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Катализируемый краун-соединениями синтез в-арилгликозидов N-ацетилглюкозамина / В. О. Курьянов, Т. А. Чупахина, А. Е. Земляков, С. А. Котляр, Г. Л. Камалов, В. Я. Чирва // Биоорганическая химия. — 2001. — Т. 27, № 6. — С. 434−438. Crich D., Sun S. Direct formation of в-mannopyranosides from thioglycosides / D. Crich, S. Sun // J. Am. Chem. Soc. -1998. — Vol. 120. — P. 435−436. (b) Crich D., Sun… Читать ещё >

Список цитируемой литературы (реферат, курсовая, диплом, контрольная)

1. Бочков А. Ф. Углеводы / А. Ф. Бочков, В. А. Афанасьев, Г. Е. Заиков — М.: Наука, 1980, 176 с.

2. Бочков А. Ф. Образование и расщепление гликозидных связей / В. А. Афанасьев, Г. Е. Зайков — М.: Наука, 1978. 180 с.

3. Magnusson G. Synthesis of 3?- and 4?-deoxyfluorolactose and its Me3SiCH2CH2 and ceramide derivatives / G. Magnusson // Trends Glycosci. Glycotechnol- 1992. — Vol. 4. — P. 358−367.

4. 2-(Trimethylsilyl)ethyl glycosides. 3. Synthesis, anomeric deblocking, and transformation into 1,2-trans 1-O-acyl sugars / K. Jansson, S. Ahlfors, T. Frejd, J. Kihlberg, G. Magnusson, G. Noori, K. Stenvall [et al.] // J. Org. Chem. — 1988. — Vol. 53. — P. 5629−5647.

5. 2-(Trimethylsilyl)ethyl glycosides. Transformation into glycopyranosyl chlorides / K. Jansson, G. Noori, G. Magnusson [et al.] // J. Org. Chem. — 1990. — Vol. 55. — P. 3181−3185.

6. Kartha K.P.R., Jennings H.J. A facile, one-step procedure for the conversion of 2-(trimethylsilyl)ethyl glycosides to their glycosyl chlorides / K.P.R. Kartha, H.J. Jennings // Tetrahedron Lett. — 1990. — Vol. 31. — P. 2537−2540.

7. Племенков В. В.

Введение

в химию природных соединений. / В. В. Племенков — Казань, 2001, 376 с.

8. Fischer E. Ьber die Glucoside der Alkohole / E. Fischer // Ber. — 1893. — Vol. 26. — P. 2400−2412.

9. Bishop C. T., Cooper F. P. Glycosidation of sugars. II. Methanolysis of D-xylose, D-lyxose, and D-ribose / C. T. Bishop, F. P. Cooper // Can. J. Chem. — 1963. — Vol. 41. — P. 2743−2758.

10. Lindberg B. Action of strong acids on acetylated glycosides. V. Synthesis of в-isomaltose octaacetate / B. Lindberg // Acta Chem. Scand. — 1949. — Vol. 3. — P. 1355−1357.

11. Kiso M. Protected Glycosides and Dysaccharides of 2-amino-2-deoxy-D-glucopyranose by ferric chloride-catalyzed coupling / M. Kiso, L. Anderson // Carb. Res. — 1985. — P. 315−316.

12. Helferich B., Wedemeyer K. F. Preparation of glucosides from acetobromoglucose / B. Helferich, K. F. Wedemeyer // Ann. — 1949. — Vol. 563. — P. 139−145.

13. Helferich B., Weis K. The synthesis of glucosides and of nonreducing disaccharides / B. Helferich, K. Weis // Chem. Ber. — 1956. — Vol. 89. — P. 314−321.

14. Helferich B., Zirner J. Synthesis of tetra-O-acetylhexoses with a free 2-hydroxyl group. Synthesis of disaccharides / B. Helferich, J. Zirner // Chem. Ber. — 1962. — Vol. 95. — P. 2604−2611.

