Po habilitacji:

1. M. Zahn, G. König , H. Viet Cuong Pham, B. Seroka, R. Lazny, G. Yang, O. Ouerfelli, Z. Lotowski, and T. Rohwerder, Mechanistic details of the actinobacterial lyase-catalyzed degradation reaction of 2-hydroxyisobutyryl-CoA, J. Biol. Chem. 298(1) (2022), 101522; IF 5.157; MNiSzW – 100;  DOI: 10.1016/j.jbc.2021.101522
2. E. Grabowska, M. Czerniecka, U. Czyżewska, A. Zambrzycka, Z. Łotowski, A. Tylicki, Differences in the efficiency of 3-deazathiamine and oxythiamine pyrophosphates as inhibitors of pyruvate dehydrogenase complex and growth of HeLa cells in vitro, Journal of Enzyme Inhibition and Medicinal Chemistry 36(1) (2021) 122-129 IF 4.310 MNiSzW – 140 DOI: 10.1080/14756366.2020.1844681
3. B. Seroka, Z. Łotowski, A. Hryniewicka, L. Rárová, R.R. Sicinski, A.M. Tomkiel, J. W. Morzycki, Synthesis of new cisplatin derivatives from bile acids, Molecules  25 (2020)655 (Open Access) doi:10.3390/molecules25030655IF 3.060 MNiSzW – 100
4. B. Seroka, Z. Łotowski, A. Wojtkielewicz,  P. Bazydło, E. Dudź, A. Hryniewicka, J.W. Morzycki, Synthesis of steroidal 1,2- and 1,3-diamines as ligands for transition metal ion complexation, Steroids 147, 19-27 (2019) IF 2.523 MNiSzW - 70
5. A. Tylicki, Z. Łotowski, M. Siemieniuk, A. Ratkiewicz, Thiamine and selected thiamine antivitamins - biological activity and methods of synthesis, Bioscience Rep. 38(1) (2018) 1-23.  IF(2017) 2.906; MNiSzW - 20
6. A. Hryniewicka, Z. Łotowski, B. Seroka, S. Witkowski, J. W. Morzycki, Synthesis of a cisplatin derivative from lithocholic acid, Tetrahedron, 2018, 74(38), 5392-5398 + supplementary materials 1-32. IF(2017) 2.651, MNiSW-30, DOI: 10.1016/j.tet.2018.01.007
7. A.M Tomkiel, U. Kiełczewska, B. Seroka, Z. Łotowski, Dimeric Cholaphanes with Disulfide Spacers, J. Sulfur Chem. (2018) 39(3) 252-256, doi: 10.1080/17415993.2017.1414820, IF(2016) 1.271; MNiSzW -20.
8. A. Wojtkielewicz, Z. Łotowski, J. W. Morzycki, One-stepsynthesis of nitriles from acids, esters and amides using DIBAL-H and ammonium chloride, Synlett 26 (2015) 2288-2292, IF 2.419
9. A. M. Tomkiel, J. Kowalski, J. Płoszyńska, L. Siergiejczyk, Z. Łotowski, A. Sobkowiak, J. W. Morzycki , Electrochemical synthesis of glycocnjugates from activated sterol derivatives, Steroids, 2014, 82,60-67IF 2,803;MNiSzW -27
10. Tomkiel A.M., Brzeziński K., Łotowski Z., Siergiejczyk L., Wałejko P., Witkowski S., Kowalski J., Płoszyńska J., Sobkowiak A., Morzycki J.W., Electrochemical synthesis of glycoconjugates of 3β-hydroxy-∆5 steroids by using non-activated sugars and steroidal thioethers, Tetrahedron, 2013, 69, 8904-8913,    IF 2,899;  MNiSzW -30         

Po doktoracie:

1. Morzycki J.W., Wilczewska A.Z., Łotowski Z. “On reaction of enamides with acetyl nitrate”, Tetrahedron Lett., 1996, 37, 2079-2082. IF = 2.497
