메뉴 건너뛰기




Volumn 59, Issue , 2004, Pages 69-134

Synthesis and reactions of glycosides

Author keywords

[No Author keywords available]

Indexed keywords

ACID; BASE; GLYCOSIDE; SULFONE; SULFOXIDE; THIOGLYCOSIDE;

EID: 11144303670     PISSN: 00652318     EISSN: None     Source Type: Book Series    
DOI: 10.1016/S0065-2318(04)59003-0     Document Type: Review
Times cited : (55)

References (235)
  • 1
    • 0012465366 scopus 로고
    • Glycosides
    • W. Pigman and D. Horton (Eds.), Academic Press, New York and London
    • W. G. Overend, Glycosides, in W. Pigman and D. Horton (Eds.), The Carbohydrates, Chemistry and Biochemistry, Vol. IA, Academic Press, New York and London, 1972, pp. 279-346.
    • (1972) The Carbohydrates, Chemistry and Biochemistry , vol.1 A , pp. 279-346
    • Overend, W.G.1
  • 4
    • 84980113544 scopus 로고
    • Über die Glucoside der Alkohole
    • Fischer E. Über die Glucoside der Alkohole. Ber. 26:1893;2400-2412
    • (1893) Ber. , vol.26 , pp. 2400-2412
    • Fischer, E.1
  • 5
    • 84972798736 scopus 로고
    • Über die Verbindungen de Zucker mit den Alkoholen und Ketonen
    • Fischer E. Über die Verbindungen de Zucker mit den Alkoholen und Ketonen. Ber. 28:1895;1145-1168
    • (1895) Ber. , vol.28 , pp. 1145-1168
    • Fischer, E.1
  • 6
    • 0002727924 scopus 로고
    • Glycosidation of sugars. II. Methanolysis of D-xylose, D-lyxose, and D-ribose
    • Bishop C.T., Cooper F.P. Glycosidation of sugars. II. Methanolysis of D-xylose, D-lyxose, and D-ribose. Can. J. Chem. 41:1963;2743-2758
    • (1963) Can. J. Chem. , vol.41 , pp. 2743-2758
    • Bishop, C.T.1    Cooper, F.P.2
  • 7
    • 2442689627 scopus 로고
    • Action of strong acids on acetylated glycosides. V. Synthesis of β-isomaltose octaacetate
    • Lindberg B. Action of strong acids on acetylated glycosides. V. Synthesis of β-isomaltose octaacetate. Acta Chem. Scand. 3:1949;1355-1357
    • (1949) Acta Chem. Scand. , vol.3 , pp. 1355-1357
    • Lindberg, B.1
  • 10
    • 0016040837 scopus 로고
    • Results and problems of O-glycoside synthesis
    • Wulff G., Röhle G. Results and problems of O-glycoside synthesis. Angew. Chem. Int. Edn. Engl. 13:1974;157-170
    • (1974) Angew. Chem. Int. Edn. Engl. , vol.13 , pp. 157-170
    • Wulff, G.1    Röhle, G.2
  • 11
    • 0000880754 scopus 로고
    • The Koenigs-Knorr reaction
    • Igarashi K. The Koenigs-Knorr reaction. Adv. Carbohydr. Chem. 34:1977;243-283
    • (1977) Adv. Carbohydr. Chem. , vol.34 , pp. 243-283
    • Igarashi, K.1
  • 12
    • 0017831219 scopus 로고
    • Chemical synthesis of oligosaccharides
    • (Complex Carbohydrates, Part C)
    • H. M. Flowers. Chemical synthesis of oligosaccharides, Methods Enzymol., 50 (Complex Carbohydrates, Part C) (1978) 93-121.
    • (1978) Methods Enzymol. , vol.50 , pp. 93-121
    • Flowers, H.M.1
  • 13
    • 33846545444 scopus 로고
    • Haworth Memorial Lecture. Human blood groups and carbohydrate chemistry
    • Lemieux R.U. Haworth Memorial Lecture. Human blood groups and carbohydrate chemistry. Chem. Soc. Revs. 7:1978;423-452
    • (1978) Chem. Soc. Revs. , vol.7 , pp. 423-452
    • Lemieux, R.U.1
  • 15
    • 0040657616 scopus 로고
    • Advances in selective chemical synthesis of complex oligosaccharides
    • Paulsen H. Advances in selective chemical synthesis of complex oligosaccharides. Angew. Chem. Int. Edn. Engl. 21:1982;155-224
    • (1982) Angew. Chem. Int. Edn. Engl. , vol.21 , pp. 155-224
    • Paulsen, H.1
  • 16
    • 84956788420 scopus 로고
    • Preparation of glucosides from acetobromoglucose
    • Helferich B., Wedemeyer K.F. Preparation of glucosides from acetobromoglucose. Ann. 563:1949;139-145
    • (1949) Ann. , vol.563 , pp. 139-145
    • Helferich, B.1    Wedemeyer, K.F.2
  • 17
    • 84981753551 scopus 로고
    • The synthesis of glucosides and of nonreducing disaccharides
    • Helferich B., Weis K. The synthesis of glucosides and of nonreducing disaccharides. Chem. Ber. 89:1956;314-321
    • (1956) Chem. Ber. , vol.89 , pp. 314-321
    • Helferich, B.1    Weis, K.2
  • 18
    • 84981751431 scopus 로고
    • Synthesis of tetra-O-acetylhexoses with a free 2-hydroxyl group. Synthesis of disaccharides
