| Strategic Application of Residence-Time Control in Continuous-Flow Reactors IM Mándity, SB Ötvös, F Fülöp ChemistryOpen 4 (3), 212-223, 2015 | 100 | 2015 |
| Continuous Flow Asymmetric Synthesis of Chiral Active Pharmaceutical Ingredients and their Advanced Intermediates SB Ötvös, CO Kappe Green Chemistry 23 (17), 6117-6138, 2021 | 91 | 2021 |
| Highly Efficient 1, 4‐Addition of Aldehydes to Nitroolefins: Organocatalysis in Continuous Flow by Solid‐Supported Peptidic Catalysts SB Ötvös, IM Mándity, F Fülöp ChemSusChem 5 (2), 266-269, 2012 | 87 | 2012 |
| Continuous‐flow solid‐phase peptide synthesis: a revolutionary reduction of the amino acid excess IM Mándity, B Olasz, SB Ötvös, F Fülöp ChemSusChem 7 (11), 3172-3176, 2014 | 67 | 2014 |
| Multigram-Scale Flow Synthesis of the Chiral Key Intermediate of (–)-Paroxetine Enabled by Solvent-Free Heterogeneous Organocatalysis SB Ötvös, MA Pericas, CO Kappe Chemical Science 10 (48), 11141-11146, 2019 | 65 | 2019 |
| Alkyne-azide cycloadditions with copper powder in a high-pressure continuous-flow reactor: high-temperature conditions versus the role of additives. SB Ötvös, IM Mándity, L Kiss, F Fülöp Chemistry, an Asian journal 8 (4), 800-808, 2013 | 55 | 2013 |
| Asymmetric aldol reaction in a continuous-flow reactor catalyzed by a highly reusable heterogeneous peptide SB Ötvös, IM Mándity, F Fülöp Journal of catalysis 295, 179-185, 2012 | 54 | 2012 |
| Telescoped Continuous Flow Synthesis of Optically Active γ-Nitrobutyric Acids as Key Intermediates of Baclofen, Phenibut, and Fluorophenibut SB Ötvös, P Llanes, MA Pericas, CO Kappe Organic Letters 22 (20), 8122-8126, 2020 | 52 | 2020 |
| Harnessing the Versatility of Continuous-Flow Processes: Selective and Efficient Reactions IM Mándity, SB Ötvös, G Szőlősi, F Fülöp The Chemical Record 16 (3), 1018-1033, 2016 | 48 | 2016 |
| Stereoselective syntheses and transformations of chiral 1, 3-aminoalcohols and 1, 3-diols derived from nopinone Z Szakonyi, T Gonda, SB Oetvoes, F Fueloep Tetrahedron: Asymmetry 25 (15), 1138-1145, 2014 | 43 | 2014 |
| Highly Selective Continuous-Flow Synthesis of Potentially Bioactive Deuterated Chalcone Derivatives CT Hsieh, SB Ötvös, YC Wu, IM Mándity, FR Chang, F Fülöp ChemPlusChem 80 (5), 859-864, 2015 | 40 | 2015 |
| A High-Yielding Synthesis of EIDD-2801 from Uridine A Steiner, D Znidar, SB Ötvös, DR Snead, D Dallinger, CO Kappe European Journal of Organic Chemistry 2020 (43), 6736-6739, 2020 | 36 | 2020 |
| Flow chemistry as a versatile tool for the synthesis of triazoles SB Ötvös, F Fülöp Catalysis Science & Technology 5 (11), 4926-4941, 2015 | 36 | 2015 |
| Heterogeneous Dipeptide-Catalyzed α-Amination of Aldehydes in a Continuous-Flow Reactor: Effect of Residence Time on Enantioselectivity SB Ötvös, A Szloszár, IM Mándity, F Fülöp Advanced Synthesis & Catalysis 357 (16-17), 3671-3680, 2015 | 35 | 2015 |
| Continuous-flow oxidative homocouplings without auxiliary substances: Exploiting a solid base catalyst SB Ötvös, Á Georgiádes, R Mészáros, K Kis, I Pálinkó, F Fülöp Journal of Catalysis 348, 90-99, 2017 | 34 | 2017 |
| Efficient continuous-flow synthesis of novel 1, 2, 3-triazole-substituted β-aminocyclohexanecarboxylic acid derivatives with gram-scale production SB Ötvös, Á Georgiádes, IM Mándity, L Kiss, F Fülöp Beilstein Journal of Organic Chemistry 9 (1), 1508-1516, 2013 | 33 | 2013 |
| Highly selective deuteration of pharmaceutically relevant nitrogen-containing heterocycles: A flow chemistry approach SB Ötvös, IM Mándity, F Fülöp Molecular diversity 15, 605-611, 2011 | 33 | 2011 |
| Continuous-Flow Synthesis of Deuterium-Labeled Antidiabetic Chalcones: Studies towards the Selective Deuteration of the Alkynone Core SB Ötvös, CT Hsieh, YC Wu, JH Li, FR Chang, F Fülöp Molecules 21 (3), 318; doi:10.3390/molecules21030318, 2016 | 31 | 2016 |
| Exploring New Parameter Spaces for the Oxidative Homocoupling of Aniline Derivatives: Sustainable Synthesis of Azobenzenes in a Flow System Á Georgiádes, SB Ötvös, F Fülöp ACS Sustainable Chemistry & Engineering 3 (12), 3388-3397, 2015 | 29 | 2015 |
| A layered double hydroxide, a synthetically useful heterogeneous catalyst for azide-alkyne cycloadditions in a continuous-flow reactor SB Ötvös, Á Georgiádes, M Ádok-Sipiczki, R Mészáros, I Pálinkó, P Sipos, ... Applied Catalysis A: General 501, 63-73, 2015 | 29 | 2015 |
Istvan ManditySemmelweis University Institute of Organic Chemistry/ Research Centre for Natural SciencesZweryfikowany adres z pharma.semmelweis-univ.hu
