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Tytuł artykułu

Glikozylacja z zastosowaniem pochodnych 1-tiocukrów jako substratów

Identyfikatory
Warianty tytułu
EN
Derivatives of 1-thiosugars as substrates in glycosylation reactions
Języki publikacji
PL
Abstrakty
EN
It was found that carbohydrate part of complex glycosides may act as antigens or receptors for proteins, and these findings led to the discovery of the important role of carbohydrates in cell-cell recognition phenomena and cell differentiation. At the same time the methods of glycosylation underwent rapid development. The present paper gives an overview of development of 1-thiosugar derivatives in oligosaccharide synthesis. In the first part of this review, recent results of the use of thioglycosides, dithiocarbonates, dithiocarbamates and thiophosphates as glycosyl donors and acceptors are presented. A survey of important methods for the synthesis of thiosugars is presented, followed by discussion of methods converting anomeric substituent into a good leaving group (activation) in nucleophilic substitution reaction. The mechanism and procedures, which provide stereoselective formation of 1,2-cis and 1,2-trans glycoside bond, are discussed. The versatility of 1-thiosugar derivatives in synthetic carbohydrate chemistry is illustrated by selective activation strategies. The most important synthetic methodologies of the synthesis of oligosaccharides like linear glycosylation strategy in step-by-step and multistep "one-pot" sequence, "armed-disarmed" glycosyl donor, "latent-active" glycosylation, orthogonal strategy are illustrated on several examples. The last part is devoted to methods for solid support oligosaccharide synthesis.
Rocznik
Strony
605--625
Opis fizyczny
schem., bibliogr. 73 poz.
Twórcy
autor
autor
autor
autor
autor
autor
autor
autor
  • Wydział Chemiczny, Politechnika Śląska ul. B.Krzywoustego 8, 44-100 Gliwice
Bibliografia
  • [1] H. Lis, N. Sharon, Eur. J. Biochem., 1993, 218, 1.
  • [2] A. Varki, Glycobiology, 1993, 3, 97.
  • [3] P. Sears, C.-H Wong, Cell. Mol. Life Sci., 1998, 54, 223.
  • [4] P. Roussel, G. Lamblin, [w:] Glycoproteins and Diseases, J. Montreuil, J.F.G. Vliegenthart, H. Schacter (red.), Elsevier. Amsterdam 1966, 351-493.
  • [5] R.C. Hughes, Membrane Glycoproteins, Butterworths, London 1976.
  • [6] J. Montreuil, Adv. Carbohydr. Chem. Biochem., 1980, 37, 157.
  • [7] P. Sears, C.-H. Wong, Angew. Chem. Int. Ed. Engl., 1999, 38, 2300.
  • [8] P.J. Garegg, Adv. Carbohydr. Chem. Biochem., 1997, 52, 179.
  • [9] H. Paulsen, Angew. Chem. Int. Ed. Engl., 1990, 29, 823.
  • [10] R. R. Schmidt, YV. Kinzy, Adv. Carbohydr. Chem. Biochem., 1994. 50, 21.
  • [11] S. Danishefsky, M.T. Bilodeau. Angew. Chem. Int. Ed. Engl., 1996, 35, 1380.
  • [12] S. Hannessian, Preparative Carbohydrate Chemistry, Marcel Dekker, New York 1997.
  • [13] G.-J. Boons, Tetrahedron, 1996, 52, 1095.
  • [14] K. Toshima, K. Tatsuta, Chem. Rev., 1993, 93, 1503.
  • [15] S.H. Khan, R.A. O’Neill, Modern Methods in Carbohydrate Synthesis, Harwood Academic Publishers, 1996.
  • [16] H. Driguez, J. Thiem, Glycoscience, Springer Verlag, Berlin 1999.
  • [17] R.G. Pearson. J. Am. Chem. Soc.. 1963, 85, 3533; Science, 1966. 151, 172.
