Mgr. Kotrusz Peter, PhD.

Mustonen, K., Hofer, Ch., Kotrusz, P., , Markevich, A., Hulman, M., Mangler, C., Susi, T., Pennycook, T.J., Hricovini, K., Richter, Ch. M., Meyer, J.C., Kotakoski, J., and Skákalová, V.: Towards exotic layered materials: 2D cuprous iodide, Adv. Mater. 34 (2022) 2106922.

1. Marrazzo, A.: NPJ 2D Mater. Appl. 6 (2022) 30.
2. Yu, J.H.: Surfaces Interfac. 30 (2022) 101885.
3. Xu, J.: Nanoscale 14 (2022) 17401.
4. Ma, M.-Y.: Materials 15 (2022) 7715.
5. Mohebpour, M.A.: Phys. Rev. B 106 (2022) 125405.
6. Yu, J.: Vacuum 207 (2023) 111693.
7. Shakourian, M.: J. Comput. Electron. 22 (2023) 96.
8. Ma, H.: Small 19 (2023) Iss. 1.
9. Ma, M.Y.: Mater. Today Nano 22 (2023) 100304.
10. Peng, B.Q.: Adv. Electron. Mater. 9 (2023) Iss. 5.
11. Zhang, X.M.: Mater. Today Energy 34 (2023) 101293.

Cossutta, M., Vretenar, V., Centeno, T.A., Kotrusz, P., McKechnie, J., and Pickeringe, S.J.: A comparative life cycle assessment of graphene and activated carbon in a supercapacitor application, J.  Cleaner Prod. 242 (2020) 118468. (Not IEE SAS)

1. Wu, J.Z.: Energy Fuels 34 (2020) 16220.
2. Yadav, KK.: J. Cleaner Prod. 276 (2020) 124240.
3. Mendoza, R.: Synthet. Metals 268 (2020) 116500.
4. Du, Y.Q.: Coatings 10 (2020) 892.
5. Gul, P.: Separ. Sci Technol. 56 (2021) 2026.
6. Ghai, V.: Carbon Lett. 31 (2021) 473.
7. Aadil, M.: Ceram. Inter. 46 (2020) 17836.
8. Altuntas, D.B.: Energy Sources A 42 (2020) 2346.
9. Zhang, C.Y.: Ionics 26 (2020) 5179.
10. Lei, C.H.: Proc. Inst. Mechan. Engn. A 235 (2021) 914.
11. Selvaraj, T.: Mater. Res. Bull. 126 (2020) 110839.
12. Wang, S.W.: Inorg. Chem. Comm. 114 (2020) 107822.
13. Gonzalez-Poggini, S.: Process. 9 (2021) 2160.
14. Dubey, P.: CHEMISTRYSELECT 6  (2021) 11736.
15. Rajaputra, S.S.: J. Electrochem. Energy Conver. Storage 18 (2021) 041008.
16. Jiang, Z.X.: BIOCHAR 3 (2021) 701.
17. Yu, H.: Canad. J. Chem. Engn. 100 (2022) 2872.
18. Azhar, S.: RSC Adv. 11  (2021) 30510.
19. Chang, B.P.:  Renewable Sustain. Energy Rev. 152 (2021) 111666.
20. Safian, M.T.U.: J. Cleaner Prod. 318 (2021) 128603.
21. Torres, F.G.: Sustain. Mater. Technol. 29 (2021) e00310.
22. Rajaputra, S.S.: Ionics 27 (2021) 4069.
23. Melzack, N.: Front. Energy Res. 9 (2021) 699919.
24. Shaker, M.: New Carbon Mater. 36 (2021) 546.
25. Hu, Y.M.: J. Analyt.  Applied Pyrol. 157 (2021) 105221.
26. Yuan, C.Y.: Chinese Chem. Lett. 32 (2021) 2079.
27. Zhang, H.Y.: Electrochim. Acta 389 (2021) 138684.
28. Hu, S.C.: Renewable Energy 177 (2021) 82.
29. Liu, H.: Bull. Chem. Soc Japan 94 (2021) 1705.
30. Herou, S.: Adv. Sci 8 (2021) 2100016.
31. Ajdari, F.B.: J. Molecul. Liquids 333 (2021) 116007.
32. Arvidsson, R.: J. Cleaner Prod. 300 (2021) 126999.
33. Lu, Z.J.: J. Alloys Comp. 856 (2021) 158075.
34. Wang, Y.Y.: ECS J. Solid State Sci Technol. 10 (2021) 031003.
35. Ma, J.Y.: New J. Chem. 45 (2021) 3418.
36. Beloin-Saint-Pierre, D.: Inter. J. Life Cycle Assess. 26 (2021) 327.
37. Kim, HR.: J. Cleaner Prod. 284 (2021) 125449.
38. Wang, Y.Y.: J. Mater. Sci-Mater. Electron. 32 (2021) 6965.
39. Kumar, S.: J. Alloys Comp. 858 (2021) 157671.
40. Cheng, J.: Energy 215 (2021) 119144.
41. Zhang, C.: Inter. J. Life Cycle Assess. (2022).
42. Islam, M.A.: Applied Phys. Rev. 9 (2022) 041301.
43. Zhang, C.: J. Cleaner Prod. 375 (2022) 134044.
44. Glogic, E.: ACS Sustainable Chem. Engn. 10 (2022) 15025.
45. Hatzfeld, T.: Build. Environ.  224  (2022) 109520.
46. Nargatti, K.: Carbohydrate Polym. 297 (2022) 120039.
47. Zhang, C.: J. Cleaner Prod. 370 (2022) 133244.
48. Gerasimenko, A.Y.: Nanomater. 12 (2022) 2812.
49. Tyagi, A.: J. Electron. Mater. 51 (2022) 5670.
50. Nugroho, A.: Lett. Mater. 12 (2022) 169.
51. Melzack, N.: Sci Rep. 12 (2022) 8911.
52. Zhang, Y.: Fuel Process. Technol. 233 (2022) 107307.
53. Gao, XL.: Applied Surface Sci 595 (2022) 153571.
54. Samage, A.: Chem. Engn. J. 435 (2022) 134952.
55. Heidari, A.: J. Cleaner Prod. 357 (2022) 131968.
56. Pryce, D.: Sci Total Environ. 817 (2022) 152985.
57. Pershaanaa, M.: J. Energy Storage 50 (2022) 104599.
58. Liao, Z.: Carbohydrate Polym. 286 (2022) 119287.
59. Spreafico, C.: Sustainab. Production Consum. 30 (2022) 889.
60. Marken, F.: Applied Surface Sci 609 (2023) 155397.
61. Witoon, T.: Inter. J. Hydrogen Energy 47 (2022) 42185.
62. Maklavany, D.M.: ACS Sustainable Chem. Engn. 11 (2023) 9816.
63. Azizi, S.: Diamond Relat. Mater. 137 (2023) 110061.
64. Babaahmadi, V.: Nanomater. 13 (2023) 1866.
65.  Xu, J.: J. Energy Storage 68 (2023) 107819.
66. Dhanda, A.: Environmen. Res. 231 (2023) 116143.
67. Mousavi-Avval, S.H.: Renewab. Sustainab. Energy Rev. 180 (2023) 113302.
68. Pereira, J.: Applied Sci 13 (2023) 4070.
69. de Lima, L.R.M.: Sci Total Environ. 871 (2023) 162140.
70. Skuse, C.: Desalination 551 (2023) 116418.
71. Niu, D.: Energy Rep. 9 (2023) 2566.
72. Jiao, Y.: J. Energy Storage 57 (2023) 106167.
73. Zhang, C.: Inter. J. Life Cycle Assessm. 28 (2023) 80.