15. Lemieux R. U., Suemitsu R., Gunner G. S. W. Stereoselective synthesis of б-D-glucopyranosides / R. U. Lemieux, R. Suemitsu, G. S. W. Gunner // Can. J. Chem. — 1968. — Vol. 46. — P. 1040−1041.

16. Reaction of dimeric tri-O-acetyl-2-deoxy-2-nitroso-б-hexopyranosyl chlorides with alcohols / R. U. Lemieux, Y. Ito, K. James, T. L. Nagabhushan [et al.] // Can. J. Chem. — 1973. — Vol. 51. — P. 7−18.

17. Reduction of isopropyl tri-O-acetyl-2-oximino-б-D-hexopyranosides / R. U. Lemieux, Y. Ito, K. James, T. L. Nagabhushan [et al.] // Can. J. Chem. — 1973. -Vol. 51. — P. 33−41.

18. Lemieux R. U., James K., Nagabhushan T. L. Chemical syntheses of б-linked disaccharides / R. U. Lemieux, K. James, T. L. Nagabhushan // Can. J. Chem. — 1973. — Vol. 51. — P. 42−47.

19. Lemieux R. U., James K., Nagabhushan T. L. Chemical synthesis of б-linked 2'-amino-2'-deoxydisaccharides / R. U. Lemieux, K. James, T. L. Nagabhushan // Can. J. Chem. — 1973. — Vol. 51. — P. 48−52.

20. Synthesis of derivatives of N-acetyl-D-lactosamine from D-lactal hexaacetate. Hexa-O-acetyl-2-deoxy-2-phthalimido-в-D-lactosyl chloride / R. U. Lemieux, S. Z. Abbas, M. H. Burzynska, R. M. Ratcliffe // Can. J. Chem. — 1982. -Vol. 60. — P. 63−67.

21. Lemieux R. U., Ratcliffe R. M. The azidonitration of tri-O-acetyl-D-galactal / R. U. Lemieux, R. M. Ratcliffe // Can. J. Chem. — 1979. — Vol. 57. — P. 1244−1251.

22. Halide ion catalyzed glycosidation reactions. Syntheses of б-linked disaccharides / R. U. Lemieux, K. B. Hendricks, R. V. Stick, K. James // J. Am. Chem. Soc. — 1975. — Vol. 97. — P. 4056−4062.

23. Lemieux R. U., Driguez H., J. Am. Chem. Soc. — 1975. — Vol. 97. — P. 4069.

24. A mechanistic study the nucleophilic dependence in glucosylations with glucosyl bromides / T. Bowden, P. J. Garegg, P. Konradsson, J. L. Maloisel // Israel J. Chem. — 2001. — Vol. 40. — P. 271−277.

25. Charnaciтn M., Chacтn-Fuertes M. E., Martin-Lomas M. Chemical syntheses of 4-O-бand в-D-galactopyranosyl-D-galactose and 3-O-б andв-D-galactopyranosyl-D-galactose / M. Charnaciтn, M. E. Chacтn-Fuertes, M. Martin-Lomas // Carbohydr. Res. — 1975. — Vol. 43. — P. 51−56.

26. Lemieux R. U. Haworth Memorial Lecture. Human blood groups and carbohydrate chemistry / R. U. Lemieux // Chem. Soc. Revs. — 1978. — Vol. 7. — P. 423−452.

27. Paulsen H., Lockhoff O. Building blocks for oligosaccharides. XV. Synthesis of в-D-mannopyranosyland 2-azido-2-deoxy-б-D-glucopyranosyl-containing disaccharide halide building blocks / H. Paulsen, O. Lockhoff // Tetrahedron. Lett. — 1978. — P. 4027−4030.

28. Paulsen H., Stenzel W. Building units for oligosaccharides, IX. Stereoselective synthesis of б-glycosidically linked diand oligosaccharides of 2-amino-2-deoxy-D-glucopyranose / H. Paulsen, W. Stenzel // Chem. Ber. — 1978. — Vol. 111. — P. 2234−2347.

