21. P. A. Chaloner, M. A. Esteruelas, F. Joó, L. A. Oro, Homogeneous Hydrogenation, Kluwer Academic Publishers, 1994, pp 202-203. 22. N. K. Singha, S. Sivaram, S. S. Talwar, Rubber Chem. Technol., 68 (1995) 281-286. 23. P A Chaloner, Handbook of Coord. Catal. in Org. Chem., London: Butterworths, 1985. 189 p. 24. F. Joó, L. Nádasdi, A. Bényei, D. J. Darensbourg, J. Organomet. Chem., 512 (1996) 44-50. 25. D. E. Bergbreiter, Y. S. Liu, Tetrahedron Lett., 38 (1997) 3703-3706. 26. D. E. Bergbreiter, Y. S. Liu, Tetrahedron Lett., 38 (1997) 7843-7846. 27. Nomura-K JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL 1998, 130, pp 1-28 28. Beller, Matthias; Krauter, Jurgen G. E. Aqueous-Phase Organometallic Catalysis Edited by Cornils, Boy; Herrmann, Wolfgang A (1998), 577-581. 29. Joo, Ferenc; Katho, Agnes Aqueous-Phase Organometallic Catalysis Edited by Cornils, Boy; Herrmann, Wolfgang A (1998), 340-371. 30. Fontal B, Anzelotti A, Reyes M, et al. CATAL LETT 59 (1999) 187-190. 31. Jiang H, Xu Y, Liao SJ, et al. J MOL CATAL A-CHEM 142 (1999) 147-152. 32. Timokhin BV, Baransky VA, Eliseeva GD USP KHIM 68 (1999) 80-93. 33. Elliott, Douglas C.; Frye, John G. U.S. (1999), US 5883266 A 19990316. 34. Bozell JJ, Moens L, Elliott DC, et al. RESOUR CONSERV RECY 28 (2000) 227-239. 35. Kovacs G, Nadasdi L, Joo F, et al., CR ACAD SCI II C 3 (2000) 601-605. 36. Bergbreiter, David E. ACS Symposium Series (2000), 767(Green Chemical Syntheses and Processes), 182-193. 37. Crooks, Richard M.; Lemon, Buford I., III; Sun, Li; Yeung, Lee K.; Zhao, Mingqi Topics in Current Chemistry (2001), 212 (Dendrimers III), 81-135. 38. Joó F., ACCOUNTS OF CHEMICAL RESEARCH, 35 (2002) 738-745. 39. Vancheesan, S.; Jesudurai, D. Catalysis: Principles and Applications, [Orientation Programme], Indian Institute of Technology, Dep. of Chemistry, Madras, India, Edited by Viswanathan, B.; Sivasanker, S.; Ramaswamy, A. V 2000 (2002) 311-337. 40. Cornils, Boy; Herrmann, Wolfgang A. Applied Homogeneous Catalysis with Organometallic Compounds (2nd Edition) Edited by Cornils, Boy; Herrmann, Wolfgang A (2002), 2, 603-633. 41. Crooks, Richard M.; Chechik, Victor; Lemon, Buford I., III; Sun, Li; Yeung, Lee K.; Zhao, Mingqi Metal Nanoparticles Edited by Feldheim, Daniel L.; Foss, Colby A., Jr (2002), 261-296. 42. Joo, Ferenc; Katho, Agnes Aqueous-Phase Organometallic Catalysis (2nd Edition) Edited by Cornils, Boy; Herrmann, Wolfgang A (2004), 429-463. 43. Pettinari, C.; Marchetti, F.; Martini, D. Comprehensive Coordination Chemistry II Edited by McCleverty, Jon A.; Meyer, Thomas J (2004), 9, 75-139. 44. Jiang, Nan; Li, Chao-Jun Environmental Catalysis Edited by Grassian, Vicki H (2005), 91-608. 45. Delhomme C, Weuster-Botz D, Kuhn FE, GREEN CHEMISTRY 11 (2009) 13-26. 46. Shaughnessy KH, CHEMICAL REVIEWS 109 (2009) 643-710. 47. Yan ZP, Lin L, Liu SJ, ENERGY & FUELS 23 (2009) 3853-3858. 48. Akien, Geoffrey; Qi, Long; Horvath, Istvan T. RSC Energy and Environment Series (2010), 1(Thermochemical Conversion of Biomass to Liquid Fuels and Chemicals), 365-381. 49. Gong Y, Lin L, Yan ZP, BIORESOURCES 6 (2011) 686-699. 10. I. F. Szabó, L. Somsák, I. Farkas: C-Nucleosides V. Synthesis of 5-(D-Glycosyl)-2-halogenomethyl- and -2-azidomethyl-1,3,4- oxadiazoles Acta Chim. Acad. Sci. Hung., 115 (1984) 319-325. IF: 0.477 (1984) Cited by/Idézi: 1. H. Hrebabecky, Coll. Czech. Chem. Commun., 51 (1986) 1311-1315. 2. L. Somsák, Gy. Batta, I. Farkas, Carbohydr. Res., 124 (1983) 43-51. 3. L. Somsák, R. J. Ferrier, Adv. Carbohydr. Chem. Biochem., 49 (1991) 37-92. 4. I. Farkas, K. Peseke, H. Kristen, Wiss. Z. WPU Rostock, Naturwiss. Reihe, 32 (1983) 1-64 6