Guardia, L., Suárez, L., Querejeta, N., Vretenár, V., Kotrusz, P., Skákalová, V., and Centeno, T.A.: Biomass waste-carbon/reduced graphene oxide composite electrodes for enhanced supercapacitors, Electrochim. Acta 298 (2019) 910-917. (Not IEE SAS)

1. Wang, M.M.: J. Mater. Sci 54 (2019) 14085.
2. Afir, A.: J. Energy Storage 25 (2019) 100852.
3. Zhang, X.Z.: Inter. J. Electrochem. Sci 14 (2019) 8793.
4. Li, P.X.: J. Alloys Comp. 791 (2019) 152.
5. Li, H.: Adv. Energy Mater. 9 (2019) 1900079.
6. da Silva, L. M.: J. Solid State Electrochem. 23 (2019) 1871.
7. Yang, H.: Front. Chem. 7 (2019) 274.
8. Ren, P.G.: Diamond Relat. Mater. 109 (2020) 108028.
9. Ehsani, A.: Adv. Colloid Interface Sci 284 (2020) 102263.
10. Mir, R.A.: Physica E 124 (2020) 114284.
11. Alcaraz, L.: Front. Chem. 8 (2020) 686.
12. Zhou, Y.L.: Mater. Express 10 (2020) 1364.
13. Gao, Y.: Inter. J. Energy Res. 44 (2020) 10946.
14. He, AJ.: J. Mater. Sci-Mater. Electron. 31 (2020) 13131.
15. Mohamedkhair, A.K.: Arab. J. Chem. 13 (2020) 6161.
16. Wang, D.F.: Inter. J. Energy Res. 44 (2020) 8542.
17. Li, J.B.: Ionics 26 (2020) 3677.
18. Xu, J.: Electrochim. Acta 340 (2020) 135950.
19. Cheng, F.: J. Electrochem. Soc 167 (2020) 040507.
20. Jung, H.Y.: Carbon Lett. 30 (2020) 107.
21. Li, P.X.: Electrochim. Acta 330 (2020) 135334.
22. Fu, H.H.: Inter. J. Hydrogen Energy 45 (2020) 443.
23. Liu, X.: Nano Energy 86 (2021) 106070.
24. Zhao, R.: Small Struct. 2 (2021) 2100132.
25. Lakra, R.: Inorg. Chem. Comm. 133 (2021) 108929.
26. Sundriyal, S.: Resour. Conser. Recyc. 169 (2021) 105548.
27. Zhang, H.H.: Small 17 (2021) 2007311.
28. Wang, Y.: Mater. Today Comm. 26 (2021) 102057.
29. Quan, H.Y.: J. Energy Storage 55 (2022) 105573.
30. Tatrari, G.: J. Energy Storage 53 (2022) 105098.
31. Wang, X.: HELIYON 8  (2022) e10631.
32. Sun, Y.: Carbon 199 (2022) 224.
33. Urena-Torres, V.: Chemengn. 6 (2022) 49.
34. Tung, Y.Y.: J. Micromech. Microengn. 32 (2022) 073001.
35. Dhandapani, E.: J. Energy Storage 52 (2022) 104937.
36. Lu, W.J.: Micromachin. 13 (2022) 905.
37. Gezovic, A.: J. Power Sources 538 (2022) 231561.
38. Kumar, R.: Carbon 193 (2022) 298.
39. Zia, U.: ECS J. Solid State Sci Technol. 11 (2022) 021001.
40. Jiang, G.S.: J. Power Sources 520 (2022) 230886.
41. Xie, Y.Y.: Nano res. 15 (2022) 1399.
42. Ayub, M.: Mater. Sci Engn. B 295 (2023) 116575.
43. Tamang, S.: J. Alloys Comp. 947 (2023) 169588.
44. Idris, M.O.: Chinese J. Chem. Engn. 55 (2023) 277.
45. Ikram, R.: Nanotechnol. Rev. 12 (2023) 20220512.
46. Ayub, M.: Mater. Chem. Phys. 296 (2023) 127202.
47. Rashi.: Ceram. Inter. 49 (2023) 40.

Hulman, M., Sojková, M., Végso, K., Mrkývkova, N., Hagara, J., Hutár, P., Kotrusz, P., Hudec, J., Tokar, K., Majková, E., and Šiffalovič, P.: Polarized Raman reveals alignment of few-layer MoS2 films, J. Phys. Chem. C 123 (2019) 29468-29475.

1. Zuo, S.: Mater. Sci Semicond. Process. 121 (2021) 105457.
2. Rahmati, B.: J. Electron. Mater. 50 (2021) 3645.
3. Bai, X.: J. Hazard. Mater. 416 (2021) 125830.
4. Du, Y.H.: J. Phys.-Cond. Matt. 34 (2022) 224001.
5. Guo, Z.L.: ACS Nano 16 (2022) 11268.
6. Komen, I.: J. Applied Phys. 132 (2022) 173103.
7. Motala, M.J.: Mater. Today Nano 22 (2023) 100319
8. Yu, H.W.: Chem. Mater. 35 (2023) 3484.

Skákalová, V., Kotrusz, P., Jergel, M., Susi, T., Mittelberger, A., Vretenár, V., Šiffalovič, P., Kotakoski, J., Meyer, J.C., and Hulman, M.: Chemical oxidation of graphite: evolution of the structure and properties, J. Phys. Chem. C 122 (2018) 929−935. (Not IEE SAS)

1. Liao, C.: Inter. J. Molecular Sci 19 (2018) 3564.
2. Kamali, A.R.: Applied Surface Sci 476 (2019) 539.
3. Li, Y.: Nanomater. 9 (2019) 590.
4. Yadav, N.: ACS Omega 4 (2019) 9407.
5. Pazarceviren, A.E.: Biomed. Mater.14 (2019) 035018.
6. Lavin-Lopez, M. P.: Colloids Surfaces A 582 (2019) 123935.
7. Chai, W.S.: J. Molecul. Liquids 293 (2019) UNSP 111496.
8. Sun, L.: Chinese J. Chem. Engn. 27 (2019) 2251.
9. Luo, D.: Mater. Today Phys. 9 (2019) UNSP 100097.
#   10. Majumdar D.: Graphene Functionalization Strategies. Carbon Nanostr. Springer 2019. ISBN 978-981-32-9056-3,  pp. 63-103.
11. Xu, Z.-L.: Sci Total Environ. 708 (2020) 134614.
12. Clarke, R.W.: Macromolecul. 53 (2020) 640.
13. Sauermoser, M.: Front. Energy Res. 8 (2020) 13.
14. Dimiev, A.M.: Carbon 166 (2020) 1.
15. Kamali, A.R.: Polymer Degradation Stab.177 (2020) 109184.
16. Bounegru, A.V.: Catalysts 10 (2020) 680.
17. Kamali, A.R.: In Green Production of Carbon Nanomaterials in Molten Salts and Applications. Springer 2020 ISBN: 978-981-15-2373-1.
18. Mintz, K.: Carbon 173 (2021) ‏ 433.
19. Kashif, M.: Arabian J. Chem. 14 (2021) 102953.
20. Mittal, H.: J. Molecul Liquids 323 (2021) 115034.
21. Ostyn, N.R.: Catal. Sci Technol. 11 (2021) 6724.
22. Mackenzie, D.M.A.: 2D Mater. 8 (2021) 045035.
#     23. Fatmawati, D. A.: Rasayan J. Chem. 14 (2021) 2129.
24. Aziz, N.A.A.: IEEE SCOReD 2021, pp. 300.
#     25. Singh, R.: Lecture Notes in Mechanical Engn. (2021) 165.
26. Gasparotto, M.: Inter. J. Molecul. Sci 23 (2022) 1736.
27. Bychko, I.: J. Phys. Chem. Solids 164 (2022) 110614.
28. Zhao, X.: J. Energy Storage 52 (2022) 104642.
29. Zhou, C.L.: Small Methods 7 (2023) Iss. 3.
30. Vieira, M.A.C.: J. Carbon Res. 9 (2023) 60.

