26. Z. Czakó, L. Juhász, Á. Kenéz, K. Czifrák, L. Somsák, T. Docsa, P. Gergely, S. Antus, Bioorg. Med. Chem., 17 (2009) 6838-6741. 27. Talan RS, Sanki AK, Sucheck SJ, CARBOHYDRATE RESEARCH 344 (2009) 2048-2050. 28. É. Bokor, T. Docsa, P. Gergely, L. Somsák, Bioorg. Med. Chem., 18 (2010) 1171-1180. 29. Somsák L., Bokor É., Czifrák K., Kónya B., Kun S., Tóth, M. Magy. Kém. Folyóirat, 116 (2010) 19-30. 30. Antus, S. Acta Pharm. Hung., 79 (2009) 143-167. 31. Antus, S. Acta Pharm. Hung., 80 (2010) 3-17. 32. Muehlberg, M., Jaradat, D. M. M., Kleineweischede, R., Papp, I., Dechtrirat, D., Muth, S., Broncel, M., Hackenberger, C. P. R., BIOORGANIC & MEDICINAL CHEMISTRY 18 (2010) 3679-3686. 33. Zhu, Deguang; Chen, Ruijiao; Liang, Haibo; Li, Sheng; Pan, Li; Chen, Xiaochuan Synlett (2010) 897-900. 34. Chrysina, E. D., Mini Rev. Med. Chem., 10 (2010) 1093-1101. 35. L. Somsák, C. R. Chimie 14 (2011) 211–223. 36. S. Kun, G. Z. Nagy, M. Tóth, L. Czecze, A. Nguyen Van Nienh, T. Docsa, P. Gergely, M.-D. Charavgi, P. V. Skourti, E. D. Chrysina, T. Patonay, L. Somsák, Carbohydr. Res., 346 (2011) 1427-1438. 37. Srivastava A, Varghese B, Loganathan D, Journal of Carbohydrate Chemistry 31 (2012) 31-47. 38. N.G. Oikonomakos, M. N. Kosmopoulou, D. D. Leonidas, E. D. Chrysina, C. Tiraidis, N. Bischler, K. E. Tsitsanou, S. E. Zographos, I. D. Kostas, and G. Eisenbrand (2006). Indirubin and indigo analogues as potential inhibitors of glycogenolysis: structural basis of glycogen phosphorylase inhibition. In Indirubin, the red shade of indigo (Meijer L., Guyard N., Skaltsounis L. & Eisenbrand G., eds) Editions “Life in Progress”, Station Biologique, Roscoff, Chapter 18, pp. 177-189. ISBN: 2- 9518029-0-0. http://www.sb-roscoff.fr/usr3151-editions/132-indirubin-.html 71. L. Somsák, K. Czifrák, E. Veres: Selective removal of 2,2,2-trichloroethyl- and 2,2,2-trichloroethoxycarbonyl protecting groups with Zn–N-methylimidazole in the presence of reducible and acid-sensitive functionalities Tetrahedron Lett., 45 (2004) 9095-9097. IF: 2.484 (2004) Cited by/Idézi: 1. Czifrak K, Szilagyi P, Somsak L, TETRAHEDRON-ASYMMETRY 16 (2005) 127-141. 2. Tokimoto H, Fukase K, TETRAHEDRON LETTERS 46 (2005) 6831-6832. 3. Law MC, Wong KY, Chan TH, JOURNAL OF ORGANIC CHEMISTRY 70 (2005) 10434-10439. 4. Vellemae E, Lebedev O, Sillard R, Maeorg U, JOURNAL OF CHEMICAL RESEARCH-S (2006) 685- 687. 5. Zeghida W, Demeunynck M., SYNTHESIS-STUTTGART (2007) 231-234. 6. Bongat AFG, Demchenko AV, CARBOHYDRATE RESEARCH 342 (2007) 374-406. 7. Braese, S.; Lesch, B.; Zimmermann, V. Science of Synthesis (2010), Volume Date 2009, 41, 543-612. 8. Pal APJ, Vankar YD, TETRAHEDRON LETTERS 51 (2010) 2519-2524. 9. Huang, C.-Y., Wang, N., Fujiki, K., Otsuka, Y., Akamatsu, M., Fujimoto, Y., Fukase, K., JOURNAL OF CARBOHYDRATE CHEMISTRY 29 (2010) 289-298. 