2. Morzycki J.W., Łotowski Z., Wilczewska A.Z., Stuart J.D. “Synthesis of 4,17-diazasteroid inhibitors of  human 5a-reductase”, Bioorg. Med. Chem., 1996, 4, 1209-1215. IF = 1.716 (1997)
3. Plesnar Z., Malanowski S., Łotowski Z., Morzycki J.W., Frelek J., Wójcik J. “Stereospecific association of C-20 epimers of 3b-hydroxy-16-oxo-24-nor-17-azachol-5-eno-23-nitrile”, Z. Naturforsch., 1997, 52b, 749-756. IF = 0.864
4. Morzycki J.W., Kalinowski S., Łotowski Z., Rabiczko J. “Synthesis of dimeric steroids as components of lipid membranes”, Tetrahedron, 1997, 53, 10579-10590. IF = 2.327
5. Morzycki J.W., Łotowski Z., Stępniowska M., Gryszkiewicz A., Wilczewska A.Z.  “Nitration of N‑acetyl enamines with acetyl nitrate”, Tetrahedron,1997, 53, 16161-16168. IF = 2.327
6. Dubis A.T., Łotowski Z., Siergiejczyk L., Wilczewska A.Z., J. W. Morzycki J.W. “Study of hydrogen bonding in nitro enamides”, J. Chem. Res., 1998, 170-171 (S); 0813-0821 (M). IF = 0.687
7. Łotowski Z., Morzycki J.W., Siciński R.R. “Preparation of 7a- and 7b-methyl-cholestane derivatives by kinetic separation of the diastereomeric mixture”, Tetrahedron Asymmetry, 1998, 9, 1627-1633. IF = 2.484
8. Morzycki J.W., Gryszkiewicz A., Lotowski Z., Szczepek W.J. “Reduction of 2-nitro-5a-cholestan-3‑one, its enol tautomer and 2-nitro-5a-cholest-2-en-3-amine derivatives. Synthesis of bis-steroidal pyrazines”, Collect. Czech. Chem. Commun.1998, 63, 1589-1596. IF = 0.546
9. Łotowski Z., Gryszkiewicz A., Borowiecka J.B., Nikitiuk A., Morzycki J.W. ”A facile synthesis of symmetrical dimeric steroid-pyrazines”, J. Chem. Res. (S), 1999, 662-663. IF = 0.560
10. Łotowski Z., Dubis E.N., Morzycki J.W. “Functionalization of dimeric cholestanopyrazines at the quasi-benzylic position”, Monatsh. Chem., 2000, 131, 65-71. IF = 0.783   
11. Kalinowski S., Łotowski Z., Morzycki J.W. “The influence of bolaamphiphilic steroid dimer on the formation and structure of bilayer lipid membranes”, Cell. Mol. Biol. Lett., 2000, 5, 107-128. IF = 0.960
12. Łotowski Z., Maj J., Morzycki J.W. “3-Bromomethylcholest-2-ene and its reactions”, Chem. Pap., 2001, 55, 118-120. IF = 0.349
13. Łotowski Z., Morzycki J.W., Niewczas I.S., Zdanowicz M. “Synthesis of cis and trans isomers of D-ring linked bis-steroid pyrazines from 16a-bromo-17-oxosteroids”, Collect. Czech. Chem. Commun., 2002, 67, 47-54. IF = 0.848
14. Żebrowska A., Krysiński P., Łotowski Z. “Electrochemical studies of blocking properties of solid supported tethered lipid membranes on gold”, Bioelectrochem., 2002, 56, 179-184. IF = 1.960
15. Krysiński P., Żebrowska A., Pałys B., Łotowski Z. “Spectroscopic and electrochemical studies of bilayer lipid membranes tethered to the surface of gold”, J. Electrochem. Soc., 2002, 149, E189-E194. IF = 2.330
16. Łotowski Z., „Kwasy żółciowe jako komponenty architektoniczne w chemii supramolekularnej”, Wiad. Chem., 2003, 57, 1093-1132.
