| An update on “selenium containing compounds from poison to drug candidates: A review on the GPx-like activity” AJ Pacuła, F Mangiavacchi, L Sancineto, JL Eder, J Ścianowski, C Santi Current chemical biology 9 (2), 97-112, 2016 | 89 | 2016 |
| New glutathione peroxidase mimetics—Insights into antioxidant and cytotoxic activity AJ Pacuła, KB Kaczor, A Wojtowicz, J Antosiewicz, A Janecka, A Długosz, ... Bioorganic & Medicinal Chemistry 25 (1), 126-131, 2017 | 63 | 2017 |
| Convenient route to dialkyl diselenides from alkyl tosylates. Synthesis of di (cis-myrtanyl) diselenide J Ścianowski Tetrahedron letters 46 (19), 3331-3334, 2005 | 57 | 2005 |
| Highly efficient synthesis and antioxidant capacity of N-substituted benzisoselenazol-3 (2 H)-ones AJ Pacuła, J Ścianowski, KB Aleksandrzak RSC Advances 4 (90), 48959-48962, 2014 | 55 | 2014 |
| Selenium‐Catalyzed Oxacyclization of Alkenoic Acids and Alkenols L Sancineto, F Mangiavacchi, C Tidei, L Bagnoli, F Marini, A Gioiello, ... Asian Journal of Organic Chemistry 6 (8), 988-992, 2017 | 54 | 2017 |
| New chiral ebselen analogues with antioxidant and cytotoxic potential AJ Pacuła, KB Kaczor, J Antosiewicz, A Janecka, A Długosz, T Janecki, ... Molecules 22 (3), 492, 2017 | 53 | 2017 |
| Syntheses and reactions of new optically active terpene dialkyl diselenides J Ścianowski, Z Rafiński, A Wojtczak European journal of organic chemistry 2006 (14), 3216-3225, 2006 | 50 | 2006 |
| Synthesis and reactions of enantiomerically pure dialkyl diselenides from the p-menthane group Z Rafiński, J Ścianowski Tetrahedron: Asymmetry 19 (10), 1237-1244, 2008 | 47 | 2008 |
| Syntheses and reactions of terpene β-hydroxyselenides and β-hydroxydiselenides J Ścianowski, Z Rafiński, A Wojtczak, K Burczyński Tetrahedron: Asymmetry 20 (24), 2871-2879, 2009 | 39 | 2009 |
| New chiral selenium electrophiles derived from functionalized terpenes J Ścianowski, Z Rafiński, A Szuniewicz, A Wojtczak Tetrahedron 65 (49), 10162-10174, 2009 | 39 | 2009 |
| Asymmetric selenocyclization with the use of dialkyl monoterpene diselenides Z Rafiński, J Ścianowski, A Wojtczak Tetrahedron: Asymmetry 19 (2), 223-230, 2008 | 32 | 2008 |
| The Use of Sulfides Derived from Carane, P-Menthane, Pinane, and Bornane in the Synthesis of Optically Active Epoxides A Banach, J Ścianowski, P Ozimek Phosphorus, Sulfur, and Silicon and the Related Elements 189 (2), 274-284, 2014 | 29 | 2014 |
| Synthesis and reactions of the optically active selenols derived from monoterpenes J Ścianowski, J Rafalski, A Banach, J Czaplewska, A Komoszyńska Tetrahedron: Asymmetry 24 (18), 1089-1096, 2013 | 27 | 2013 |
| Bioselectivity induced by chirality of new terpenyl organoselenium compounds M Obieziurska, AJ Pacuła, A Długosz-Pokorska, M Krzemiński, A Janecka, ... Materials 12 (21), 3579, 2019 | 26 | 2019 |
| Synthesis and reactions of the optically active dialkyl diselenides from the pinane group Z Rafinski, J Scianowski, A Wojtczak Letters in Organic Chemistry 6 (4), 321-328, 2009 | 25 | 2009 |
| Organoselenium compounds as antioxidants. M Obieziurska-Fabisiak, AJ Pacuła-Miszewska, A Laskowska, ... ARKIVOC: Online Journal of Organic Chemistry 2023, 2023 | 22 | 2023 |
| Asymmetric synthesis of cyclopropyl phosphonates using chiral terpenyl sulfonium and selenonium ylides WH Midura, J Ścianowski, A Banach, A Zając Tetrahedron: Asymmetry 25 (22), 1488-1493, 2014 | 21 | 2014 |
| Application of Organolithium and Related Reagents in Synthesis. Part 111. Metallation of 2-Methyl- and 4-Methylnicotinic Acids. A Useful Method for Preparation of … J Epsztajn, MW Płotka, J Ścianowski Synthetic communications 22 (9), 1239-1247, 1992 | 21 | 1992 |
| Terpenyl selenides: Synthesis and application in asymmetric epoxidation A Banach, J Ścianowski, M Uzarewicz‐Baig, A Wojtczak European Journal of Organic Chemistry 2015 (16), 3477-3485, 2015 | 20 | 2015 |
| In vitro anti-prostate cancer activity of two ebselen analogues KB Kaczor-Keller, A Pawlik, J Scianowski, A Pacuła, M Obieziurska, ... Pharmaceuticals 13 (3), 47, 2020 | 19 | 2020 |
Agata PacułaVerified email at umk.pl