Schmiedova, V., Pospisil, J., Kovalenko, A., Ashcheulov, P., Fekete, L., Cubon, T., Kotrusz, P., Zmeskal, O., and Weiter, M.: Physical properties investigation of reduced graphene oxide thin films prepared by material inkjet printing, J. Nanomater. (2017) 3501903. (Not IEE SAS)

1. Antonelou, A.: Carbon 139 (2018) 492.
2. Haque, A.: IEEE Trans. Semicond. Manufact. 31 (2018) 535.
3. Cruz-Aguilar, A.: Mater. Today Comm. 16 (2018) 232.
4. Rabin, N.N.: ACS Omega 3 (2018) 2074.
5. Al-Graiti, W.: ACS Omega 4 (2019) 22169.
6. Belachew, N.: RSC Adv. 9 (2019) 39264.
7. Vieira, D.H.: J. Electron. Mater. 48 (2019) 7991.
8. Madannejad, R.: Chemico-Biol.  Interact. 307 (2019) 206.
9. Fantoni, A.: ENBENG 2019.
10. Fantoni, A.: PIERS-Spring 2019, p. 4180.
11. Liang, Y.J.: Iran. J. Sci Technol.-Trans. Civil Engn. 44 (2020) 1171.
12. Kumar, S.: Solar Energy 208 (2020) 949.
13. Junaid, M.: Molecules 25 (2020) 3646.
14. Chong, W.S.: Mater. Chem. Phys. 249 (2020) 122970.
15. Seera, R.: Crystal Growth Design 20 (2020) 4667.
16. El-Desoky, M.M.: Optic. Quantum Electron. 52 (2020) 315.
17. Goi, E.: PHOTONIX 1 (2020) 3.
18. Karuppannan, S.K.: J. Americ. Chemic. Soc 142 (2020) 3513.
19. Ali, M.D.: Ceram. Inter. 47 (2021) 26224.
20. Yadav, S.: Sustain. Mater. Technol. 29 (2021) e00315.
21. Arjunan, K.K.: ECS J. Solid State Sci Technol. 10 (2021) 045011.
22. Fantoni, A.: Proc. SPIE 11682 (2021) 1168213.
23. Kale, A.J.: Solar Energy 247 (2022) 345.
24. Kumawat, M.K.: J. Mater. Res. 37 (2022) 3394.
25. Baraty, F.: J. Electromagn. Waves Appl. 36 (2022) 2401.
26. Saravanan, K.: J. Electron. Mater. 51 (2022) SI 4169.
27. Rabchinskii, M.K.: Carbon 196 (2022) 264.
28. Shah, D.K.: Mater. Sci Semicond. Process. 147 (2022) 106695.
29. Elanjeitsenni, V.P.: Mater. Res. Express 9 (2022) 022001.
30. Kim, M.: Applied Sci-Basel 12 (2022) 1185.
31. Samriti, M.: Molecul. Systems Design Engn. 7 (2022) 213.
32. Mili, M.: CHEMISTRYSELECT 6  (2022) 9990.
33. Kukhta, A.V.: Applied Nanosci 12 (2022) 665.
34. Al-Amri, A.M.: Coatings 13 (2023) 831.
35. Abdelrazek, M.M.: Optical Quantum Electron. 55 (2023) Iss. 6.

Susi, T., Skákalová, V., Mittelberger, A., Kotrusz, P., Hulman, M., Pennycook, T.J., Mangler, C., Kotakoski, J., and Meyer, J.C.: Computational insights and the observation of SiC nanograin assembly: towards 2D silicon carbide, Sci Reports 7 (2017) 4399. (Not IEE SAS)

1. Gutzler, R.: Zeitschrift Anorgan. Allgem. Chemie 643 (2017) SI1368.
2. Ziatdinov, M.: ACS Nano 11 (2017) 12742.
3. Belarouci, S.: Comput. Mater. Sci 151 (2018) 288.
4. Ulian, G.: Composite Struct. 202 (2018) SI551.
5. Guo, S.-D.: Phys. Chem. Chem. Phys. 20 (2018) 22038.
6. Peng, C.: Materials 11 (2018) 1699.
7. Yaghoubi, A.: Chem. Mater. 30 (2018) 7234.
8. Cai, Z.: Chem. Rev. 118 (2018) 6091.
9. Cao, Y.: Nano Research 11 (2018) 4074.
10. Islam, Md.R.: J. Comput. Electron. 18 (2019) 407.
11. Islam, A.S.M.J.: Mater. Res. Express 6 (2019) 125073.
12. Islam, A.S.M.J.: Nanotechnol. 30 (2019) 445707.
13. Geng, D.: ACS Applied Mater. Interfaces 11 (2019) 39109.
14. Rashid, A.S.: J. Comput. Electron. 18 (2019) 836.
15. Davydov, S.Yu.: Semiconductors 54 (2020) 523.
16. Borlido, P.: Phys. Chem. Chem. Phys. 22 (2020) 8442.
17. Hess, P.: Nanoscale Horizons 5 (2020) 385.
18. Zhou, L.: Nanoscale 12 (2020) 4269.
19. Lee, Y.-T.: Phys. Rev. B 102 (2020) 075143.
20. Islam, A.S.M.J.: Phys. Chem. Chem. Phys. 22 (2020) 13592.
21. Majid, A.: J. Magnetism Magnetic Mater.‏ 503 (2020)  16664.
22. Islam, Md.S.: Sci Rep. 10 (2020) 22050.
23. Ahammed, S.: Nanotechnol. 31 (2020) 505702.
24. Chabi, S.: Nanomater. 10 (2020) 2226.
25. Hassanzada, Q.: Phys. Rev. B 102 (2020) 134103.
26. Manju, M. S.: Applied Surface Sci 541 (2021) 148417.
27. Lingerfelt, D.B.: Nano Lett. 21 (2021) 236.
28. Kilic, M.E.: Carbon 174 (2021) 368.
29. Liu, Q.: Inter. J. Quantum Chem. 121 (2021) 26608.
30. Islam, M.S.: Mater. Today Comm. 26 (2021) 101718.
31. Abdelsalam, H.: Physica E 130 (2021) 114699.
32. Arellano, L.G.: Inter. J. Hydrogen Energy 46 (2021) 20266.
33. Chabi, S.: Nanomater. 11 (2021) 1799.
34. Chowdhury, E.H.: Comput. Mater. Sci 197 (2021) 110580.
35. Nakamura, T.: J. Comput. Chem. 42 (2021) 1817.
36. Kremer, L.F.: J. Applied Phys. 129 (2021) 184302.
37. Mondal, N.S.: Phys. Chem. Chem. Phys. 23 (2021) 11863.
38. Hess, P.: Nanoscale Horizons 6 (2021) 856.
39. Chegel, R.: Solid State Sci 121 (2021) 106737.
40. Karimzadeh, S.: J. Water Process Engn. 44 (2021)102413.
41. Jana, S.: J. Phys.-Cond. Matt. 34 (2022) 053001.
42. Yaqoob, J.: Europ. Phys. J. Plus 137 (2022) 233.
43. Fatima, A.: Inter. J. Quantum Chem. 122 (2022) 26895.
44. Nayir, N.: J. Mater. Res. 37 (2022) 1172.
45. Galashev, A.Y.: Physica E 138 (2022) 115120.
46. Zhang, L.: Front. Chem. 10 (2022) 898174.
47. Majid, A.: Inter. J. Quantum Chem. 122 (2022) 26877.
48. Nguyen, P.M.: ACS Omega 7 (2022) 47642.
49. Zhao, W.-H.: ACS Applied Electr. Mater. 4 (2022) 4903.
50. Herrero, C.P.: J. Phys. Chem. Solids 171 (2022) 110980.
51. Rashid, M.: Mater. Sci Semicond. Process. 151 (2022) 107007.
52. Fatima, K.: J. Chinese Chem. Soc 69 (2022) 1585.
53. Gao, Z.-Y.: Adv. Mater. 34 (2022) 2204779.
54. Zhang, L.: Front. Mater. 9 (2022) 956675.
55. Dindorkar, S.S.: Silicon 14 (2022) 11771.
56. Huang, L.: Vacuum 208 (2023) 111700.
57. Talla, J.A.: J. Comput. Electron. 22 (2023) 68.
58. Liu, Y.: Sci China-Mater. 66 (2023) 35.
59. Nguyen, P.M.: ACS Omega 7 (2023) 47642.
60. Polley, C.M.: Phys. Rev. Lett. 130 (2023) 076203.
61. Tran, H.T.T.: ACS Omega 8 (2023) 25424.

Pospisil, J., Schmiedova, V., Zmeskal, O., Vretenar, V., and Kotrusz, P.: Electrical properties of graphene oxide layers prepared by material inkjet printing, Key Engn. Mater. 674 (2016) 109-114. (Not IEE SAS).