17. Łotowski Z., “Zbiór zadań testowych z chemii organicznej dla kierunków przyrodniczych niechemicznych”, Wyd. Uniwersytetu w Białymstoku, Białystok, 2003.
18. Łotowski Z., Guzmański D. “New cyclic dimers of cholic acid”, Monatsh. Chem., 2005, 136, 153-158. IF = 0.935
19. Łotowski Z., D. Guzmański D. “New acyclic dimers of cholic acid with oxamide and hydrazide spacers”, Monatsh. Chem., 2006, 137, 117-124. IF = 0.920
20. Łotowski Z., Piechowska J., Jarocki Ł. “Dimeric cholaphanes with oxamide spacers”, Monatsh. Chem., 2008, 139, 213-222. IF = 1.426
21. Kowalski J., Łotowski Z., Morzycki J.W., Płoszyńska J., Sobkowiak A., Wilczewska A.Z. “Unusual electrochemical oxidation of   cholesterol”, Steroids,2008, 73, 543-548. IF = 2.588
22. Łotowski Z., Kulesza U. ”Studies on the synthesis of cholane derivatives containing a mercapto group and their dimers with disulfide spacers. Part 1. 24-Mercapto-5β-cholane-3α,7α,12α-triol and its C(24)–C(24’) disulfide dimer”, J. Sulfur Chem., 2010, 31(2), 97-102. IF = 0.750
23. Morzycki J.W., Łotowski Z., Siergiejczyk L., Wałejko P., Witkowski S., Kowalski J., Płoszyńska J., Sobkowiak A. “A selective electrochemical method of glycosylation of 3b-hydroxy-D⁵-steroids”, Carbohyd. Res., 2010, 345 (8), 1051 – 1055. IF = 1.898
24. Łotowski Z., Kulesza U., Tomkiel A.M. “Studies on the synthesis of cholane derivatives containing a mercapto group and their dimers with disulfide spacers. Part 2. 3α-Mercapto-5β-cholane-7α,12α,24-triol and its C(3)–C(3’) disulfide dimer”, J. Sulfur Chem., 2010, 31 (6), 525-532. IF = 0.750
25. Brzezinski K., Tomkiel A.M., Łotowski Z., Morzycki J., Dauter Z. ”Bis[3α,7α,12α-tris(4-nitrobenzoyloxy)-5β-cholan-24-yl] disulfide-ethyl acetate-n-hexane (4/4/1)”, Acta Crystallogr. E, 2011, E67, o74-o75 +supplementary materials, sup1-sup45. IF = 0.413 (2010)
26. Morzycki J.W., Łotowski Z. “N-Alkylation of 17-azasteroids”, Steroids, 1994, 59, 30-33. IF 1.065, 
27. Morzycki J.W., Łotowski Z. “Studies on the Construction of the 2-Isooctyl Side Chain   in 17-Azasteroids”, Monatsh. Chem.1995, 126, 119-128. IF 0.643,  
28. Morzycki J.W., Łotowski Z., Siergiejczyk L., Lipkowski J., Tabaszewska A., Wójcik J. „Structure of 3b-hydroxy-16-oxo-24-nor-17-azachol-5-eno-23-nitrile and its 20S epimer”, Steroids, 1995, 60, 195-203. IF 1.396,                
29. Morzycki J.W., Łotowski Z. „Synthesis of 17-azacholesterol”, Heterocycles, 1995, 41, 931-936. IF 0.916,               
30. Morzycki.W., Wilczewska A.Z., Żochowska E., Łotowski Z. “Stereoselective reduction of the double bond in delta5-3-oxo-4-azasteroids”, Heterocycles, 1995, 41, 2729-2736. IF 0.916