29. Paulsen H., Stenzel W. Building units for oligosaccharides, X. Synthesis of б-1>4 and б-1>3 linked disaccharides of 2-amino-2-deoxy-D-glucopyranose by the azide method / H. Paulsen, W. Stenzel // Chem. Ber. — 1978. — Vol. 111. — P. 2348−2357.

30. Paulsen H., Kolar C. Building units for oligosaccharides. XVI. Synthesis of the oligosaccharide determinants of the blood-group substances of type 1 of the ABH system / H. Paulsen, C. Kolar // Chem. Ber. — 1979. — Vol. 112. — P. 3190−3202.

31. A novel glucosidation reaction. Application to the synthesis of бlinked disaccharides / J. R. Pougny, M. A. M. Nassr, N. Naulet, P. Sinaя [et al.] // Nouv. J. Chim. — 1978. — Vol. 2. — P. 389−395.

32. Sinaя P. Recent advances in glycosylation reactions / P. Sinaя // Pure Appl. Chem. — 1978. — Vol. 50. — P. 1437−1452.

33. Schmidt R. R., Michel J. Simple syntheses of бand в-O-glycosyl imidates; preparation of glycosides and disaccharides / R. R. Schmidt, J. Michel // Angew. Chem. Int. Edn. Engl. — 1980. — Vol. 19. — P. 731−732.

34. Schmidt R. R., Grundler G. б-Linked disaccharides from O-(в-D-glucopyranosyl)-trichloroacetimidates using trimethylsilyltrifluoromethan-esulfonate as catalyst / R. R. Schmidt, G. Grundler // Angew. Chem.Suppl. — 1982. — Vol. 2. — P. 1707−1715.

35. Еkerfeldt K., Garegg P. J., Iversen T. Facile synthes is of aryl в-D-mannopyranosides / K. Еkerfeldt, P. J. Garegg, T. Iversen // Acta Chem. Scand., — 1979. — Vol. B33. — P. 467−468.

36. G. Ekborg, B. Lindberg, Lцnngren J. Synthesis of в-D-mannopyranosides / Ekborg G., Lindberg B., J. Lцnngren // Acta Chem. Scand. — 1972. — Vol. 26. — P. 3192−3287.

37. Benzylated orthoesters in glycoside synthesis. The synthesis of б-D-glucopyranosides and в-D-mannopyranosides / H.B. Borйn, G. Ekborg, K. Eklind, P.J. Garegg, ?. Pilotti, C.-G. Swahn [et al.] // Acta Chem. Scand. — 1973. — Vol. 27. — P. 2639−2644.

38. Garegg P.J., Samuelsson B. Oxidation of primary and secondary alcohols in partially protected sugars with the chromium trioxide-pyridine complex in the presence of acetic anhydride / P.J. Garegg, B. Samuelsson // Carbohydr. Res. — 1978. — Vol. 67. — P. 267−270.

39. Enantiopure building blocks from sugars. 14. Various glycosyl donors with a ketone or oxime function next to the anomeric center: facile preparation and evaluation of their selectivities in glycosidations / Lichtenthaler F. W., Klaeres U., Lergenmueller M., Schwidetzky S. [et al.] // Synthesis. -1992. — P. 179−184.

40. Kaji E., Lichtenthaler F. W. 2-Oxoand 2-oximinoglycosyl halides: versatile glycosyl donors for the construction of в-D-mannose and в-D-mannosamine-containing oligosaccharides / E. Kaji, F. W. Lichtenthaler // Trends Glycosci. Glycotech. — 1993. — Vol. 5. — P. 121−142.

41. Paulsen H., Lockhoff O. Building units for oligosaccharides. XXX. New effective в-glycoside synthesis of mannose glycosides. Syntheses of mannose containing oligosaccharides / H. Paulsen, O. Lockhoff // Chem. Ber. — 1981. — Vol. 114. — P. 3102−3114.

42. Garegg P. J., Ossowski P. Silver zeolite as promoter in glycoside synthesis. The synthesis of в-D-mannopyranosides / P. J. Garegg, P. Ossowski // Act. Chem. Scand. — 1983. — Vol. 37. — P. 249−250.