1. Xu, J.: Cailiao Gongcheng-J. Mater. Engn. 46 (2018) 1.

Lobato, B., Vretenár, V., Kotrusz, P., Hulman, M., and Centeno, T.A.: Reduced graphite oxide in supercapacitor electrodes, J. Colloid Interface Sci 446 (2015) 203-207.

1. Prekodravac, J.: Synthetic Metals 209 (2015) 461.
2. Vermisoglou, E.C.: Applied Surface Sci 358 (2015) 110.
3. Zhang, L.: Electrochim. Acta 186 (2015) 522.
4. Vermisoglou, E. C.: Applied Surface Sci 392 (2015) 244.
5. Xu, X.: J. Alloys Compounds 654 (2016) 23.
6. Wan, M.M.: ACS Applied Mater. Interfaces 8 (2016) 1252.
7. Ren, J.: Inter.  J. Electrochem. Sci 11 (2016) 2550.
8. Huang, G.: Electrochimica Acta 196 (2016) 450.
9. Smirnov, M.: J. Power Sources 304 (2016) 102.
#    10. Kumbhar, V.S.: Mater. Sci Semicond. Process. 46 (2016) 29.
11. Yang, H.: J. Phys. Chem. Lett. 8  (2017) 153.
12. Rasul, S.: Carbon 111 (2017) 774.
13. Vermisoglou, E.C.: Applied Surface Sci 392 (2017) 244.
14. Cossutta, M.: Green Chem. 19 (2017) 5874.
15. Kim, H.J.: Chem. Phys. Lett. 686 (2017) 49.
16. El-Gendy, D.M.: Sci Rep. 7 (2017) 43104.
17. Ma, W.: J. Mater. Sci 53 (2018) 12295.
18. Liu, D.: J. Colloid Interface Sci 513 (2018) 295.
19. Vignesh, V.: Colloids Surfaces A 538 (2018) 668.
20. Zhang, X.: Electrochim. Acta 259 (2018) 793.
21. Li, H.: Adv. Energy Mater. 9 (2019) 1900079.
22. Chang, Y.: J. Mater. Sci-Mater. Electron. 30 (2019) 7216.
23. Naik, S.: New J. Chem. 43 (2019) 16017.
#     24. Loganathan, A.: Rasayan J. Chem. 12 (2019) 1710.
25. Ashraf, M.: Chem.-Europ. J. 27 (2021) 6973.
26. Prasad, A.K.: Applied Surface Sci 564 (2021) 150393.
27. Tang, C.C.: J. Colloid Interface Sci 648 (2023) 181.

Meško, M., Vretenár, V., Kotrusz, P., Hulman, M., and Skákalová, V.: Synthesis of carbon nanowalls on macroporous nickel foam by atmospheric glow discharge chemical vapour deposition, Phys. Status Solidi B 251 (2014) 933–936. (Not IEE SAS)

1. Bo, Z.: Phys. Status Solidi B 252 (2015) 2236.

Skákalová, V., Vretenár, V., Kopera, L., Kotrusz, P., Mangler, C., Meško, M., Meyer, J.C., and Hulman, M.: Electronic transport in composites of graphite oxide with carbon nanotubes, Carbon 72 (2014) 224-232. (Not IEE SAS)

1. Han, Z.J.: NPG Asia Mater. 6 (2014) e140.
2. Kumar, R.: IET Circuits Dev. Systems 9 (2015) SI392.
3. Maarouf, A.A.: Carbon 102 (2016) 74.
4. Fan, M.: Green Chem. 18 (2016) 1731.
5. Al-Jumaili, A.: Materials 10 (2017) 1066.
6. Kharissova, O.V.: Industr. Engn. Chem. Res. 58 (2019) 3921.
#     7. Loganathan, A.: Rasayan J. Chem. 12 (2019)1710.
8. Karachevtsev, V.A.:Low Temp. Phys. 45 (2019) 1109.
9. Kurnosov, N.V.:Low Temp. Phys. 46 (2020) 346.
10. Glamazda, A. Y.: Physica E 124 (2020) 114279.
#   11. Loganathan, A.: Asian J. Chem. 32 (2020)  528.
12. Kurnosov, N.: Springer Proc. in Phys. 240 (2020) 79.
13. Ashraf, M.: Chem.-Europ. J. 27 (2021) 6973.

Meško, M., Vretenár, V., Kotrusz, P., Hulman, M., Šoltýs, J., and Skákalová, V.: Carbon nanowalls synthesis by means of atmospheric dcPECVD method, Phys. Status Solidi B 249 (2012) 2625–2628. (Not IEE SAS)

1. Bo, Z.: Phys. Status Solidi B 251 (2014) 155.
2. Zhang, X.: Phys. Status Solidi B 251 (2014) 829.
3. Mishin, M.V.: Russian J. General Chem. 85 (2015) 1209.
4. Zou, H.H.: Composites B 73 (2015) 57.
5. Bo, Z.: Phys. Status Solidi B 252 (2015) 2236.
6. Michniak, P.: NANOCON 2015. P. 143.
7. Li, M.: Advanced Sci 3 (2016) 1600003.
8. Bo, Z.: Phys. Status Solidi B 254 (2017) 1600804.
9. Vesel, A.: Materials 12 (2019) 2968.
10. Li, L.: Applied Phys. Lett. 115 (2019) 081101.
11. Jasek, O.: Diamond Related Mater. 105 (2020) 107798.
12. Sobczyk, A.T.: Applied Sci-Basel 11 (2021) 5845.
13. Vesel, A.: Nanomater. 12 (2022) 246.
14. Maksimovskii, E.A.: J. Structural Chem. 63 (2022) 1180.
15. Sahoo, S.: J. Energy Storage 53 (2022) 105212.
16. Singh, K.: J. Mater. Res. Technol.-JMR&T 24 (2023) 8572.
17. Tsukamoto, H.: J. Comp. Mater. 57 (2023) 1223.
18. Nixon, E.J.: Food Chem. 409 (2023) 135324.
19. Meher, B.S.: J. Mater. Engn. Performance 32 (2023) 3755.

Bandini, M., Eichholzer, A., Kotrusz, P., Tragni, M., Troisi, S., and Umani-Ronchi, A.: Ligand-free silver(i)-catalyzed intramolecular friedel–crafts alkylation of arenes with allylic alcohols Adv. Synth. Catal. 351 (2009) 319-324. (Not IEE SAS)

1. Zhang, X.X.: Organ. Biomolecul. Chem. 7 (2009) 4186.
2. Huang, W.: Tetrahedron 65 (2009) 3603.
3. Zhang, M.: Adv. Synth. Catal. 351 (2009) 1488.
4. Antoniotti, S.: SYNLETT (2010) 2973.
5. Sanz, R.: Europ. J. Organic Chem. 2010 (2010) 7027.
6. Nemoto, T.: Organic Lett. 12 (2010) 5020.
7. McCubbin, J.A.: J. Organic Chem. 75 (2010) 959.
8. Rueping, M.: Beilstein J. Organic Chem. 6 (2010) 6.
9. Niggemann, M.: Angewandte Chemie-Inter. Ed. 49 (2010) 3684.
10. Yeh, M.C.P.: Organometall. 29 (2010) 160.
11. Dang, T.T.: J. Organic Chem. 76 (2011) 9353.
12. Chen, G.Q.: SYNLETT (2011) 2713.
13. Wu, YC.: Adv. Synth. Catal. 353 (2011) 907.
14. Wei, B.M.: Chinese J. Organic Chem. 31 (2011) 392.
15. Emer, E.: Europ. J. Organic Chem. 2011 (2011) 647.
16. Chatterjee, P.N.: Tetrahedron 68 (2012) 3776.
17. Mothe, SR.: Chem.-A Europ. J. 18 (2012) 6133.
18. Hutait, S.: Europ. J. Organic Chem. 2012 (2012) 2453.
19. Pennell, MN.: Chem.-A Europ. J. 18 (2012) 4748.
20. Rao, Y.: Organ. Biomolecul. Chem. 11 (2013) 6029.
21. Maity, A.K.: Tetrahedron 69 (2013) 942.
22. Zhang, X.X.: Chinese J. Organic Chem. 35 (2015) 2049.
23. Vergara, A.P.: J. Chilean Chem. Soc 60 (2015) 3069.
24. Naveen, N.: Adv. Synth. Catal. 357 (2015) 1463.
25. Zhang, F.Z.: J. Organic Chem. 80 (2015) 1107.
26. Zhang, X.: Sci Synthesis 95 (2016).
27. Yuan, BF.: New J. Chem. 42 (2018) 15618.
28. Devi, N.R.: Synthesis-Stuttgart 52 (2020) 1425.
29. Nanda, S.K.: Chem.-A Europ. J. 27 (2021) 15571.
30. Nanda, S.K.: CHEMISTRYSELECT 6 (2021) 8511.
31. Rahmatpour, A.: Tetrahedron 95 (2021) 132341.

