202315329 G. Archer, R. Meyrelles, I. Eder, N. Kovács, B. Maryasin, M. Médebielle, J. Merad Mechanistic Study on Selenium- and Sulfur-mediated Isomerisation of Hydroxamic Acids Chem. Eur. J. , e202302386, (2023), DOI: 10.1002/chem.202302386 12. 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 11. 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 10. 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 9. 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 8. 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 7. 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 5. 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 3. 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 2. 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 |