  • [18] R.J. Ferrier, R.W. Hay, N. Vethaviyaser, Carbohydr. Res., 1973, 27, 545.
  • [19] H. Lönn, Carbohydr. Res., 1985, 139, 115.
  • [20] P. Fügedi, P.J. Garegg, Carbohydr. Res., 1986, 149, C9.
  • [21] V. Pozsgay, H.J. Jennings, J. Org. Chem., 1987, 52, 4635.
  • [22] Y. Ito, T. Ogawa, Tetrahedron Lett., 1988, 29, 1061.
  • [23] F. Dasgupta, P.J. Garegg, Carbohydr. Res., 1988, 177, C l3.
  • [24] G.H.Veeneman. S.H. Van Leeuwen, J.H. Van Boom, Tetrahedron Lett., 1990, 31, 1331.
  • [25] H.M. Zuurmond, G.A. van der Marel, J.H. van Boom, Reel. Trav. Pays-Bas, 1993, 112, 507.
  • [26] S.H. Kim, D. Augeri, D. Yang, D. Kahne, J. Am. Chem. Soc., 1994,116, 1766.
  • [27] E. Fischer, K. Delbrück, Chem. Ber., 1909, 42, 1476.
  • [28] J. Bogusiak, W. Szeja, Polish J. Chem., 1985, 59, 293.
  • [29] M. Apparu, M. Blanc-Muesser, J. Defaye, H. Driguez, Can. J. Chem., 1981, 59, 314.
  • [30] T. Norberg, [w:] Modern Methods in Carbohydrate Synthesis, S.H. Khan, R.A. O’Neill (red.), Harwood Academic Publishers, 1996, 86 i literature cytowana.
  • [31] H. Driguez, W. Szeja, Synthesis, 1994, 1413.
  • [32] a) G. Pastuch, W. Szeja, Carbohydr. Lett., 1997, 2,281; b) B. Przybysz, W. Szeja, K. Walczak, J. Suwinski, Polish. J. Chem., 1997, 71, 1421.
  • [33] M. Cemy, J. Pacak, Chem. Listy 1958, 52, 2090.
  • [34] I. Fokt, W. Szeja, Carbohydr. Res., 1992, 232, 169.
  • [35] I. Fokt. J. Bogusiak, W. Szeja, Carbohydrate Letters 1998, 3, 191.
  • [36] S. Tejima, S. Ishiguro, Chem. Pharm. Bull., 1967, 15, 255.
  • [37] P. Fügedi, J. Garegg, S. Oscarson, Carbohydr. Res., 1991, 211, 157.
  • [38] A. Marra, P. Sinay, Carbohydr. Res., 1989,187, 35.
  • [39] W. Szeja, J. Bogusiak, Synthesis, 1988, 224.
  • [40] W. Szeja, J. Bogusiak, Carbohydr. Res., 1987,170, 235.
  • [41] J. Bogusiak, I. Wandzik, W. Szeja, Carbohydr. Lett., 1996,1, 411.
  • [42] I. Wandzik, W. Szeja, Polish J. Chem., 1998, 72, 703.
  • [43] J. Bogusiak, W. Szeja, Carbohydr. Res., 1996, 295, 235.
  • [44] I, Wandzik, W. Szeja, Polish J. Chem., 1999, 73, 1163.
  • [45] A. Marra, F. Gauffeny, P. Sinay, Tetrahedron, 1991, 47, 5149.
  • [46] M. Michalska, J. Michalski, I. Orlich, Tetrahedron, 1978, 34, 617.
  • [47] S. Hashimoto. T. Honda. S. Ikegami. Tetrahedron Lett., 1990, 31, 4769.
  • [48] T. Inazu, H. Hosokawa. Y. Satoh, Chem. Lett.. 1985, 297.
  • [49] a) T. Inazu, T. Yamanoi, Chem. Lett., 1989, 69; c) T. Yamanoi, T. Inazu, Chem. Lett., 1990, 849.