Bandini, M., Eichholzer, A., Kotrusz, P., and Umani-Ronchi, A.: Highly efficient molybdenum(II)-catalyzed intramolecular allylic alkylation of arenes, Adv. Synth. Catal. 350 (2008) 531-536. (Not IEE SAS)

1. Yamamoto, Y.: Chem.-A Europ. J. 14 (2008) 10705.
2. Huang, W.: Tetrahedron 65 (2009) 3603.
3. Medeiros, M.R.: Organic Lett. 12 (2010) 3222.
4. Xu, LW.: Adv. Synth. Catal. 352 (2010) 1441.
5. Rueping, M.: Beilstein J. Organic Chem. 6 (2010) 6.
6. Wu, YC.: Adv. Synth. Catal. 353 (2011) 907.
7. Emer, E.: Europ. J. Organic Chem. 2011 (2011) 647.
8. Holzwarth, M.S.: CHEMCATCHEM 5 (2013) 1650.
9. Bruno, S.M.: J. Organomet. Chem. 799-800 (2015) 179.
10. Zhang, X.: Sci Synthes. (2016) 95.
11. Zhang, W.: Tetrahedron 73 (2017) 4076.
12. Xu, G.Q.: Organometall. 38 (2019) 4003.
13. Jiang, X.D.: Organic Lett. 21 (2019) 608.

Cozzi, P.G. and Kotrusz, P.: Highly enantioselective addition of Me2Zn to aldehydes catalyzed by ClCr(Salen), J. American Chem. Soc 128 (2006) 4940-4941. (Not IEE SAS)

1. Hatano, M.: J. Organic Chem. 71 (2006) 6474.
2. Kowalczyk, R.: Tetrahedron-Asymm. 18 (2007) 2581.
3. Blay, G.: J. Molecul. Catal. A 276 (2007) 235.
4. Jammi, S.: Tetrahedron-Asymm. 18 (2007) 2016.
5. Liu, S.L.: Organic Lett. 9 (2007) 2965.
6. Mellah, M.: J. Molecul. Catal. A 272 (2007) 20.
7. Sokeirik, Y.S.: Organic Lett. 9 (2007) 1927.
8. Bisai, A.: Tetrahedron 63 (2007) 598.
9. Hui, X.P.: Chirality 19 (2007) 10.
10. Tosa, M. I.: Tetrahedron-Asymm. 19 (2008) 2068.
11. Tosa, M.: Tetrahedron-Asymm. 19 (2008) 1844.
12. Rodriguez-Escrich, S.: J. Organic Chem. 73 (2008) 5340.
13. Niu, Y.-N.: Tetrahedron-Asymm. 19 (2008) 912.
14. Li, G.-Q.: Tetrahedron-Asymm. 19 (2008) 816.
15. Wang, MC.: J. Organic Chem. 73 (2008) 168.
16. Sokeirik, Y.S.: Chem.-An Asian J. 3 (2008) 1850.
17. Jeyakumar, K.: Catal. Comm. 10 (2009) 1948.
18. Jaworska, M.: Applied Catal. A 357 (2009) 150.
19. Wang, M.-C.: Tetrahedron-Asymm. 20 (2009) 288.
20. Kowalczyk, R.: J. Organic Chem. 74 (2009) 753.
21. Zulauf, A.: Chem. Comm. (2009) 6574.
22. Akai, S.: Organic Lett. 12 (2010) 4900.
23. Matsuo, J.: Tetrahedron 66 (2010) 6062.
24. Zulauf, A.: Chem.-A Europ. J. 16 (2010) 11108.
25. Zulauf, A.: Dalton Trans. 39 (2010) 6911.
26. Fernandez-Mateos, E.: Europ. J. Organic Chem. 2011 (2011) 6851.
27. Hatano, M.: Tetrahedron 67 (2011) 4417.
28. Binder, C.M.: Organic Prepar. Proced. Inter. 43 (2011) 139.
29. Chinkov, N.: Angewandte Chemie-Inter. Ed. 50 (2011) 2957.
30. Wolf, C.: Chem. Comm. 47 (2011) 3339.
31. Cheng, Y.N.: Chem.-An Asian J. 7 (2012) 2921.
32. Infante, R.: Synthes.-Stuttgart 44 (2012) 1343.
33. Zilbeyaz, K.: Tetrahedron-Asymm. 23 (2012) 594.
34. Kang, S.Y.: Europ. J. Organic Chem. 2012 (2012) 1703.
35. Zulauf, A.: New J. Chem. 36 (2012) 1399.
36. Lihammar, R.: J. Organic Chem. 78 (2013) 12114.
37. Kleman, P.: Chem.-A Europ. J. 19 (2013) 16209.
38. Escorihuela, J.: Tetrahedron 69 (2013) 551.
39. Lumbroso, A.: Angewandte Chemie-Inter. Ed. 52 (2013) 1890.
40. Kleman, P.: ACS Catal. 4 (2014) 4398.
41. Panahi, F.: Adv. Synth. Catal. 357 (2015) 1211.
42. Li, F.: J. Organic Chem. 80 (2015) 3538.
43. Ferreira, D.S.P.: J. Molecul. Catal. B 126 (2016) 37.
44. Escorihuela, J.: Organ. Biomolecul. Chem. 14 (2016) 11125.
45. Veguillas, M.: Tetrahedron-Asymm. 27 (2016) 648.
46. Sola, R.: Molecules 23 (2018) 961.
47. Shaw, S.: Chem. Rev. 119 (2019) 9381.
48. Dandachi, H.: Vietnam J. Chem. 58 (2020) 29.
49. Papadopulu, Z.: Organic Lett. 23 (2021) 438.

Mečiarová, M., Toma, S., and Kotrusz, P.: Michael addition of thiols to α-enones in ionic liquids with and without organocatalysts, Organic Biomolecul. Chem. 4 (2006) 1420-1424. (Not IEE SAS)