    • Helferich B., Zirner J. Synthesis of tetra-O-acetylhexoses with a free 2-hydroxyl group. Synthesis of disaccharides. Chem. Ber. 95:1962;2604-2611
    • (1962) Chem. Ber. , vol.95 , pp. 2604-2611
    • Helferich, B.1    Zirner, J.2
  • 19
    • 11144335738 scopus 로고
    • Stereoselective synthesis of α-D-glucopyranosides
    • Lemieux R.U., Suemitsu R., Gunner G.S.W. Stereoselective synthesis of α-D-glucopyranosides. Can. J. Chem. 46:1968;1040-1041
    • (1968) Can. J. Chem. , vol.46 , pp. 1040-1041
    • Lemieux, R.U.1    Suemitsu, R.2    Gunner, G.S.W.3
  • 20
    • 0002746550 scopus 로고
    • Reaction of dimeric tri-O-acetyl-2-deoxy-2-nitroso-α-hexopyranosyl chlorides with alcohols
    • Lemieux R.U., Ito Y., James K., Nagabhushan T.L. Reaction of dimeric tri-O-acetyl-2-deoxy-2-nitroso-α-hexopyranosyl chlorides with alcohols. Can. J. Chem. 51:1973;7-18
    • (1973) Can. J. Chem. , vol.51 , pp. 7-18
    • Lemieux, R.U.1    Ito, Y.2    James, K.3    Nagabhushan, T.L.4
  • 21
    • 0002054596 scopus 로고
    • Reduction of isopropyl tri-O-acetyl-2-oximino-α-D-hexopyranosides
    • Lemieux R.U., James K., Nagabhushan T.L., Ito Y. Reduction of isopropyl tri-O-acetyl-2-oximino-α-D-hexopyranosides. Can. J. Chem. 51:1973;33-41
    • (1973) Can. J. Chem. , vol.51 , pp. 33-41
    • Lemieux, R.U.1    James, K.2    Nagabhushan, T.L.3    Ito, Y.4
  • 23
    • 0002479786 scopus 로고
    • Chemical synthesis of α-linked 2′-amino-2′- deoxydisaccharides
    • Lemieux R.U., James K., Nagabhushan T.L. Chemical synthesis of α-linked 2′-amino-2′-deoxydisaccharides. Can. J. Chem. 51:1973;48-52
    • (1973) Can. J. Chem. , vol.51 , pp. 48-52
    • Lemieux, R.U.1    James, K.2    Nagabhushan, T.L.3
  • 24
    • 0002545208 scopus 로고
    • Synthesis of derivatives of N-acetyl-D-lactosamine from D-lactal hexaacetate. Hexa-O-acetyl-2-deoxy-2-phthalimido-β-D-lactosyl chloride
    • Lemieux R.U., Abbas S.Z., Burzynska M.H., Ratcliffe R.M. Synthesis of derivatives of N-acetyl-D-lactosamine from D-lactal hexaacetate. Hexa-O-acetyl-2-deoxy-2-phthalimido-β-D-lactosyl chloride. Can. J. Chem. 60:1982;63-67
    • (1982) Can. J. Chem. , vol.60 , pp. 63-67
    • Lemieux, R.U.1    Abbas, S.Z.2    Burzynska, M.H.3    Ratcliffe, R.M.4
  • 25
    • 0000205069 scopus 로고
    • The azidonitration of tri-O-acetyl-D-galactal
    • Lemieux R.U., Ratcliffe R.M. The azidonitration of tri-O-acetyl-D- galactal. Can. J. Chem. 57:1979;1244-1251
    • (1979) Can. J. Chem. , vol.57 , pp. 1244-1251
    • Lemieux, R.U.1    Ratcliffe, R.M.2
  • 26
    • 33847801270 scopus 로고
    • Halide ion catalyzed glycosidation reactions. Syntheses of α-linked disaccharides
    • Lemieux R.U., Hendricks K.B., Stick R.V., James K. Halide ion catalyzed glycosidation reactions. Syntheses of α-linked disaccharides. J. Am. Chem. Soc. 97:1975;4056-4062
    • (1975) J. Am. Chem. Soc. , vol.97 , pp. 4056-4062
    • Lemieux, R.U.1    Hendricks, K.B.2    Stick, R.V.3    James, K.4
  • 28
    • 0034563416 scopus 로고    scopus 로고
    • A mechanistic study the nucleophilic dependence in glucosylations with glucosyl bromides
    • Bowden T., Garegg P.J., Konradsson P., Maloisel J.-L. A mechanistic study The nucleophilic dependence in glucosylations with glucosyl bromides. Israel J. Chem. 40:2001;271-277
    • (2001) Israel J. Chem. , vol.40 , pp. 271-277
    • Bowden, T.1    Garegg, P.J.2    Konradsson, P.3    Maloisel, J.-L.4
  • 29
    • 11144264407 scopus 로고
    • Chemical syntheses of 4-O-α and -β-D-galactopyranosyl-D- galactose and 3-O-α and -β-D-galactopyranosyl-D-galactose
    • Charnación M., Chacón-Fuertes M.E., Martin-Lomas M. Chemical syntheses of 4-O-α and -β-D-galactopyranosyl-D-galactose and 3-O-α and -β-D-galactopyranosyl-D-galactose. Carbohydr. Res. 43:1975;51-56
    • (1975) Carbohydr. Res. , vol.43 , pp. 51-56
    • Charnación, M.1    Chacón-Fuertes, M.E.2    Martin-Lomas, M.3
  • 30
    • 0008355447 scopus 로고
    • Building blocks for oligosaccharides. XV. Synthesis of β-D-mannopyranosyl- and 2-azido-2-deoxy-α-D-glucopyranosyl-containing disaccharide halide building blocks
    • H. Paulsen and O. Lockhoff, Building blocks for oligosaccharides. XV. Synthesis of β-D-mannopyranosyl- and 2-azido-2-deoxy-α-D- glucopyranosyl-containing disaccharide halide building blocks, Tetrahedron. Lett., (1978) 4027-4030.