10. Vellemae E, Stepanov V, Maeorg U, SYNTHETIC COMMUNICATIONS 40 (2010) 3397-3404. 11. Pal, A. P. J., Kadigachalam, P., Mallick, A., Doddi, V. R., Vankar, Y. D. ORGANIC & BIOMOLECULAR CHEMISTRY 9 (2011) 809-819. 12. Kim MR, Maheswara M, Do JY, BULLETIN OF THE KOREAN CHEMICAL SOCIETY 32 (2011) 664-672. 13. Jianbo Zhang, Jie Fu, Wenshuai Si, Xiaohu Wang, Zhongfu Wang, Jie Tang, Carbohydrate Research 346 (2011) 2290–2293. 72. R. Elek, L. Kiss, J.-P. Praly, L. Somsák: -D-Galactopyranosyl-thiohydroximates and D-galactopyranosylidene-spiro-oxathiazoles: 56
synthesis and enzymatic evaluation against E. coli D-galactosidase Carbohydr. Res., 340 (2005) 1397-1402. IF: 1.669 (2005) Cited by/Idézi: 1. Zhang, P.-Z., Li, X.-L., Chen, H., Li, Y.-N., Wang, R., TETRAHEDRON LETTERS 48 (2007) 7813- 7816. 2. L. Somsák, V. Nagy, S. Vidal, K. Czifrák, E. Berzsényi, J.-P. Praly, Bioorg. Med. Chem. Lett., 18 (2008) 5680-5683. 3. Li, X., Wang, R., Wang, Y., Chen, H., Li, Z., Ba, C., Zhang, J., TETRAHEDRON, 64 (2008) 9911- 9920. 4. V. Nagy, S. Vidal, K. M. Benltifa, E. Berzsényi, C. Teilhet, K. Czifrák, Gy. Batta, T. Docsa, P. Gergely, L. Somsák, J.-P. Praly, Bioorg. Med. Chem., 17 (2009) 5696-5707. 5. Benltifa, M., De Kiss, M., Isabel Garcia-Moreno, M., Ortiz Mellet, C., Gueyrard, D., Wadouachi, A., TETRAHEDRON-ASYMMETRY 20 (2009) 1817-1823. 6. Benltifa, M., Hayes, J. M., Vidal, S., Gueyrard, D., Goekjian, P. G., Praly, J.-P., Kizilis, G., Tiraidis, C., Alexacou, K.-M., Chrysina, E. D., Zographos, S. E., Leonidas, D. D., Archontis, G., Oikonomakos, N. G., BIOORGANIC & MEDICINAL CHEMISTRY 17 (2009) 7368-7380. 7. N. Felföldi, M. Tóth, E. D. Chrysina, M.-D. Charavgi, K.-M. Alexacou, L. Somsák,Carbohydr. Res., 345 (2010) 208-213. 73. K. Czifrák, P. Szilágyi, L. Somsák: Anomeric -azido acid (2-azido-2-deoxy-hept-2-ulopyranosonic acid) derivatives en route to peptides incorporating sugar amino acids Tetrahedron: Asymmetry, 16 (2005) 127-141. Meghívott cikk. IF: 2.429 (2005) Cited by/Idézi: 1. K. Czifrák, L. Kovács, K. E. Kövér, L. Somsák, Carbohydr. Res., 340 (2005) 2328-2334. 2. Dondoni A, Massi A, Sabbatini S, CHEMISTRY-A EUROPEAN JOURNAL 11 (2005) 7110-7125. 3. Benltifa, M.; Vidal, S.; Fenet, B.; Msaddek, M.; Goekjian, P. G.; Praly, J.-P.; Brunyánszki, A.; Docsa, T.; Gergely, P., European Journal of Organic Chemistry 2006, 4242-4256. 4. Murphy PV, Dunne JL, CURRENT ORGANIC SYNTHESIS 3 (2006) 403-437. 5. Norris P, CURRENT TOPICS IN MEDICINAL CHEMISTRY, 8 (2008) 101-113. 6. S. S. Kulkarni, J. Gervay-Hague Glycosyl Chlorides, Bromides, and Iodides in Handbook of Chemical Glycosylation (Ed. A. V. Demchenko), Wiley-VCH, 2008, pp. 59-93. 7. Aldhoun M, Massi A, Dondoni A, JOURNAL OF ORGANIC CHEMISTRY 73 (2008) 9565-9575. 