1. Ramachary, D.B.: Tetrahedron Lett. 47 (2006) 7689.
2. Lacoste, Eric.: SYNLETT (2006) 1973.
3. Zhao, Y.: SYNLETT (2007) 1529.
4. Xu, J.M.: Europ. J. Organic Chem. 2007 (2007) 1798.
5. Durand, J.: Comptes Rendus Chimie 10 (2007) 152.
6. Xu, J.M.: Tetrahedron 63 (2007) 986.
7. Cozzi, P.G.: Coll. Czechoslov. Chem. Comm. 72 (2007) 1046.
8. Jereb, M.: Chem.-A Europ. J. 13 (2007) 9384.
9. Paczal, A.: Monatshefte Chemie 138 (2007) 1115.
10. Sharma, A.: Adv. Synth. Catal. 350 (2008) 2910.
11. Suresh, P.: Tetrahedron-Asymm. 19 (2008) 2037
12. Sarathi, P.A.: Bull. Korean Chem. Soc 29 (2008) 790.
13. Gruttadauria, M.: Chem. Soc Rev. 37 (2008) 1666.
14. Firouzabadi, H.: Tetrahedron 65 (2009) 5293.
15. Ying, A.G.: Tetrahedron Lett. 50 (2009) 1653.
16. Vale, J.A.: SYNLETT (2009) 75.
17. Kumar, A.: J. Sulfur Chem. 30 (2009) 570.
18. Mase, N.: SYNLETT (2010) 2340.
19. Riadi, Y.: Lett. Org. Chem. 7 (2010) 269.
20. Sarda, S.R.: 40 (2010) 2178.
21. Keglevich, G.: Current Organic Chem. 15 (2011) 3824.
22. Alza, E.: Chem.-A Europ. J. 17 (2011) 11585.
23. Movassagh, B.: Chinese Chem. Lett. 22 (2011) 1179.
24. Liu, Y.X.: Chinese J. Catal. 32 (2011) 1295.
25. Dalpozzo, R.: Symmetry-Basel 3 (2011) 84.
26. Chen, X.: Ionic Liquids (2011) 305.
27. Sarkar, A.: Chem. Comm. 47 (2011) 4538.
28. Abbasi, M.: Tetrahedron Lett. 53 (2012) 3683.
29. Palacio, C.: Chem. Comm. 48 (2012) 2849.
30. Wong, W.L.: Canad. J. Chem. 90 (2012) SI 1.
31. Guha, C.: J. Chem. Sci 125 (2013) 1463.
32. Priede, E.: SYNLETT 25 (2014) 2447.
33. Chauhan, P.: Chem. Rev. 114 (2014) 8807.
34. Zgrzeba, A.: RSC Adv. 5 (2015) 100354.
35. Perin, G.: CHEMISTRYSELECT 1 (2016) 205.
36. Shimizu, A.: Bull. Chem. Soc Japan 16 (2016) 61.
37. Rizzo, C.: RSC Adv. 6 (2016) 58477.
38. Bahekar, S.P.: Chem.Select 2 (2017) 9326.
39. Lauzon, S.: Europ. J. Organic Chem. 2018 (2018) 4536.
40. Radai, Z.: Current Organic Chem. 22 (2018) 533.
41. Zhong, Y.: J. Mater. Chem. C 7 (2019) 256.
42. Tamboli, R.S.: Chem.Select 4 (2019) 1138.
43. Makso, L.: CHEMISTRYSELECT 7 (2022) e202200967.
#       44. Marini, F.: Organochalcogen Compounds: Synthesis, Catalysis and New Protocols with Greener Perspectives. Elsevier 2022, pp. 147-192. ISBN 978-0-12-819449-2
45. Ratnani, S.: J. Iran. Chem. Soc 20 (2023) 495.
46. Zhang, R.A.: Organic Biomolecul. Chem. 21 (2023) 1163.

Kotrusz, P. and Toma, Š.: L-proline catalyzed michael additions of thiophenols to α,β unsaturated compounds, particularly α-enones, in the ionic liquid [bmim]PF6, Molecules 11 (2006) 197-205. (Not IEE SAS)

1. Zheng X.: Progress Chem. 20 (2008) 1675.
2. Suresh, P.: Tetrahedron-Asymm. 19 (2008) 2037.
3. Kumar, A.: Tetrahedron Lett. 50 (2009) 7024.
4. Samai, S.: Tetrahedron 65 (2009) 10155.
5. Indumathi, S.: Europ. J. Medicin. Chem. 44 (2009) 4978.
6. Chu, CM.: Tetrahedron 65 (2009) 3878.
7. Hui, X.P.: Synthet. Comm. 39 (2009) 676.
8. Shi, C.: J. Combinat. Chem. 12 (2010) 430.
9. Zhong, T.: Chinese J. Organic Chem. 30 (2010) 981.
10. Mukhopadhyay, C.: Tetrahedron Lett. 51 (2010) 1797.
11. Li, Y.: J. Combinat. Chem. 12 (2010) 231.
12. Liu Y.: Chinese J. Catal. 32 (2011) 1295.
13. Zare, L.: Chinese Chem. Lett. 22 (2011) 531.
14. Shi, C.L.: J. Heterocyc. Chem. 48 (2011) 351.
15. Bhowmik, S.: RSC Adv. 1 (2011) 1237.
16. Choudhary, G.: Green Chem. 13 (2011) 276.
17. Rajesh, S.M.: Green Chem. 13 (2011) 3248.
18. Wang, H.: Organic Lett. 14 (2012) 4598.
19. Heravi, M.M.: J. Chem. Sci 124 (2012) 865.
20. Liu, X.: Synthet. Comm. 42 (2012) 75.
21. Shi, C.-L.: J. Heterocyc. Chem. 49 (2012) 125.
22. Zhang, F.: Synthesis-Stuttgart 45 (2013) 3007.
23. Nasreen, A.: Tetrahedron Lett. 54 (2013) 3797.
24. Mofakham, H.: J. Iran. Chem. Soc 10 (2013) 307.
25. Gunasekaran, P.: RSC Adv. 3 (2013) 8318.
26. Anderson, J.C.: Tetrahedron 70 (2014) 9337.
27. Chauhan, P.: Chem. Rev. 114 (2014) 8807.
28. Darbem, M.P.: Tetrahedron Lett. 55 (2014) 5179.
29. Climent, M.J.: Applied Catal. A 481 (2014) 27.
30. Brahmachari, G.: RSC Adv. 4 (2014) 7380.
31. Kamal, A.: RSC Adv. 4 (2014) 46369.
32. Naqvi, T.: Chiang Mai J. Sci 42 (2015) 877.
33. Swain, SP.: Adv. Synth. Catal. 357 (2015) 2644.
34. Fu, L.: J. Heterocyc. Chem. 52 (2015) 1075.
35. Mohapatra, S.: Res. Chem. Intermed. 41 (2015) 4545.
36. Seydimemet, M.: Tetrahedron 72 (2016) 7599.
37. Baichurin, R.I.: Russian J. Org. Chem. 52 (2016) 818.
38. Perin, G.: Chem.Select 1 (2016) 205.
39. Dilauro, G.: Comptes Rendus Chimie 20 (2017) 617.
40. Deb, M.L.: Tetrahedron Lett. 59 (2018) 4430.
41. Sahu, P.K.: ACS Omega 3 (2018) 15035.
42. Keshavarz, M.: Molecules 23 (2018) 330.
43. Katla, R.: Chem.Select 4 (2019) 13304.
44. Bayannavar, P.K.: Synthet. Comm. 49 (2019) 2005.
45. Kaurav, M.S.: RSC Adv. 9 (2019) 3755.
46. Rahman, I.: Organ. Biomolecul. Chem. 18 (2020) 6514.
47. Jha, A.M.: Heterocyc. Lett. 11 (2021) 31.
48. Manjunatha, B.: J. Molecul. Struct. 1249 (2022) 131642.
49. Al-Rooqi, M.M.: J. Molecul. Struct. 1268 (2022) 133719.
50. Kadam, P.R.: Results Chem. 4 (2022) 100303.
51. Thorat, B.R.: Combinat. Chem. High Throughput Screen. 26 (2023) 1108.

Kotrusz, P. and Toma, Š.: L-proline catalysed Michael additions of different active methylene compounds to α-enones in ionic liquid, Arkivoc 2006 (2006) 100-109. (Not IEE SAS)