    • (1978) Tetrahedron. Lett. , pp. 4027-4030
    • Paulsen, H.1    Lockhoff, O.2
  • 31
    • 0000999811 scopus 로고
    • Building units for oligosaccharides, IX. Stereoselective synthesis of α-glycosidically linked di- and oligosaccharides of 2-amino-2-deoxy-D- glucopyranose
    • Paulsen H., Stenzel W. Building units for oligosaccharides, IX. Stereoselective synthesis of α-glycosidically linked di- and oligosaccharides of 2-amino-2-deoxy-D-glucopyranose. Chem. Ber. 111:1978;2234-2347
    • (1978) Chem. Ber. , vol.111 , pp. 2234-2347
    • Paulsen, H.1    Stenzel, W.2
  • 32
    • 84980140202 scopus 로고
    • Building units for oligosaccharides, X. Synthesis of α-1→4 and α-1 → 3 linked disaccharides of 2-amino-2-deoxy-D-glucopyranose by the azide method
    • Paulsen H., Stenzel W. Building units for oligosaccharides, X. Synthesis of α-1→4 and α-1 → 3 linked disaccharides of 2-amino-2-deoxy-D-glucopyranose by the azide method. Chem. Ber. 111:1978;2348-2357
    • (1978) Chem. Ber. , vol.111 , pp. 2348-2357
    • Paulsen, H.1    Stenzel, W.2
  • 33
    • 84982495028 scopus 로고
    • Building units for oligosaccharides. XVI. Synthesis of the oligosaccharide determinants of the blood-group substances of type 1 of the ABH system
    • 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. Chem. Ber. 112:1979;3190-3202
    • (1979) Chem. Ber. , vol.112 , pp. 3190-3202
    • Paulsen, H.1    Kolar, C.2
  • 34
    • 0001687323 scopus 로고
    • A novel glucosidation reaction. Application to the synthesis of α-linked disaccharides
    • Pougny J.R., Nassr M.A.M., Naulet N., Sinaÿ P. A novel glucosidation reaction. Application to the synthesis of α-linked disaccharides. Nouv. J. Chim. 2:1978;389-395
    • (1978) Nouv. J. Chim. , vol.2 , pp. 389-395
    • Pougny, J.R.1    Nassr, M.A.M.2    Naulet, N.3    Sinaÿ, P.4
  • 35
    • 0018216477 scopus 로고
    • Recent advances in glycosylation reactions
    • Sinäy P. Recent advances in glycosylation reactions. Pure Appl. Chem. 50:1978;1437-1452
    • (1978) Pure Appl. Chem. , vol.50 , pp. 1437-1452
    • Sinäy, P.1
  • 36
    • 84985624827 scopus 로고
    • Simple syntheses of α- And β-O-glycosyl imidates; Preparation of glycosides and disaccharides
    • Schmidt R.R., Michel J. Simple syntheses of α- and β-O-glycosyl imidates; preparation of glycosides and disaccharides. Angew. Chem. Int. Edn. Engl. 19:1980;731-732
    • (1980) Angew. Chem. Int. Edn. Engl. , vol.19 , pp. 731-732
    • Schmidt, R.R.1    Michel, J.2
  • 37
    • 84981925686 scopus 로고
    • α-Linked disaccharides from O-(β-D-glucopyranosyl)- trichloroacetimidates using trimethylsilyltrifluoromethanesulfonate as catalyst
    • R. R. Schmidt and G. Grundler, α-Linked disaccharides from O-(β-D-glucopyranosyl)-trichloroacetimidates using trimethylsilyltrifluoromethanesulfonate as catalyst, Angew. Chem. Suppl., (1982) 1707-1715.
    • (1982) Angew. Chem. Suppl. , pp. 1707-1715
    • Schmidt, R.R.1    Grundler, G.2
  • 40
    • 0015870720 scopus 로고
    • Benzylated orthoesters in glycoside synthesis. The synthesis of alpha-D-glucopyranosides and beta-D-mannopyranosides
    • Borén H.B., Ekborg G., Eklind K., Garegg P.J., Pilotti Å., Swahn C.-G. Benzylated orthoesters in glycoside synthesis. The synthesis of alpha-D-glucopyranosides and beta-D-mannopyranosides. Acta Chem. Scand. 27:1973;2639-2644
    • (1973) Acta Chem. Scand. , vol.27 , pp. 2639-2644
    • Borén, H.B.1    Ekborg, G.2    Eklind, K.3    Garegg, P.J.4    Pilotti, Å.5    Swahn, C.-G.6
  • 41
    • 0001079749 scopus 로고
    • Oxidation of primary and secondary alcohols in partially protected sugars with the chromium trioxide-pyridine complex in the presence of acetic anhydride
    • 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. Carbohydr. Res. 67:1978;267-270
    • (1978) Carbohydr. Res. , vol.67 , pp. 267-270
    • Garegg, P.J.1    Samuelsson, B.2
  • 42
    • 0026576695 scopus 로고
    • 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
    • F. W. Lichtenthaler, U. Klaeres, M. Lergenmueller, and S. Schwidetzky, 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, Synthesis, (1992) 179-184.
    • (1992) Synthesis , pp. 179-184
    • Lichtenthaler, F.W.1    Klaeres, U.2    Lergenmueller, M.3    Schwidetzky, S.4
  • 43
    • 85008122324 scopus 로고
    • 2-Oxo- and 2-oximinoglycosyl halides: Versatile glycosyl donors for the construction of β-D-mannose and β-D-mannosamine-containing oligosaccharides
    • Kaji E., Lichtenthaler F.W. 2-Oxo- and 2-oximinoglycosyl halides: versatile glycosyl donors for the construction of β-D-mannose and β-D-mannosamine-containing oligosaccharides. Trends Glycosci. Glycotech. 5:1993;121-142
    • (1993) Trends Glycosci. Glycotech. , vol.5 , pp. 121-142
    • Kaji, E.1    Lichtenthaler, F.W.2
  • 44
    • 84982073225 scopus 로고
    • Building units for oligosaccharides. XXX. New effective β-glycoside synthesis of mannose glycosides. Syntheses of mannose containing oligosaccharides
    • Paulsen H., Lockhoff O. Building units for oligosaccharides. XXX. New effective β-glycoside synthesis of mannose glycosides. Syntheses of mannose containing oligosaccharides. Chem. Ber. 114:1981;3102-3114
    • (1981) Chem. Ber. , vol.114 , pp. 3102-3114
    • Paulsen, H.1    Lockhoff, O.2
  • 45
    • 0001095632 scopus 로고
    • Silver zeolite as promoter in glycoside synthesis. The synthesis of β-D-mannopyranosides