8. K. Czifrák, L. Somsák, Carbohydr. Res., 344 (2009) 267-277. 9. Barghash RF, Massi A, Dondoni A, ORGANIC & BIOMOLECULAR CHEMISTRY 7 (2009) 3319- 3330. 10. Antus, S. Acta Pharm. Hung., (2010) 3-17. 11. Pal APJ, Vankar YD, TETRAHEDRON LETTERS 51 (2010) 2519-2524. 12. Pal, A. P. J., Kadigachalam, P., Mallick, A., Doddi, V. R., Vankar, Y. D. ORGANIC & BIOMOLECULAR CHEMISTRY 9 (2011) 809-819. 13. Czifrak, K., Gyollai, V., Koever, K. E., Somsak, L., CARBOHYDRATE RESEARCH, 346 (2011) 2104- 2112. 74. L. Somsák, V. Nagy, Zs. Hadady, N. Felföldi, T. Docsa, P. Gergely: Recent developments in the synthesis and evaluation of glucose analog inhibitors of glycogen phosphorylases as potential antidiabetic agents 57
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Total publications/Összes publiká
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5. L. Somsák, I. Romhányi, K. Pes
- Page 5 and 6: 26. P. M. Harrington, M. E. Jung, T
- Page 7 and 8: 5. S. H. Mahmoud, L. Somsák, I. Fa
- Page 9 and 10: 15. L. Somsák: A kapto-datív gyö
- Page 11 and 12: 9. S. D. Rychnovsky, J. P. Powers,
- Page 13 and 14: 15. T. W. Brandstetter, M. W. Worma
- Page 15 and 16: 3. J.-P. Praly, C. Di Stéfano, G.
- Page 17 and 18: 41. Capozzi, Giuseppe; Menichetti,
- Page 19 and 20: 34. Sipos Szabolcs; Jablonkai Istva
- Page 21 and 22: 32. L. Kiss, L. Somsák: Evaluation
- Page 23 and 24: 34. L. Somsák, J. Madaj, A. Wisnie
- Page 25 and 26: 9. Györgydeák Z, Thiem J, ADVANCE
- Page 27 and 28: 18. Lillelund VH, Jensen HH, Liang
- Page 29 and 30: 41. Gy. Kovács, K. Tóth, Z. Dinya
- Page 31 and 32: 45. L. Somsák, V. Nagy, T. Docsa,
- Page 33 and 34: 16. Marinov M, Minchev S, Stoyanov
- Page 35 and 36: 37. Agnihotri G, Misra AK, CARBOHYD
- Page 37 and 38: 106. Hélio A. Stefani, Nathália C
- Page 39 and 40: 43. L. Somsák, V. Nagy, S. Vidal,
- Page 41 and 42: 13. Benltifa, M., Hayes, J. M., Vid
- Page 43 and 44: 2. T. Docsa, B. Tóth, L. Somsák,
- Page 45 and 46: 16. K. Czifrák, Zs. Hadady, T. Doc
- Page 47 and 48: conditions without carbon tetrachlo
- Page 49 and 50: 44. Benltifa, M.; Vidal, S.; Fenet,
- Page 51 and 52: 106. Schoenemann, W., Gallienne, E.
- Page 53 and 54: 2. E.D. Chrysina, M.N. Kosmopoulou,
- Page 55: 70. Z. Györgydeák, Zs. Hadady, N.
- Page 59 and 60: 27. Benltifa, M., De Kiss, M., Isab
- Page 61 and 62: 31. Somsák L., Bokor É., Czifrák
- Page 63 and 64: 79. K. Czifrák, Zs. Hadady, T. Doc
- Page 65 and 66: Cited by/Idézi: 1. L. Somsák, V.
- Page 67 and 68: 85. L. Somsák, K. Czifrák, M. Tó
- Page 69 and 70: 12. Shahid I. Awan, Daniel B. Werz,
- Page 71 and 72: Bioorg. Med. Chem., 17 (2009) 4773-
- Page 73 and 74: IF: 1.898 (2010) Cited by/Idézi: 1
- Page 75 and 76: 106. M. Tóth, S. Kun, L. Somsák,
- Page 77 and 78: B) ÉRTEKEZÉSEK 1. Vízoldható r
- Page 79 and 80: D) MŰBÍRÁLATOK 1. Report on the