| Bridging homogeneous and heterogeneous catalysis by heterogeneous single-metal-site catalysts X Cui, W Li, P Ryabchuk, K Junge, M Beller Nature Catalysis 1 (6), 385-397, 2018 | 812 | 2018 |
| Intermetallic nickel silicide nanocatalyst—A non-noble metal–based general hydrogenation catalyst P Ryabchuk, G Agostini, MM Pohl, H Lund, A Agapova, H Junge, K Junge, ... Science advances 4 (6), eaat0761, 2018 | 120 | 2018 |
| Molecularly defined manganese catalyst for low-temperature hydrogenation of carbon monoxide to methanol P Ryabchuk, K Stier, K Junge, MP Checinski, M Beller Journal of the American Chemical Society 141 (42), 16923-16929, 2019 | 71 | 2019 |
| Heterogeneous Nickel-Catalysed Reversible, Acceptorless Dehydrogenation of N-Heterocycles for Hydrogen Storage P Ryabchuk, A Agapova, CR Kreyenschulte, H Lund, H Junge, K Junge, ... Chemical Communications 55, 4969-4972, 2019 | 52 | 2019 |
| Formal substitution of bromocyclopropanes with nitrogen nucleophiles JE Banning, J Gentillon, PG Ryabchuk, AR Prosser, A Rogers, A Edwards, ... The Journal of Organic Chemistry 78 (15), 7601-7616, 2013 | 41 | 2013 |
| Toward catalytic, enantioselective chlorolactonization of 1, 2-disubstituted styrenyl carboxylic acids SE Denmark, P Ryabchuk, MT Burk, BB Gilbert The Journal of Organic Chemistry 81 (21), 10411-10423, 2016 | 35 | 2016 |
| Formal nucleophilic substitution of bromocyclopropanes with azoles P Ryabchuk, M Rubina, J Xu, M Rubin Organic letters 14 (7), 1752-1755, 2012 | 35 | 2012 |
| Organoselenium-catalyzed enantioselective syn-dichlorination of unbiased alkenes BB Gilbert, STC Eey, P Ryabchuk, O Garry, SE Denmark Tetrahedron 75 (31), 4086-4098, 2019 | 34 | 2019 |
| Cascade synthesis of pyrroles from nitroarenes with benign reductants using a heterogeneous cobalt catalyst P Ryabchuk, T Leischner, C Kreyenschulte, A Spannenberg, K Junge, ... Angewandte Chemie 132 (42), 18838-18844, 2020 | 28 | 2020 |
| Dual control of the selectivity in the formal nucleophilic substitution of bromocyclopropanes en route to densely functionalized, chirally rich cyclopropyl derivatives P Ryabchuk, A Edwards, N Gerasimchuk, M Rubina, M Rubin Organic letters 15 (23), 6010-6013, 2013 | 26 | 2013 |
| Rearrangements of cyclopropenes into five-membered aromatic heterocycles: mechanistic aspect M Rubin, PG Ryabchuk Chemistry of Heterocyclic Compounds 48, 126-138, 2012 | 20 | 2012 |
| Development of bulk organic chemical processes—history, status, and opportunities for academic research C Schneider, T Leischner, P Ryabchuk, R Jackstell, K Junge, M Beller CCS Chemistry 3 (3), 512-530, 2021 | 16 | 2021 |
| Templated Assembly of Chiral Medium-Sized Cyclic Ethers via 8-endo-trig Nucleophilic Cyclization of Cyclopropenes P Ryabchuk, JP Matheny, M Rubina, M Rubin Organic letters 18 (24), 6272-6275, 2016 | 16 | 2016 |
| Methyl formate as a hydrogen energy carrier R Sang, Z Wei, Y Hu, E Alberico, D Wei, X Tian, P Ryabchuk, ... Nature Catalysis 6 (6), 543-550, 2023 | 11 | 2023 |
| From mobile phones to catalysts: E-waste-derived heterogeneous copper catalysts for hydrogenation reactions P Ryabchuk, M Anwar, S Dastgir, K Junge, M Beller ACS Sustainable Chemistry & Engineering 9 (30), 10062-10072, 2021 | 11 | 2021 |
| Silicon-Enriched Nickel Nanoparticles for Hydrogenation of N-Heterocycles in Aqueous Media S Mao, P Ryabchuk, S Dastgir, M Anwar, K Junge, M Beller ACS Applied Nano Materials 5 (4), 5625-5630, 2022 | 10 | 2022 |
| A convenient and stable heterogeneous nickel catalyst for hydrodehalogenation of aryl halides using molecular hydrogen DK Leonard, P Ryabchuk, M Anwar, S Dastgir, K Junge, M Beller ChemSusChem 15 (5), e202102315, 2022 | 9 | 2022 |
| Heterogeneous iron-catalyzed hydrogenation of nitroarenes under water-gas shift reaction conditions P Ryabchuk, K Junge, M Beller Synthesis 50 (22), 4369-4376, 2018 | 7 | 2018 |
| Preparative resolution of bromocyclopropylcarboxylic acids A Edwards, P Ryabchuk, A Barkov, M Rubina, M Rubin Tetrahedron: Asymmetry 25 (23), 1537-1549, 2014 | 6 | 2014 |
| Preparation of a diisopropylselenophosphoramide catalyst and its use in enantioselective sulfenoetherification SE Denmark, P Ryabchuk, HM Chi, A Matviitsuk Organic syntheses; an annual publication of satisfactory methods for the …, 2019 | 5 | 2019 |
