| Insights into a surprising reaction: The microwave-assisted direct esterification of phosphinic acids G Keglevich, NZ Kiss, Z Mucsi, T Körtvélyesi Organic & Biomolecular Chemistry 10 (10), 2011-2018, 2012 | 121 | 2012 |
| Novel duplication in the F12 gene in a patient with recurrent angioedema N Kiss, E Barabás, K Várnai, A Halász, LÁ Varga, Z Prohászka, H Farkas, ... Clinical Immunology 149 (1), 142-145, 2013 | 98 | 2013 |
| The role of complement in Streptococcus pneumoniae-associated haemolytic uraemic syndrome Á Szilágyi, N Kiss, C Bereczki, G Tálosi, K Rácz, S Túri, Z Györke, ... Nephrology Dialysis Transplantation 28 (9), 2237-2245, 2013 | 88 | 2013 |
| Microwave-assisted esterification of phosphinic acids G Keglevich, E Balint, N Zs Kiss, E Jablonkai, L Hegedus, A Grun, ... Current Organic Chemistry 15 (11), 1802-1810, 2011 | 75 | 2011 |
| An overview of the applications of ionic liquids as catalysts and additives in organic chemical reactions Z Radai, NZ Kiss, G Keglevich Current Organic Chemistry 22 (6), 533-556, 2018 | 72 | 2018 |
| Novel synthesis of phosphinates by the microwave-assisted esterification of phosphinic acids NZ Kiss, K Ludányi, L Drahos, G Keglevich Synthetic Communications® 39 (13), 2392-2404, 2009 | 72 | 2009 |
| Microwave-assisted direct esterification of cyclic phosphinic acids in the presence of ionic liquids NZ Kiss, G Keglevich Tetrahedron Letters 57 (9), 971-974, 2016 | 60 | 2016 |
| Microwave‐Assisted Direct Esterification of Cyclic Phosphinic Acids NZ Kiss, E Boettger, L Drahos, G Keglevich Heteroatom Chemistry 24 (4), 283-288, 2013 | 54 | 2013 |
| A neighbouring group effect leading to enhanced nucleophilic substitution of amines at the hindered α-carbon atom of an α-hydroxyphosphonate NZ Kiss, A Kaszás, L Drahos, Z Mucsi, G Keglevich Tetrahedron letters 53 (2), 207-209, 2012 | 45 | 2012 |
| The Palladium Acetate‐Catalyzed Microwave‐Assisted Hirao Reaction without an Added Phosphorus Ligand as a “Green” Protocol: A Quantum Chemical Study on the Mechanism G Keglevich, R Henyecz, Z Mucsi, NZ Kiss Advanced Synthesis & Catalysis 359 (24), 4322-4331, 2017 | 43 | 2017 |
| A quantum chemical study on the mechanism and energetics of the direct esterification, thioesterification and amidation of 1-hydroxy-3-methyl-3-phospholene 1-oxide Z Mucsi, NZ Kiss, G Keglevich RSC Advances 4 (23), 11948-11954, 2014 | 39 | 2014 |
| Microwave‐Assisted Functionalization of Phosphinic Acids: Amidations versus Esterifications G Keglevich, NZ Kiss, T Körtvélyesi Heteroatom Chemistry 24 (2), 91-99, 2013 | 39 | 2013 |
| Advantages of the microwave tool in organophosphorus syntheses G Keglevich, NZ Kiss, A Grün, E Bálint, T Kovács Synthesis 49 (14), 3069-3083, 2017 | 38 | 2017 |
| Microwave-assisted organophosphorus synthesis G Keglevich, A Grun, E Balint, N Zsuzsa Kiss, E Jablonkai Current Organic Chemistry 17 (5), 545-554, 2013 | 38 | 2013 |
| Direct esterification of phosphinic acids under microwave conditions: extension to the synthesis of thiophosphinates and new mechanistic insights G Keglevich, NZ Kiss, L Drahos, T Körtvélyesi Tetrahedron Letters 54 (6), 466-469, 2013 | 34 | 2013 |
| Palladium-catalyzed C–P cross-coupling between (het) aryl halides and secondary phosphine oxides GG Zakirova, DY Mladentsev, NE Borisova Synthesis 51 (11), 2379-2386, 2019 | 30 | 2019 |
| To date the greenest method for the preparation of α-hydroxyphosphonates from substituted benzaldehydes and dialkyl phosphites G Keglevich, Z Rádai, NZ Kiss Green Processing and Synthesis 6 (2), 197-201, 2017 | 30 | 2017 |
| The synthesis of phosphinates: traditional versus green chemical approaches G Keglevich, NZ Kiss, Z Mucsi, E Jablonkai, E Bálint Green Processing and Synthesis 3 (2), 103-110, 2014 | 29 | 2014 |
| A three-step conversion of phenyl-1H-phosphinic acid to dialkyl phenylphosphonates including two microwave-assisted direct esterification steps N Zsuzsa Kiss, Z Mucsi, E Bottger, L Drahos, G Keglevich Current Organic Synthesis 11 (5), 767-772, 2014 | 28 | 2014 |
| Synthesis and anticancer cytotoxicity with structural context of an α-hydroxyphosphonate based compound library derived from substituted benzaldehydes Z Rádai, T Windt, V Nagy, A Füredi, NZ Kiss, I Ranđelović, J Tóvári, ... New Journal of Chemistry 43 (35), 14028-14035, 2019 | 26 | 2019 |