  • [50] J. Bogusiak, Polish J. Chem., 1999, 73, 619.
  • [51] a) J. Bogusiak, W. Szeja, Synlett., 1997, 6, 661; b) J. Bogusiak, W. Szeja, Carbohydr. Res., 2001, 330, 141.
  • [52] M. Chmielewski. J.N. BeMiller. Carbohydr. Res., 1981, 96. 73.
  • [53] J. Bogusiak, W. Szeja. J. Carbohydr. Chem.. 1991. 10. 47.
  • [54] J Borowiecka, P. Lipka, M. Michalska, Tetrahedron, 1988, 44, 2067.
  • [55] M. Michalska, J. Borowiecka, J. Carbohydr. Chem., 1983, 2, 99.
  • [56] L. Laupichler, H. Sajus, J. Thiem, Synthesis. 1992, 1133.
  • [57] H. Bielawska, M. Michalska, J. Carbohydr. Chem., 1991,10, 107.
  • [58] a) F. Barresi, O. Hindsgaul, J. Am. Chem. Soc., 1991,113, 9376; b) F. Barresi, O. Hindsgaul, Can. J. Chem., 1994. 72. 1447.
  • [59] G. Stork, G. Kim, J. Am. Chem. Soc., 1992,114, 1087.
  • [60] P. Sinay, J.-M. Mallet, [w:] Modern Methods in Carbohydrate Synthesis, S.H. Khan, R.A. O’Neill (red.), Harwood Academic Publishers, 1996, 130 i literatura cytowana.
  • [61] A. Marra, J.-M. Mallet, C. Amatore, P. Smas, Synlett., 1990, 572.
  • [62] D. Kahne, S. Walker, Y. Cheng, D. Van Engen, J. Am. Chem. Soc., 1989, 111. 6881; S. Raghavan, D. Kahne, J. Am. Chem. Soc., 1993,115, 1580,
  • [63] a) Z. Zhang, I.R. Ollmann. X.-S. Ye. R. Wischant, T. Baasov. C-H. Wong, J. Am. Chem. Soc. 1999,121, 734; b) P. Sears, C.-H. Wong, Science, 2001, 291, 2344.
  • [64] a) G.H. Veeneman, S.H. van Leeuwen, J.H. van Boom, Tetrahedron Lett., 1990, 31 1331; b) G.H. Veeneman, J.H. van Boom, Tetrahedron Lett., 1990, 31, 275.
  • [65] P. Konradson, U.E. Udodong, B. Fraiser-Reid, Tetrahedron Lett., 1990, 31, 4313.
  • [66] G.J. Boons, P. Geurtsen, D. Holmes, Tetrahedron Lett., 1995, 34, 6325.
  • [67] R. Roy, F.O. Andersson, M. Letellier, Tetrahedron Lett, 1992, 33, 6053.
  • [68] G. Pastuch, I. Wandzik, W. Szeja, Tetrahedron Lett., 2000, 41, 9923.
  • [69] J. Bogusiak, W. Szeja, Tetrahedron Lett., 2001, 42, 2221.
  • [70] O. Kanie, Y. Ito, T. Ogawa, J. Am. Chem. Soc., 1994,116, 12073.
  • [71] J.J. Krepinsky, [w:] Modem Methods in Carbohydrate Synthesis, S.H. Khan, R.A. O’Neill (red.), Harwood Academic Publishers, 1996, 194 i literatura cytowana.
  • [72] S.P. Douglas, D.M. Whitfield, J.J. Krepinsky, J. Am. Chem. Soc., 1991,113, 5095.
  • [73] R. Verduyn, P.A.M van der Klein, M. Douwes, G.A. van der Marel, J.H. van Boom, Reel. Trav. Chim. Pays-Bas, 1993,112, 464.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-article-BUS1-0010-0076
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