43. Gorin P. A. J., Perlin A. S. Configuration of glycosidic linkages in oligosaccharides. IX. Synthesis of бand в-D-mannopyranosyl disaccharides / P. A. J. Gorin, A. S. Perlin // Can. J. Chem. — 1961. — Vol. 39. — P. 2474−2485.

44. Bebault G.M., Dutton G.G.S. Synthesis of 4-O-в-D-mannopyranosyl-L-rhamnopyranose / G.M. Bebault, G.G.S. Dutton // Carbohydr. Res. — 1974. — Vol. 37. — P. 309−319.

45. Synthesis of the pentasaccharide repeating unit of the O-specific polysaccharide from Salmonella strasbourg / N.K. Kochetkov, V. L. Torgov, N.N. Malysheva, A.S. Shashkov [et al.] // Tetrahedron. — 1980. — Vol. 36. — P. 1099−1105.

46. Practical synthesis of O-в-Dmannopyranosyl-, O-б-D-mannopyranosyland O-в-D-glucopyranosyl-(1>4)-O-б-L-rhamnopyranosyl-(1>3)-D-galacto-es / V. I. Betaneli, M. V. Ovchinnikov, L. V. Backinowsky, N. K. Kochetkov [et al.] // Carbohydr. Res. — 1980. — Vol. 84. — P. 211−214.

47. Wulff G., Wichelhaus J. Studies on glycoside synthesis. IX. Synthesis of в-D-mannopyranosides / G. Wulff, J. Wichelhaus // Chem. Ber. — 1979. — Vol. 112. — P. 2847−2853.

48. Garegg P.J., Iversen T., Johansson R. Synthesis of disaccharides containing в-D-mannopyranosyl groups / P.J. Garegg, T. Iversen, R. Johansson // Acta Chem. Scand. — 1980. — Vol. 34. — P. 505−508.

49. (a) Crich D., Sun S. Direct formation of в-mannopyranosides from thioglycosides / D. Crich, S. Sun // J. Am. Chem. Soc. -1998. — Vol. 120. — P. 435−436. (b) Crich D., Sun S. Formation of вmannopyranosides of primary alcohols using the sulfoxide method / D. Crich, S. Sun // J. Org. Chem. -1996. — Vol. 61. — P. 4506−4507.

50. Crich D., Sun S. Direct synthesis of в-mannopyranosides by the sulfoxide method / D. Crich, S. Sun // J. Org. Chem. -1997. — Vol. 62. — P. 1198−1199.

51. Barresi F., Hindsgaul O. Synthesis of в-mannopyranosides by intramolecular aglycon delivery / F. Barresi, O. Hindsgaul // J. Am. Chem. Soc. -1991. — Vol. 113. — P. 9376−9377.

52. Tebbe F. N., Parshall G. W., Reddy G. S. Olefin homologation with titanium methylene compounds / F. N. Tebbe, G. W. Parshall, G. S. Reddy // J. Am. Chem. Soc. -1978. — Vol. 100. — P. 3611−3613.

53. Stork G., Kim G., Stereocontrolled synthesis of disaccharides via the temporary silicon connection / G. Stork, G. Kim // J. Am. Chem. Soc. -1992. — Vol. 114. — P. 1087−1088.

54. Ito Y., Ogawa T. A new approach to stereoselective synthesis of в-mannosides/ Y. Ito, T. Ogawa // Angew. Chem. Int. Ed. Eng. -1994. — Vol. 33. — P. 1765−1767.

55. Kochetkov N. K., Bochkov A. F. Synthesis of oligosaccharides by the orthoester method / N. K. Kochetkov, A. F. Bochkov // Methods Carbohydr. Chem. -1972. — Vol. 6. — P. 480−486.

56. Garegg P. J., Lindberg B., Samuelsson B. Synthesis of 1-O-в-D-ribofuranosyl-D-ribitol / P. J. Garegg, B. Lindberg, B. Samuelsson // Carbohydr. Res. -1977. — Vol. 58. — P. 219−221.