    • Garegg P.J., Ossowski P. Silver zeolite as promoter in glycoside synthesis. The synthesis of β-D-mannopyranosides. Act. Chem. Scand. B37:1983;249-250
    • (1983) Act. Chem. Scand. , vol.37 , pp. 249-250
    • Garegg, P.J.1    Ossowski, P.2
  • 46
    • 0001023062 scopus 로고
    • Configuration of glycosidic linkages in oligosaccharides. IX. Synthesis of α- And β-D-mannopyranosyl disaccharides
    • Gorin P.A.J., Perlin A.S. Configuration of glycosidic linkages in oligosaccharides. IX. Synthesis of α- and β-D-mannopyranosyl disaccharides. Can. J. Chem. 39:1961;2474-2485
    • (1961) Can. J. Chem. , vol.39 , pp. 2474-2485
    • Gorin, P.A.J.1    Perlin, A.S.2
  • 47
    • 0000330834 scopus 로고
    • Synthesis of 4-O-β-D-mannopyranosyl-L-rhamnopyranose
    • Bebault G.M., Dutton G.G.S. Synthesis of 4-O-β-D-mannopyranosyl-L- rhamnopyranose. Carbohydr. Res. 37:1974;309-319
    • (1974) Carbohydr. Res. , vol.37 , pp. 309-319
    • Bebault, G.M.1    Dutton, G.G.S.2
  • 48
    • 0041720045 scopus 로고
    • Synthesis of the pentasaccharide repeating unit of the O-specific polysaccharide from Salmonella strasbourg
    • Kochetkov N.K., Torgov V.L., Malysheva N.N., Shashkov A.S. Synthesis of the pentasaccharide repeating unit of the O-specific polysaccharide from Salmonella strasbourg. Tetrahedron. 36:1980;1099-1105
    • (1980) Tetrahedron , vol.36 , pp. 1099-1105
    • Kochetkov, N.K.1    Torgov, V.L.2    Malysheva, N.N.3    Shashkov, A.S.4
  • 49
    • 84988058248 scopus 로고
    • Practical synthesis of O-β-D-mannopyranosyl-, O-α-D- mannopyranosyl-, and O-β-D-glucopyranosyl-(1→4)-O-α-L- rhamnopyranosyl-(1 → 3)-D-galactoses
    • Betaneli V.I., Ovchinnikov M.V., Backinowsky L.V., Kochetkov N.K. Practical synthesis of O-β-D-mannopyranosyl-, O-α-D-mannopyranosyl-, and O-β-D-glucopyranosyl-(1→4)-O-α-L-rhamnopyranosyl-(1 → 3)-D-galactoses. Carbohydr. Res. 84:1980;211-214
    • (1980) Carbohydr. Res. , vol.84 , pp. 211-214
    • Betaneli, V.I.1    Ovchinnikov, M.V.2    Backinowsky, L.V.3    Kochetkov, N.K.4
  • 50
    • 84982058327 scopus 로고
    • Studies on glycoside synthesis. IX. Synthesis of β-D- mannopyranosides
    • Wulff G., Wichelhaus J. Studies on glycoside synthesis. IX. Synthesis of β-D-mannopyranosides. Chem. Ber. 112:1979;2847-2853
    • (1979) Chem. Ber. , vol.112 , pp. 2847-2853
    • Wulff, G.1    Wichelhaus, J.2
  • 51
    • 0001516205 scopus 로고
    • Synthesis of disaccharides containing β-D-mannopyranosyl groups
    • Garegg P.J., Iversen T., Johansson R. Synthesis of disaccharides containing β-D-mannopyranosyl groups. Acta Chem. Scand. B34:1980;505-508
    • (1980) Acta Chem. Scand. , vol.34 , pp. 505-508
    • Garegg, P.J.1    Iversen, T.2    Johansson, R.3
  • 52
    • 0032554064 scopus 로고    scopus 로고
    • Direct formation of β-mannopyranosides from thioglycosides
    • Crich D., Sun S. Direct formation of β-mannopyranosides from thioglycosides. J. Am. Chem. Soc. 120:1998;435-436
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 435-436
    • Crich, D.1    Sun, S.2
  • 53
    • 0000734076 scopus 로고    scopus 로고
    • Formation of β-mannopyranosides of primary alcohols using the sulfoxide method
    • Crich D., Sun S. Formation of β-mannopyranosides of primary alcohols using the sulfoxide method. J. Org. Chem. 61:1996;4506-4507
    • (1996) J. Org. Chem. , vol.61 , pp. 4506-4507
    • Crich, D.1    Sun, S.2
  • 54
    • 0030894278 scopus 로고    scopus 로고
    • Direct synthesis of β-mannopyranosides by the sulfoxide method
    • Crich D., Sun S. Direct synthesis of β-mannopyranosides by the sulfoxide method. J. Org. Chem. 62:1997;1198-1199
    • (1997) J. Org. Chem. , vol.62 , pp. 1198-1199
    • Crich, D.1    Sun, S.2
  • 55
    • 12044251810 scopus 로고
    • Synthesis of β-mannopyranosides by intramolecular aglycon delivery
    • Barresi F., Hindsgaul O. Synthesis of β-mannopyranosides by intramolecular aglycon delivery. J. Am. Chem. Soc. 113:1991;9376-9377
    • (1991) J. Am. Chem. Soc. , vol.113 , pp. 9376-9377
    • Barresi, F.1    Hindsgaul, O.2
  • 56
    • 33947093052 scopus 로고
    • Olefin homologation with titanium methylene compounds
    • Tebbe F.N., Parshall G.W., Reddy G.S. Olefin homologation with titanium methylene compounds. J. Am. Chem. Soc. 100:1978;3611-3613
    • (1978) J. Am. Chem. Soc. , vol.100 , pp. 3611-3613
    • Tebbe, F.N.1    Parshall, G.W.2    Reddy, G.S.3
  • 57
    • 84921177645 scopus 로고
    • Stereocontrolled synthesis of disaccharides via the temporary silicon connection
    • Stork G., Kim G. Stereocontrolled synthesis of disaccharides via the temporary silicon connection. J. Am. Chem. Soc. 114:1992;1087-1088
    • (1992) J. Am. Chem. Soc. , vol.114 , pp. 1087-1088
    • Stork, G.1    Kim, G.2
  • 58
    • 26844498306 scopus 로고
    • A new approach to stereoselective synthesis of β-mannosides
    • Ito Y., Ogawa T. A new approach to stereoselective synthesis of β-mannosides. Angew. Chem. Int. Ed. Eng. 33:1994;1765-1767
    • (1994) Angew. Chem. Int. Ed. Eng. , vol.33 , pp. 1765-1767
    • Ito, Y.1    Ogawa, T.2
  • 59
    • 0041370672 scopus 로고
    • Synthesis of oligosaccharides by the orthoester method
    • Kochetkov N.K., Bochkov A.F. Synthesis of oligosaccharides by the orthoester method. Methods Carbohydr. Chem. 6:1972;480-486