1. Kumar, A.: Tetrahedron 63 (2007) 11086.
2. Karade, N.N.: Chinese J. Chem. 25 (2007) 1686.
3. Kumar, A.: Tetrahedron Lett. 48 (2007) 3887.
4. Kumar, A.: Tetrahedron 63 (2007) 1946.
5. Karade, N.N.: Lett. Org. Chem. 4 (2007) 16.
6. Zare, A.: Arkivoc (2007) 105.
7. Hasaninejad, A.: J. Chilean Chem. Soc 53 (2008) 1663.
8. Plaquevent, J.-C.: Chem. Rev. 108 (2008) 5035.
9. Zheng X.: Progress Chem. 20 (2008) 1675.
10. Shi, C.: J. Chem. Res. (2008) 534.
11. Kumar, A.: Tetrahedron 64 (2008) 3477.
12. Kotsuki, H.: Heterocyc. 75 (2008) 757.
13. Shi, CL.: Tetrahedron 64 (2008) 2425.
14. Zare, A.: J. Iran. Chem. Soc 5 (2008) 100.
15. Shi, C.-L.: Austral. J. Chem. 61 (2008) 547.
16. Paike, V.V.: Organic Lett. 11 (2009) 5586.
17. Pansare, SV Organ. Biomolecul. Chem. 8 (2009) 319.
18. Roca-Lopez, D.: Tetrahedron-Asymm. 21 (2010) 2561.
19. Shi, C.: J. Combinat. Chem. 12 (2010) 430.
20. Guo, S.: Chinese J. Chem. 28 (2010) 811.
21. Li, Y.: J. Combinat. Chem. 12 (2010) 231
22. Shi, C.: J. Chem. Res. (2011) 585.
23. Yoshida, M.: Symmetry-Basel 3 (2011) 155.
24. Rajanarendar, E.: Indian J. Chem. Sec. B 50 (2011) 751.
25. Shi, C.-L.: J. Heterocyc. Chem. 48 (2011) 351.
26. Wang, H.: Organic Lett. 14 (2012) 4598.
27. Heravi, M.M.: J. Chem. Sci 124 (2012) 865.
28. Rajanarendar, E.: Tetrahedron Lett. 53 (2012) 2909.
29. Al-Momani, Lo’ay A.: Arkivoc 101 (2012) 101.
30. Jain, S.: J. Serbian Chem. Soc 77 (2012) 1345.
31. Liu, X.: Synthet. Comm. 42 (2012) 75.
32. Oge, A.: Turkish J. Chem. 36 (2012) 137.
33. Shi, C.-L.: J. Heterocyc. Chem. 49 (2012) 125.
34. Zhang, F.: Synthesis-Stuttgart 45 (2013) 3007.
35. Reddy, M. S.: Toxicol. Environ. Chem. 95 (2013) 1518.
36. Moirangthem, N.: Indian J. Chem. Sec. B 52 (2013) 937.
37. Brahmachari, G.: RSC Adv. 4 (2014) 7380.
38. Kamal, A.: RSC Adv. 4 (2014) 46369.
39. Sahu, P.K.: J. Indian Chem. Soc 92 (2015) 169.
40. Fu, L.: J. Heterocyc. Chem. 52 (2015) 1075.
41. Rao, L.C.: Helvetica Chim. Acta 98 (2015) 978.
42. Gunduz, H.: Tetrahedron 73 (2017) 4335.
43. Bhattacharjee, D.: Tetrahedron 73 (2017) 3497.
44. Sahu, P.K.: ACS Omega 3 (2018) 15035.
45. Kaurav, M.S.: RSC Adv. 9 (2019) 3755.
46. Reddy, M.M.: Chem.Select 5 (2020) 4816.
47. Tasqeeruddin, S.: Lett. Org. Chem. 17 (2020) 157.
48. Zare, L.: Chinese Chem. Lett. 32 (2021) 531.
49. Gogoi, A.: Current Organic Chem. 25 (2021) 1566.
50. Kadam, P.R.: Results Chem. 4 (2022) 100303.
51. Sukanya, S. H.: J. Molecul. Struct. 1247 (2022) 131324.
52. Thorat, B.R.: Combinat. Chem. High Throughput Screen. 26 (2023) 1108.

Kotrusz, P., Alemayehu, S., Toma, Š., Schmalz, H.-G., and Adler, A.: Enantioselective organocatalysis in ionic liquids: Addition of aliphatic aldehydes and ketones to diethyl azodicarboxylate, Europ. J. Organic Chem. (2005) 4904-4911. (Not IEE SAS)

1. Liu, X.H.: J. Zhejiang Univ.-Sci B 9 (2008) 990.
2. Plaquevent, J.C.: Chem. Rev. 108 (2008) 5035.
3. Chen, Q.A.: Tetrahedron Lett. 50 (2009) 6866.
4. Shah, J.: Synthesis-Stuttgart (2009) 3975.
5. Kosmrlj, J.: SYNLETT ( 2009) 2217.
6. Li, J.Y.: Europ. J. Organic Chem. 2009 (2009) 132.
7. Pihko, P.M.: Asymmet. Organocatal. 291 (2009) 29.
8. Ding, X.O.: Tetrahedron Lett. 51 (2010) 6105.
9. Liu, P.M.: Europ. J. Organic Chem. 2010 (2010) 5705.
10. Fu, J.Y.: Tetrahedron Lett. 51 (2010) 4870.
11. Shigenaga, A.: Tetrahedron 66 (2010) 7367.
12. Gosiewska, S.: Tetrahedron Lett. 51 (2010) 4214.
13. Xu, LJ.: Progress Chem. 22 (2010) 1254.
14. Vilaivan, T.: Molecules 15 (2010) 917.
15. Fu, J.Y.: Organ. Biomolecul. Chem. 8 (2010) 4524.
16. Kanzian, T.: Chem.-A Europ. J. 16 (2010) 11670.
17. Liu, P.M.: Europ. J. Organic Chem. 2010 (2010) 42.
18. Zlotin, S.G.: Russian Chem. Rev. 79 (2010) 543.
19. Guo, H.M.: Green Chem. 8 (2006) 682.
20. Alladoum, J.: J. Organic Chem. 73 (2008) 9771.
21. Fu, J.Y.: J. Organic Chem. 76 (2011) 4661.
22. Hallett, J.P.: Chem. Rev. 111 (2011) 3508.
23. Vallribera, A.: Current Organic Chem. 15 (2011) 1539.
24. Beattie, C.: Molecules 16 (2011) 3420
25. Aitken, D.J.: SYNLETT ( 2011) 712.
26. Mailhol, D.: Adv. Synth. Catal. 354 (2012) 3523.
27. Fan, XY.: Adv. Synth. Catal. 354 (2012) 2971.
28. Xu, X.L.: Chinese J. Organic Chem. 32 (2012) 1024.
29. Aitken, D.J.: Organ. Biomolecul. Chem. 10 (2012) 5045.
30. Hernandez, J.G.: Chem. Comm. 48 (2012) 5396.
31. Secci, F.: Molecules 18 (2013) 15541.
32. Frongia, A.: Chem. Comm. 49 (2013) 8812.
33. Koz, G.: Zeitsch. Naturforschung Sec. B 68 (2013) 57.
34. Siyutkin, D.E.: Comprehen. Enantioselective Organocatal.: Catalysts, Reactions, And Appl., Vols. 1-3 (2013) 617.
35. Wang, C.: RSC Adv. 3 (2013) 8796.
36. Msutu, A.: Tetrahedron Lett. 55 (2014) 2295.
37. Frongia, A.: Asian J. Organ. Chem. 3 (2014) SI378.
38. Aitken, D.J.: Adv. Synthes. Catal. 356 (2014) 941.
39. Wang, C.: Inter. J. Molecul. Sci 15 (2014) 1284.
40. Zhirov, A.M.: Russian Chem. Rev. 83 (2014) 502.
41. Melis, N.: Europ. J. Organic Chem. 2015 (2015) 4358.
42. Frongia, A.: Comptes Rendus Chimie 18 (2015) 456.
43. Weng, J.: Tetrahedron Lett. 57 (2016) 2554.
44. Ferreira, J.: Organ. Biomolecul. Chem. 14 (2016) 1545.
45. Lang, JH.: Chem.-A Europ. J. 23 (2017) 12714.
46. Gurka, A.A.: Struct. Chem. 28 (2017) 415.
47. Veverkova, E.: Europ. J. Organic Chem. 2017 (2017) 1191.
48. Karimi, B.: CHEMCATCHEM 10 (2018) 3173.
49. Gogoi, A.: Current Organic Chem. 25 (2021) 1566.
50. Nishimura, K.: Organic Lett. 24 (2022) 7685.
51. Yeo, H.M.: CHEMISTRYSELECT 8 (2023) 202300060.