57. Gallo-Rodriguez C., Varela O., de Lederkremer R. M. First synthesis of в-D-Galf (1>4) GlcNAc, a structural unit attached O-glycosidically in glycoproteins of Trypanosomacruzi / C. Gallo-Rodriguez, O. Varela, R. M. de Lederkremer // J. Org. Chem. -1996. — Vol. 61. — P. 1886−1889.

58. Synthesis of the Leishmania LPG core heptasaccharyl myo-inositol / K. Ruda, J. Lindberg, P. J. Garegg, S. Oscarson, P. Konradsson [et al.] // J. Am. Chem. Soc. — 2000. — Vol. 122. — P. 11 067−11 072.

59. Jacquinet J.-C., Zurabyan S. E., Khorlin A. A. Oxazoline synthesis of 1,2-trans-2-acetamido-2-deoxyglycosides. Glycosylation with methyl-(3,4,6-tri-O-acetyl-1,2-dideoxy-б-D-galactopyrano)-[2', 1':4,5]-2-oxazoline / J.-C. Jac-quinet, S. E. Zurabyan, A. A. Khorlin // Carbohydr. Res. — 1974. — Vol. 32. — P. 137−143.

60. Hanessian S., Banoub J. Innovations in synthetic carbohydrate chemistry—practical and conceptual approaches to glycoside synthesis / S. Hanessian, J. Banoub // Am. Chem. Soc. Symp. Ser. — 1976. — Vol. 39. — P. 36−63.

61. Hanessian S., Banoub J. Chemistry of the glycosidic linkage. An efficient synthesis of 1,2-trans-disaccharides / S. Hanessian, J. Banoub // Carbohydr. Res. — 1977. — Vol. 53. — P. 13 — 16.

62. Lemieux R. U., Takeda T., Chung B.Y. Synthesis of 2-amino-2-deoxy-в-D-glucopyranosides. Properties and use of 2-deoxy-2-phthalimidoglycosyl halides / R. U. Lemieux, T. Takeda, B.Y. Chung // Am. Chem. Soc Symp. Ser. — 1976. — Vol. 39. — P. 90−115.

63. Legermьller M., Ito Y., Ogawa T. Use of Dichloropthaloyl (DCPhth) group as amino protection group in oligosaccharide synthesis / M. Legermьller, Y. Ito, T. Ogawa // Tetrahedron. — 1998. — Vol. 54. — P. 1381−1394.

64. Two neworthogonal amine-protecting groups that can be cleaved under mild or neutral conditions/ J. S. Debenham, R. Madsen, C. Roberts, B. Fraser-Reid [et al.] // Am. Chem. Soc. — 1995. — Vol. 117. — P. 3302−3303.

65. Castro-Papermo J. C., Schmidt R. R. Glycoslimidates. 72. N-Tetrachlorophthaloyl-protected trichloroacetimidate of glucosamine as glycosyl donor in oligosaccharide synthesis / J. C. Castro-Papermo, R. R. Schmidt // Tetrahedron Lett. — 1995. — Vol. 36. — P. 5343−5346.

66. Garegg P. J., Norberg T. Observations on silver trifluoromethane sulfonate-promoted syntheses of 1,2-trans-glycosides from acylated glycosyl bromides / P. J. Garegg, T. Norberg // Acta Chem. Scand. — 1979. — Vol. 33. — P. 116−118.

67. Райхард К. Растворители и эффекты среды в органической химии / K. Райнхард. — Пер. с англ. / Под ред. Петросяна В. С. — М.: Мир, 1991. — 763 с.

68. Беспамятнов Г. П. Предельно допустимые концентрации химических веществ в окружающей среде / Г. П. Беспамятнов, Ю. А. Кропотов — Л.: Химия, 1985. — 528 с.

69. Федоренко А. М. Охрана труда в химии. Методические указания / А. М. Федоренко — Симферополь. — 2001. — 31 с.