    • (1972) Methods Carbohydr. Chem. , vol.6 , pp. 480-486
    • Kochetkov, N.K.1    Bochkov, A.F.2
  • 61
    • 0001107882 scopus 로고    scopus 로고
    • First synthesis of β-D-Galf(1→4)GlcNAc, a structural unit attached O-glycosidically in glycoproteins of Trypanosoma cruzi
    • and references therein
    • Gallo-Rodriguez C., Varela O., de Lederkremer R.M. First synthesis of β-D-Galf(1→4)GlcNAc, a structural unit attached O-glycosidically in glycoproteins of Trypanosoma cruzi. J. Org. Chem. 61:1996;1886-1889. and references therein
    • (1996) J. Org. Chem. , vol.61 , pp. 1886-1889
    • Gallo-Rodriguez, C.1    Varela, O.2    De Lederkremer, R.M.3
  • 63
    • 0009506562 scopus 로고
    • Oxazoline synthesis of 1,2-trans-2-acetamido-2-deoxyglycosides. Glycosylation with methyl-(3,4,6-tri-O-acetyl-1,2-dideoxy-α-D- galactopyrano)-[2′,1′:4,5]-2-oxazoline
    • 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-α-D-galactopyrano)-[2′,1′:4,5]-2-oxazoline. Carbohydr. Res. 32:1974;137-143
    • (1974) Carbohydr. Res. , vol.32 , pp. 137-143
    • Jacquinet, J.-C.1    Zurabyan, S.E.2    Khorlin, A.A.3
  • 64
    • 0011912623 scopus 로고
    • Innovations in synthetic carbohydrate chemistry - Practical and conceptual approaches to glycoside synthesis
    • Hanessian S., Banoub J. Innovations in synthetic carbohydrate chemistry - practical and conceptual approaches to glycoside synthesis. Am. Chem. Soc. Symp. Ser. 39:1976;36-63
    • (1976) Am. Chem. Soc. Symp. Ser. , vol.39 , pp. 36-63
    • Hanessian, S.1    Banoub, J.2
  • 65
    • 0002374881 scopus 로고
    • Chemistry of the glycosidic linkage. An efficient synthesis of 1,2-trans-disaccharides
    • Hanessian S., Banoub J. Chemistry of the glycosidic linkage. An efficient synthesis of 1,2-trans-disaccharides. Carbohydr. Res. 53:1977;C13-C16
    • (1977) Carbohydr. Res. , vol.53
    • Hanessian, S.1    Banoub, J.2
  • 66
    • 0001937994 scopus 로고
    • Synthesis of 2-amino-2-deoxy-β-D-glucopyranosides. Properties and use of 2-deoxy-2-phthalimidoglycosyl halides
    • Lemieux R.U., Takeda T., Chung B.Y. Synthesis of 2-amino-2-deoxy-β- D-glucopyranosides. Properties and use of 2-deoxy-2-phthalimidoglycosyl halides. Am. Chem. Soc Symp. Ser. 39:1976;90-115
    • (1976) Am. Chem. Soc Symp. Ser. , vol.39 , pp. 90-115
    • Lemieux, R.U.1    Takeda, T.2    Chung, B.Y.3
  • 67
    • 0032546088 scopus 로고    scopus 로고
    • Use of Dichloropthaloyl (DCPhth) group as amino protection group in oligosaccharide synthesis
    • Legermüller M., Ito Y., Ogawa T. Use of Dichloropthaloyl (DCPhth) group as amino protection group in oligosaccharide synthesis. Tetrahedron. 54:1998;1381-1394
    • (1998) Tetrahedron , vol.54 , pp. 1381-1394
    • Legermüller, M.1    Ito, Y.2    Ogawa, T.3
  • 68
    • 0001735854 scopus 로고
    • Two new orthogonal amine-protecting groups that can be cleaved under mild or neutral conditions
    • Debenham J.S., Madsen R., Roberts C., Fraser-Reid B. Two new orthogonal amine-protecting groups that can be cleaved under mild or neutral conditions. J. Am. Chem. Soc. 117:1995;3302-3303
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 3302-3303
    • Debenham, J.S.1    Madsen, R.2    Roberts, C.3    Fraser-Reid, B.4
  • 69
    • 85047674110 scopus 로고
    • Glycoslimidates. 72. N-Tetrachlorophthaloyl-protected trichloroacetimidate of glucosamine as glycosyl donor in oligosaccharide synthesis
    • Castro-Palermo J.C., Schmidt R.R. Glycoslimidates. 72. N-Tetrachlorophthaloyl-protected trichloroacetimidate of glucosamine as glycosyl donor in oligosaccharide synthesis. Tetrahedron Lett. 36:1995;5343-5346
    • (1995) Tetrahedron Lett. , vol.36 , pp. 5343-5346
    • Castro-Palermo, J.C.1    Schmidt, R.R.2
  • 70
    • 0000275934 scopus 로고
    • Observations on silver trifluoromethane sulfonate-promoted syntheses of 1,2-trans-glycosides from acylated glycosyl bromides
    • Garegg P.J., Norberg T. Observations on silver trifluoromethane sulfonate-promoted syntheses of 1,2-trans-glycosides from acylated glycosyl bromides. Acta Chem. Scand. 33:1979;116-118
    • (1979) Acta Chem. Scand. , vol.33 , pp. 116-118
    • Garegg, P.J.1    Norberg, T.2
  • 72
    • 0034693085 scopus 로고    scopus 로고
    • The synthesis of 2-deoxyglycosides: 1988-1999
    • Marzabadi C.H., Franck R.W. The synthesis of 2-deoxyglycosides: 1988-1999. Tetrahedron. 56:2000;8385-8417
    • (2000) Tetrahedron , vol.56 , pp. 8385-8417
    • Marzabadi, C.H.1    Franck, R.W.2
  • 73
    • 0344902741 scopus 로고
    • New method for the deoxygenation of secondary alcohols
    • Barton D.H.R., McCombie S.W. New method for the deoxygenation of secondary alcohols. J. Chem. Soc. Perkin Trans. 1:1975;1574-1585
    • (1975) J. Chem. Soc. Perkin Trans. , vol.1 , pp. 1574-1585
    • Barton, D.H.R.1    McCombie, S.W.2
  • 74
    • 11144296623 scopus 로고
    • An efficient approach for the synthesis of 2-deoxy-β-D-glycosides
    • Gurjar M.K., Ghosh P.K. An efficient approach for the synthesis of 2-deoxy-β-D-glycosides. Indian J. Chem. Sect. B. 27:1988;1063-1064
    • (1988) Indian J. Chem. Sect. B. , vol.27 , pp. 1063-1064
    • Gurjar, M.K.1    Ghosh, P.K.2
  • 75
    • 0002710305 scopus 로고    scopus 로고
    • Convenient synthesis of α- and β-2-deoxyglycosides
    • J. C. Castro-Palomino and R. R. Schmidt, Convenient synthesis of α- and β-2-deoxyglycosides, Synlett., (1998) 501-503.