Kotrusz, P., Toma, S., Schmalz, H.-G., and Adler, A.: Michael additions of aldehydes and ketones to β-nitrostyrenes in an ionic liquid, Europ. J. Organic Chem.  (2004) 1577-1583. (Not IEE SAS)

1. Shah, J.: Synthesis-Stuttgart (2009) 3975.
2. Xu, D.Z.: Europ. J. Organic Chem. 2009 (2009) 4848.
3. Widianti, T.: Tetrahedron-Asymm. 21 (2010) 1861.
4. Xu, L.J.: Progress Chem. 22 (2010) 1254.
5. Liu, J.: Chirality 22 (2010) 432.
6. Ni, B.K.: Chem.-A Europ. J. 16 (2010) 4426.
7. Zlotin, S.G.: Russian Chem. Rev. 79 (2010) 543.
8. Keglevich, G.: Current Organic Chem. 15 (2011) 3824.
9. Jentzsch, KI.: J. Organic Chem. 76 (2011) 7065.
10. Samai, S.: Tetrahedron 67 (2011) 5935.
11. Liu, Y.X.: Chinese J. Catal. 32 (2011) 1295.
12. Aitken, D.J.: SYNLETT ( 2011) 712
13. Omar, E.M.: Lett. Org. Chem. 8 (2011) 170.
14. Anwar, S.: Tetrahedron 67 (2011) 1171.
15. Gavin, D.P.: Arkivoc (2011) 407.
16. Su, Z.: Organ. Biomolecul. Chem. 9 (2011) 6402.
17. Mailhol, D.: Adv. Synth. Catal. 354 (2012) 3523.
18. Kasaplar, P.: Adv. Synth. Catal. 354 (2012) 2905.
19. Raghuvanshi, R.S.: J. Indian Chem. Soc 89 (2012) 679.
20. Aitken, D.J.: Organ. Biomolecul. Chem. 10 (2012) 5045.
21. Hernandez, J.G.: Chem. Comm. 48 (2012) 5396.
22. Jain, S.: J. Serbian Chem. Soc 77 (2012) 1345.
23. Ma, S.J.: Organ. Biomolecul. Chem. 10 (2012) 3721.
24. Yang, H Organ. Biomolecul. Chem. 10 (2012) 3229.
25. Secci, F.: Molecules 18 (2013) 15541.
26. Chowdhury, R.: Europ. J. Organic Chem. 2013 (2013) 6167.
27. Narancic, T.: Bioresource Technol. 142 (2013) 462.
28. Narayanaperumal, S.: Ultrason. Sonochem. 20 (2013) 793.
29. Siyutkin, D.E.: Comprehen. Enantioselective Organocatal.: Catalysts, Reactions, And Appl., Vols. 1-3 (2013) 617.
30. Su, Z.: Europ. J. Organic Chem. 2013 (2013) 1706.
31. Horitsugi, N.: Asian J. Organ. Chem. 3 (2014) SI445.
32. Gonczi, K.: Thermochim. Acta 580 (2014) 46.
33. Doherty, S.: RSC Catal. Ser. 15 (2014) 44.
34. Zheng, Y.S.: Organic Lett. 17 (2015) 4240.
35. Yang, D.X.: Chem.-A Europ. J. 21 (2015) 1458.
36. Xia, A.B.: New J. Chem. 39 (2015) 355.
37. Phillips, A.M.: Current Organ. Synthes. 13 (2016) 687.
38. Rizzo, C.: RSC Adv. 6 (2016) 58477
39. Tukhvatshin, R.S.: ACS Catal. 7 (2017) 2981.
40. Sahin, B.: Synthet. Comm. 47 (2017) 1090.
41. Karimi, B.: CHEMCATCHEM 10 (2018)3173
42. Ramirez-Jimenez, R.: J. Mater. Chem. A 6 (2018) 12637.
43. Wen, T.: Chinese J. Organic Chem. 39 (2019) 3162.
44. Pomaranski, P.: Synthesis-Stuttgart 51 (2019) 3356.
45. Omar, E.M.: Synthet. Comm. 49 (2019) 1578.
46. Ranaivoarimanana, N.J.: Molecules 24 (2019) 1231.
47. Wen, T.: Chinese J. Organic Chem. 39 (2019) 3162.
48. Kristofikova, D.: CHEMSUSCHEM 13 (2020) 2828.
49. Wang, M.: SYNLETT 32 ( 2021) 1253.
50. Gogoi, A.: Current Organic Chem. 25 (2021) 1566.
51. Ganesan, D.: HETEROCYC. 105 (2022) 369.

Kotrusz, P., Kmentová, I., Gotov, B., Toma, Š., and Solčániová, E.: Proline-catalysed asymmetric aldol reaction in the room temperature ionic liquid [bmim]PF6, Chem. Comm. 21 (2002) 2510-2511. (Not IEE SAS)

1. Davey, P.N.: Green Chem. 7 (2005) 224.
2. Ding, X.O.: Tetrahedron Lett. 51 (2010) 6105.
3. Ban, S.R.: Europ. J. Organic Chem. 2011 (2011) 6413.
4. Keglevich, G.: Current Organic Chem. 15 (2011) 3824.
5. Zhang, L.: J. Brazil. Chem. Soc 22 (2011) 1736.
6. Liu, Y.X.: Chinese J. Catal. 32 (2011) 1295.
7. Hallett, J.P.: Chem. Rev. 111 (2011) 3508.
8. Hu, S.Q.: Progress Chem. 23 (2011) 731.
9. Aitken, D.J.: SYNLETT (2011) 712.
10. Yong, F.F.: Synthet. Comm. 41 (2011) 1293.
11. Zhang, L.: Catal. Sci Technol. 1 (2011)  507.
12. Shen, J.F.: Adv. Synth. Catal. 354 (2012) 3311.
13. Giacalone, F.: Chem. Soc Rev. 41 (2012) 2406
14. Hernandez, J.G.: Chem. Comm. 48 (2012) 5396.
15. Ramachary, D.B.: Organ. Biomolecul. Chem. 10 (2012) Iss. 26.
16. Wang, W.: Dalton Trans. 41 (2012) 5715.
17. Xu, N.: Synthet. Comm. 42 (2012) 1559.
18. Thingom, B.: Indian J. Chem. B 52 (2013) 929.
19. Cota, I.: Ionic Liquids – New Aspects for the Future (2013) 365.
20. Kong, Y.: Green Chem. 15 (2013) 2422.
21. Kumar, A.: RSC Adv. 3 (2013) 603.
22. Siyutkin, D.E.: Comprehen. Enantioselective Organocatal.: Catalysts, Reactions, And Appl., Vols. 1-3 (2013) 617.
23. Wang, C.: RSC Adv. 3 (2013) 8796.
24. Gonzalez, L.: Europ. J. Organic Chem. 2014 (2014) 5356.
25. Banon-Caballero, A.: Mini-Rev. Organ. Chem. 11 (2014) 118.
26. Doherty, S.: RSC Catal. Ser. 15 (2014) 44.
27. Bartok, M.: Catal. Rev.-Sci Engn. 57 (2015) 192.
28. Porcar, R.: ACS Sustainable Chem. Engn. 4 (2016) 6062.
29. Fiala, D.: Current Sci 110 (2016) 1524.
30. Lou, L.L.: Catal. Today 264 (2016) 109.
31. Khandelwal, S.: Current Organocat. 3 (2016) 176.
32. Kumar, G.V.: Synthet. Comm. 46 (2016) 483.
33. Luridiana, A.: Organ. Biomolecul. Chem. 14 (2016) 3394.
34. Liu, J.: Synthesis-Stuttgart 49 (2017) 960.
35. Campisciano, V.: Chem. Record 17 (2017) 918.
36. Heravi, M.M.: Tetrahedron-Asymm. 28 (2017) 587.
37. Obregon-Zuniga, A.: Organic Lett. 19 (2017) 1108.
38. Yamashita, Y.: Chem. Soc Rev. 47 (2018) 4388.
39. Sarkale, A.M.: J. Organic Chem. 83 (2018) 4167.
40. Akgul, D.: J. Molecul. Graphics Modell. 88 (2019) 309.
41. Emma, M.G.: Catalysts 10 (2020) 649.
42. Kristofikova, D.: CHEMSUSCHEM 13 (2020) 2828.
43. Suzuki, N.: Lett. Org. Chem. 17 (2020) 717.
44. Wang, Y.: Green Chem. 23 (2021) 7773.
45. Juaristi, E.: Tetrahedron 88 (2021)
46. Inani, H.: Synthesis-Stuttgart 53 (2021) 2702.
47. Gogoi, A.: Current Organic Chem. 25 (2021) 1566.
48. Sun, ZY.: Catal. Sci Technol. 11 (2022)  4811.
49. Ardevines, S.: Catalysts  12 (2022) Iss. 1.
50. Deepa, S.: CHEMISTRYSELECT 8 (2023).
51. Thorat, B.R.: Combinat. Chem. High Throughput Screen. 26 (2023) 1108.