70. Zhiyuan Z., Magnusson G. Synthesis of double-chain bis-sulfone neoglycolipids of the 2?-, 3?-, 4?-, and 6?-deoxyglobotrioses / Z. Zhiyuan, G. Magnusson // Carbohydr. Res. — 1994. — Vol. 262. — P. 79−101.

71. Mori M., Ito Y., Ogawa T. A highly stereoselective and practical synthesis of cyclomannohexaose, Cyclo {>4)-[б-D-Manp-(1>4)-] 5-б-D-Manp-(1>}, a manno isomer of cyclomaltohexaose / M. Mori, Y. Ito, T. Ogawa // Carbohydr. Res. — 1989. — Vol. 192. — P. 131−146.

72. Matsuzaki Y., Ito Y., Ogawa T. Stereoselective total synthesis of the blood group I-active biantennary neolacto-glycodecaosyl ceramide / Y. Matsuzaki, Y. Ito, T. Ogawa // Tetrahedron Lett. — 1992. — Vol. 33. — P. 4025−4028.

73. Dan A., Ito Y., Ogawa T. A Convergent and stereocontrolled synthetic route to the core pentasaccharide structure of asparagine-linked glycoproteins / A. Dan, Y. Ito, T. Ogawa // J. Org. Chem. — 1995. — Vol. 60. — P. 4680−4681.

74. Murakata C., Ogawa T. Stereoselective total synthesis of the glycosyl phosphatidylinositol (GPI) anchor of Trypanosoma brucei / C. Murakata, T. Ogawa // Carbohydr. Res. — 1992. — Vol. 235. — P. 95−114.

75. Cyclo-glycosylation of (1>4)-linked glycohexaoses: Synthesis of cyclo-lactohexaose / H. Kuyama, T. Nukada, Y. Nakahara, T. Ogawa // Tetrahedron Lett. — 1993. — Vol. 34. — P. 2171−2174.

76. Катализируемый краун-соединениями синтез в-арилгликозидов N-ацетилглюкозамина / В. О. Курьянов, Т. А. Чупахина, А. Е. Земляков, С. А. Котляр, Г. Л. Камалов, В. Я. Чирва [и др. ] // Биоорганическая химия. — 2001. — Т. 27, № 6. — С. 434−438.

77. Banoub J., Boullanger P., Lafont D. Synthesis of Oligosaccharides of 2-Amino-2-deoxy Sugars / J. Banoub, P. Boullanger, D. Lafont // Chem. Rev. — 1992. — Vol. 92, № 6. — P. 1167 — 1195.

78. Kiso M., Anderson L. Protected Glycosides and Dysaccharides of 2-amino-2-deoxy-D-glucopyranose by ferric chloride-catalyzed coupling / M. Kiso, L. Anderson // Carb. Res. — 1985. — P. 315 — 316.

79. Bergmann M., Zervas L. Synthesen mit Glucosamin / M. Bergmann, L. Zervas // Ber. deut. chem. Ges. — 1931. — Vol. 64. — P. 975−980.

80. Агрономов А. Е. Избранные главы органической химии: учеб. пособие. / А. Е. Агрономов. — М.: Химия, 1990. — 560 с.

81. Никольский Б. П. Справочник химика. / Б. П. Никольский. — М.: Химия, 1964. — 1168 с.

82. Synthesis and Crystal Structure of p-Methoxyphenyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-в-D-glucopyranoside / D. Peikow, A. Gessner, C.-M. Matern, G. Martin, A. Kelling [et al.] // Analytical Sciences. — 2006. — Vol. 22. — P. 975−980.

83. 4-(2-Chloroethoxy)phenyl group — novel anomeric protection with dual function / N. N. Kondakov, A. I. Zinin, A. M. Shpirt, P. I. Abronina [et al.] // 16th European Carbohydrate Symposium. — 2011. — PO 169. — P.383.

84. Synthesis of some 2-alkoxy glyco-[2,1-d]-2-oxazolines and evaluation of their glycosylation reactivity / S.S. Pertel, L.O. Kononov, A.I. Zinin [et al.] // Carb. Res. — 2012. — 10.10.16/j cararess 2012.03.026. принято к публикации.

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