    • (1998) Synlett. , pp. 501-503
    • Castro-Palomino, J.C.1    Schmidt, R.R.2
  • 76
    • 0001432336 scopus 로고
    • The synthesis of β-D-glucopyranosyl 2-deoxy-α-D-arabino- hexopyranoside
    • Lemieux R.U., Morgan A.R. The synthesis of β-D-glucopyranosyl 2-deoxy-α-D-arabino- hexopyranoside. Can. J. Chem. 43:1965;2190-2198
    • (1965) Can. J. Chem. , vol.43 , pp. 2190-2198
    • Lemieux, R.U.1    Morgan, A.R.2
  • 77
    • 11144336397 scopus 로고
    • Reduction of chlorodeoxy sugars by tributyltin hydride
    • Arita H., Ueda N., Matsushima Y. Reduction of chlorodeoxy sugars by tributyltin hydride. Bull. Chem. Soc. Japan. 45:1972;567-569
    • (1972) Bull. Chem. Soc. Japan , vol.45 , pp. 567-569
    • Arita, H.1    Ueda, N.2    Matsushima, Y.3
  • 79
    • 84989568635 scopus 로고
    • Synthesis of α-linked 2′-deoxy-2′-iododisaccharides
    • J. Thiem, H. Karl, and J. Schwentner, Synthesis of α-linked 2′-deoxy-2′-iododisaccharides, Synthesis, (1978) 696-698.
    • (1978) Synthesis , pp. 696-698
    • Thiem, J.1    Karl, H.2    Schwentner, J.3
  • 80
    • 0019157694 scopus 로고
    • Syntheses with 2,6-dideoxyglycosyl halides. Construction of the B-A disaccharide glycoside in chromomycin A3
    • Thiem J., Meyer B. Syntheses with 2,6-dideoxyglycosyl halides. Construction of the B-A disaccharide glycoside in chromomycin A3. Chem. Ber. 113:1980;3058-3066
    • (1980) Chem. Ber. , vol.113 , pp. 3058-3066
    • Thiem, J.1    Meyer, B.2
  • 81
    • 0020353725 scopus 로고
    • Synthesis of cardiac glycosides: Evatromonoside and its anomer
    • Thiem J., Köpper S. Synthesis of cardiac glycosides: evatromonoside and its anomer. Angew. Chem. Int. Ed. Engl. 21:1982;779-780
    • (1982) Angew. Chem. Int. Ed. Engl. , vol.21 , pp. 779-780
    • Thiem, J.1    Köpper, S.2
  • 82
    • 0039587664 scopus 로고
    • Novel glycosylation reagents: Synthesis of disaccharides containing 2-deoxy-2-iodo-α-D-talopyranosyl groups
    • Garegg P.J., Samuelsson B., Konradsson P., Kvarnström I., Svensson S.C.T. Novel glycosylation reagents: synthesis of disaccharides containing 2-deoxy-2-iodo-α-D-talopyranosyl groups. Carbohydr. Res. 92:1981;157-159
    • (1981) Carbohydr. Res. , vol.92 , pp. 157-159
    • Garegg, P.J.1    Samuelsson, B.2    Konradsson, P.3    Kvarnström, I.4    Svensson, S.C.T.5
  • 83
    • 84982073225 scopus 로고
    • Building units for oligosaccharides. XXX. New effective β-glycoside synthesis of mannose glycosides. Syntheses of mannose containing oligosaccharides
    • Paulsen H., Lockhoff O. Building units for oligosaccharides. XXX. New effective β-glycoside synthesis of mannose glycosides. Syntheses of mannose containing oligosaccharides. Chem. Ber. 114:1981;3102-3114
    • (1981) Chem. Ber. , vol.114 , pp. 3102-3114
    • Paulsen, H.1    Lockhoff, O.2
  • 84
    • 58149406222 scopus 로고
    • Building blocks of oligosaccharides. XXXVIII. Synthesis of the branched tetrasaccharide building block of the key sequence of N-glycoproteins
    • Paulsen H., Lebuhn R., Lockoff O. Building blocks of oligosaccharides. XXXVIII. Synthesis of the branched tetrasaccharide building block of the key sequence of N-glycoproteins. Carbohydr. Res. 103:1982;C7-C11
    • (1982) Carbohydr. Res. , vol.103
    • Paulsen, H.1    Lebuhn, R.2    Lockoff, O.3
  • 85
    • 0000159086 scopus 로고
    • Progress in the selective chemical synthesis of complex oligosaccharides
    • Paulsen H. Progress in the selective chemical synthesis of complex oligosaccharides. Angew. Chem. 94:1982;184-201
    • (1982) Angew. Chem. , vol.94 , pp. 184-201
    • Paulsen, H.1
  • 86
    • 0001095632 scopus 로고
    • Silver zeolite as promoter in glycoside synthesis. The synthesis of β-D-mannopyranosides
    • Garegg P.J., Ossowski P. Silver zeolite as promoter in glycoside synthesis. The synthesis of β-D-mannopyranosides. Acta Chem. Scand. B37:1983;249-250
    • (1983) Acta Chem. Scand. , vol.37 , pp. 249-250
    • Garegg, P.J.1    Ossowski, P.2
  • 87
    • 0025649761 scopus 로고
    • Components of bacterial polysaccharides
    • Lindberg B. Components of bacterial polysaccharides. Adv. Carbohydr. Chem. Biochem. 48:1990;279-318
    • (1990) Adv. Carbohydr. Chem. Biochem. , vol.48 , pp. 279-318
    • Lindberg, B.1
  • 88
    • 0029978695 scopus 로고    scopus 로고
    • Synthesis of D-fructofuranosides using thioglycosides as glycosyl donors
    • and references therein
    • Krog-Jensen C., Oscarson S. Synthesis of D-fructofuranosides using thioglycosides as glycosyl donors. J. Org. Chem. 61:1996;1234-1238. and references therein