5. S. H. Mahmoud, L. Somsák, I. Farkas, Carbohydr. Res., 254 (1994) 91-104. 6. Houben-Weyl, E8c, p. 591. 7. N. R. Williams, B. E. Davison, R. J. Ferrier, R. H. Furneaux, R. H. Wightman, Carbohydr. Chem., Vol. 18., Royal Soc. Chem., London, 1986, p. 200. 8. M. A. E. Shaban, A. Y. Nasr, Adv. Heterocycl. Chem., 68 (1997) 225-432. 9. KNUTSEN LJS, NUCLEOSIDES & NUCLEOTIDES, 11 (5): 961-983 1992. 10. Lipták A., Pintér I., Somsák L., Magy. Kém. Folyóirat, 108 (2002) 467-491. 11. L. Somsák, Gy. Batta, I. Farkas: Preparation of Acetylated Hepto- and Hexopyranos-2-ulononitriles from Acetylated 1- Bromo-D-glycosyl Cyanides Carbohydr. Res., 132 (1984) 342-344. IF: 1.341 (1984) Cited by/Idézi: 1. I. Farkas, G. Snatzke, L. Somsák, Liebigs Ann. Chem., (1989) 599-600. 2. L. Párkányi, A. Kálmán, L. Somsák, I. Farkas, Carbohydr. Res., 168 (1987) 1-5. 3. L. Somsák, Gy. Batta, I. Farkas, L. Párkányi, A. Kálmán, Á. Somogyi, J. Chem. Res., S (1986) 436-437; M 3543-3566. 4. L. Somsák, E. Papp, Gy. Batta, I. Farkas, Carbohydr. Res., 211 (1991) 173-178. 5. J. G. Buchanan, A. P. W. Clelland, T. Johnson, R. A. C. Rennie, R. H. Wightman, J. Chem. Soc., Perkin Trans. I, (1992) 2593-2601. 6. L. Somsák, R. J. Ferrier, Adv. Carbohydr. Chem. Biochem., 49 (1991) 37-92. 7. P. M. Harrington, M. E. Jung, Tetrahedron Lett., 35 (1994) 5145-5148. 8. J.-P. Praly, C. Di Stefano, G. Descotes, R. Faure, L. Somsák, I. Eperjesi, Tetrahedron Lett., 36 (1995) 3329- 3332. 9. L. Somsák, E. Sós, Z. Györgydeák, J.-P. Praly, G. Descotes, Tetrahedron, 52 (1996) 9121-9136. 10. N. R. Williams, B. E. Davison, R. J. Ferrier, R. H. Furneaux, R. H. Wightman, Carbohydr. Chem., Vol. 18., Royal Soc. Chem., London, 1986, p. 110. 11. J.-P. Praly, C. Di Stéfano, L. Somsák, M. Hollósi, Zs. Majer, W. Voelter, Tetrahedron: Asymmetry, 10 (1999) 901-911. 12. L. Somsák, Gy. Batta, I. Farkas, L. Párkányi, A. Kálmán, Á. Somogyi: Synthesis and Stereochemistry of a New Spiro Glycosylidene Heterocycle from the Reaction of 1-Bromoglycosyl Cyanides with S-Nucleophiles: Complete Identification of Hydrogen Bridges by N.M.R. Methods and X-ray Analysis J. Chem. Res., S (1986) 436-437; M (1986) 3543-3566. IF: 0.637 (1986) Cited by/Idézi: 1. L. Somsák, E. Papp, Gy. Batta, I. Farkas, Carbohydr. Res., 211 (1991) 173-178. 2. L. Somsák, R. J. Ferrier, Adv. Carbohydr. Chem. Biochem., 49 (1991) 37-92. 3. J.-P. Praly, C. Di Stefano, G. Descotes, R. Faure, L. Somsák, I. Eperjesi, Tetrahedron Lett., 36 (1995) 3329- 3332. 4. L. Somsák, E. Sós, Z. Györgydeák, J.-P. Praly, G. Descotes, Tetrahedron, 52 (1996) 9121-9136. 5. N. R. Williams, B. E. Davison, R. J. Ferrier, R. H. Furneaux, P. C. Tyler, R. H. Wightman, Carbohydr. Chem., Vol. 21., Royal Soc. Chem., London, 1989, p. 113. 6. E. Ősz, L. Szilágyi, L. Somsák, A. Bényei, Tetrahedron, 55 (1999) 2419-2430. 7. W. Wenger, A. Vasella, Helv. Chim. Acta, 83 (2000) 1542-1560. 8. Lipták A., Pintér I., Somsák L., Magy. Kém. Folyóirat, 108 (2002) 467-491. 7
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- Page 17 and 18: 41. Capozzi, Giuseppe; Menichetti,
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- Page 33 and 34: 16. Marinov M, Minchev S, Stoyanov
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synthesis and enzymatic evaluation
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27. Benltifa, M., De Kiss, M., Isab
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31. Somsák L., Bokor É., Czifrák
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79. K. Czifrák, Zs. Hadady, T. Doc
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Cited by/Idézi: 1. L. Somsák, V.
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85. L. Somsák, K. Czifrák, M. Tó
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12. Shahid I. Awan, Daniel B. Werz,
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Bioorg. Med. Chem., 17 (2009) 4773-
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IF: 1.898 (2010) Cited by/Idézi: 1
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106. M. Tóth, S. Kun, L. Somsák,
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B) ÉRTEKEZÉSEK 1. Vízoldható r
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D) MŰBÍRÁLATOK 1. Report on the