    • (1996) J. Org. Chem. , vol.61 , pp. 1234-1238
    • Krog-Jensen, C.1    Oscarson, S.2
  • 89
    • 0000504345 scopus 로고    scopus 로고
    • Synthesis of D-fructofuranosides using the internal aglycon delivery approach
    • and references therein
    • Krog-Jensen C., Oscarson S. Synthesis of D-fructofuranosides using the internal aglycon delivery approach. J. Org. Chem. 61:1996;4512-4513. and references therein
    • (1996) J. Org. Chem. , vol.61 , pp. 4512-4513
    • Krog-Jensen, C.1    Oscarson, S.2
  • 90
    • 0034692355 scopus 로고    scopus 로고
    • A novel β-directing fructofuranosyl concept. Stereospecific synthesis of sucrose
    • Oscarson S., Sehgelmeble F.W. A novel β-directing fructofuranosyl concept. Stereospecific synthesis of sucrose. J. Am. Chem. Soc. 122:2000;8869-8872
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 8869-8872
    • Oscarson, S.1    Sehgelmeble, F.W.2
  • 91
    • 0029163690 scopus 로고
    • Enzymes in organic synthesis: Application to the problems of carbohydrate recognition
    • Wong C.-H., Halcomb R.L., Ichikawa Y., Kajimoto T. Enzymes in organic synthesis: application to the problems of carbohydrate recognition. Angew. Chem. Int. Ed. Engl. 34:1995;521-546
    • (1995) Angew. Chem. Int. Ed. Engl. , vol.34 , pp. 521-546
    • Wong, C.-H.1    Halcomb, R.L.2    Ichikawa, Y.3    Kajimoto, T.4
  • 92
    • 0034505430 scopus 로고    scopus 로고
    • Syntheses of complex carbohydrates and glycoconjugates: Enzyme-based and programmable one-pot strategies
    • Koeller K.-M., Wong C.-H. Syntheses of complex carbohydrates and glycoconjugates: enzyme-based and programmable one-pot strategies. Chem. Rev. 100:2000;4465-4493
    • (2000) Chem. Rev. , vol.100 , pp. 4465-4493
    • Koeller, K.-M.1    Wong, C.-H.2
  • 93
    • 0029593613 scopus 로고
    • Synthesis of allyl and benzyl-β-D-glucopyranosides, and allyl-D-galactopyranoside from D-glucose or D-galactose and the corresponding alcohol using almond β-D-glucosidase
    • Vic G., Crout D.H.G. Synthesis of allyl and benzyl-β-D- glucopyranosides, and allyl-D-galactopyranoside from D-glucose or D-galactose and the corresponding alcohol using almond β-D-glucosidase. Carbohydr. Res. 279:1995;315-319
    • (1995) Carbohydr. Res. , vol.279 , pp. 315-319
    • Vic, G.1    Crout, D.H.G.2
  • 94
    • 0023656024 scopus 로고
    • A simple strategy for changing the regioselectivity of glycosidase-catalysed formation of disaccharides
    • Nilsson K.G.I. A simple strategy for changing the regioselectivity of glycosidase-catalysed formation of disaccharides. Carbohydr. Res. 167:1987;95-103
    • (1987) Carbohydr. Res. , vol.167 , pp. 95-103
    • Nilsson, K.G.I.1
  • 95
    • 0002766550 scopus 로고
    • A simple strategy for changing the regioselectivity of glycosidase-catalysed formation of disaccharides: Part II, Enzymic synthesis in situ of various acceptor glycosides
    • Nilsson K.G.I. A simple strategy for changing the regioselectivity of glycosidase-catalysed formation of disaccharides: Part II, Enzymic synthesis in situ of various acceptor glycosides. Carbohydr. Res. 180:1988;53-59
    • (1988) Carbohydr. Res. , vol.180 , pp. 53-59
    • Nilsson, K.G.I.1
  • 96
    • 0031484111 scopus 로고    scopus 로고
    • Syntheses of modified carbohydrates with glycosidases: Stereo- and regiospecific syntheses of lactosamine derivatives and related compounds
    • Nilsson K.G.I., Pan H., Larsson-Lorek U. Syntheses of modified carbohydrates with glycosidases: Stereo- and regiospecific syntheses of lactosamine derivatives and related compounds. J. Carbohydr. Chem. 16:1997;459-477
    • (1997) J. Carbohydr. Chem. , vol.16 , pp. 459-477
    • Nilsson, K.G.I.1    Pan, H.2    Larsson-Lorek, U.3
  • 97
    • 0015239679 scopus 로고
    • Two decades of research on the biosynthesis of saccharides
    • Leloir L.F. Two decades of research on the biosynthesis of saccharides. Science. 172:1971;1299-1303
    • (1971) Science , vol.172 , pp. 1299-1303
    • Leloir, L.F.1
  • 98
    • 0026512440 scopus 로고
    • Gram-scale synthesis of uridine 5′-diphospho-N-acetylglucosamine. Comparison of enzymatic and chemical routes
    • Heidlas J.E., Lees W.J., Pale P., Whitesides G.M. Gram-scale synthesis of uridine 5′-diphospho-N-acetylglucosamine. Comparison of enzymatic and chemical routes. J. Org. Chem. 146:1992;146-151
    • (1992) J. Org. Chem. , vol.146 , pp. 146-151
    • Heidlas, J.E.1    Lees, W.J.2    Pale, P.3    Whitesides, G.M.4
  • 99
    • 1642593650 scopus 로고
    • Enzyme-catalyzed synthesis of N-acetyllactosamine with in situ regeneration of uridine 5′-diphosphate glucose and uridine 5′-diphosphate galactose
    • Wong C.-H., Hayne S.L., Whitesides G.M. Enzyme-catalyzed synthesis of N-acetyllactosamine with in situ regeneration of uridine 5′-diphosphate glucose and uridine 5′-diphosphate galactose. J. Org. Chem. 47:1982;5416-5418
    • (1982) J. Org. Chem. , vol.47 , pp. 5416-5418
    • Wong, C.-H.1    Hayne, S.L.2    Whitesides, G.M.3
  • 102
    • 0034076318 scopus 로고    scopus 로고
    • Glycosidase inhibitors and their chemotherapeutic value, part 1
    • El Ashry E.S.H., Rashed N., Shobier A.H.S. Glycosidase inhibitors and their chemotherapeutic value, part 1. Pharmazie. 55:2000;251-262
    • (2000) Pharmazie , vol.55 , pp. 251-262
    • El Ashry, E.S.H.1    Rashed, N.2    Shobier, A.H.S.3
  • 103
    • 11144259150 scopus 로고
    • Method for producing non-reducing terminus-modified oligosaccharide derivatives
    • A. Hasegawa, M. Kiso, and S. Satomura, Method for producing non-reducing terminus-modified oligosaccharide derivatives, Jpn. Kokai Tokkyo Koho, (1995) 15 pp.
    • (1995) Jpn. Kokai Tokkyo Koho
    • Hasegawa, A.1    Kiso, M.2    Satomura, S.3
  • 104
    • 37849189010 scopus 로고    scopus 로고
    • Thioglycosides as glycosyl donors in oligosaccharide synthesis
    • Garegg P.J. Thioglycosides as glycosyl donors in oligosaccharide synthesis. Adv. Carbohydr. Chem. Biochem. 52:1997;179-205
    • (1997) Adv. Carbohydr. Chem. Biochem. , vol.52 , pp. 179-205
    • Garegg, P.J.1
  • 105
    • 0011945315 scopus 로고
    • 1-Thioglycosides
    • and references therein
    • Horton D. 1-Thioglycosides. Methods Carbohydr. Chem. 2:1963;368-373. and references therein
    • (1963) Methods Carbohydr. Chem. , vol.2 , pp. 368-373
    • Horton, D.1
  • 106
    • 0001729148 scopus 로고
    • 1-Thio-D-glucose
    • and references therein
    • Horton D. 1-Thio-D-glucose. Methods Carbohydr. Chem. 2:1963;433-437. and references therein
    • (1963) Methods Carbohydr. Chem. , vol.2 , pp. 433-437
    • Horton, D.1
  • 109
    • 0005790027 scopus 로고
    • The preparation of methyl α-L-thioarabinoside and of methyl β-D-thiogalactoside
    • Helferich B., Grünewald H., Langenhoff F. The preparation of methyl α-L-thioarabinoside and of methyl β-D-thiogalactoside. Chem. Ber. 86:1953;873-875
    • (1953) Chem. Ber. , vol.86 , pp. 873-875
    • Helferich, B.1    Grünewald, H.2    Langenhoff, F.3
  • 110
    • 0041721631 scopus 로고
    • Synthesis of para-substituted phenyl 1-thio-β-D-galactopyranosides
    • Yde M., De Bruyne C.K. Synthesis of para-substituted phenyl 1-thio-β-D-galactopyranosides. Carbohydr. Res. 26:1973;227-229
    • (1973) Carbohydr. Res. , vol.26 , pp. 227-229
    • Yde, M.1    De Bruyne, C.K.2
  • 111
    • 0002275678 scopus 로고
    • A novel 1,3 O → C silyl rearrangement in carbohydrate chemistry: Synthesis of α-D-glycopyranosyltrimethylsilanes
    • Pedretti V., Veyrières A., Sinäy P. A novel 1,3 O → C silyl rearrangement in carbohydrate chemistry: synthesis of α-D- glycopyranosyltrimethylsilanes. Tetrahedron. 46:1990;77-88
    • (1990) Tetrahedron , vol.46 , pp. 77-88
    • Pedretti, V.1    Veyrières, A.2    Sinäy, P.3
  • 112
    • 0001140515 scopus 로고
    • Stereoselective syntheses of O- and S-nitrophenyl glycosides. Part III. Syntheses in the α-D-galactopyranose and α-maltose series
    • Apparu M., Blanc-Muesser M., Defaye J., Driguez H. Stereoselective syntheses of O- and S-nitrophenyl glycosides. Part III. Syntheses in the α-D-galactopyranose and α-maltose series. Can. J. Chem. 59:1981;314-320
    • (1981) Can. J. Chem. , vol.59 , pp. 314-320
    • Apparu, M.1    Blanc-Muesser, M.2    Defaye, J.3    Driguez, H.4
  • 113
    • 0025908957 scopus 로고
    • Stereospecific synthesis of 1,2-trans-1-phenylthio-β-D-disaccharides under phase transfer catalysis
    • F. Tropper, F. O. Andersson, C. Grand-Maître, and R. Roy, Stereospecific synthesis of 1,2-trans-1-phenylthio-β-D-disaccharides under phase transfer catalysis, Synthesis, (1991) 734-736.
    • (1991) Synthesis , pp. 734-736
    • Tropper, F.1    Andersson, F.O.2    Grand-Maître, C.3    Roy, R.4
  • 114
    • 1542546914 scopus 로고
    • Developments in the chemistry of thio sugars
    • Horton D., Hutson D.H. Developments in the chemistry of thio sugars. Adv. Carbohydr. Chem. 18:1963;123-199
    • (1963) Adv. Carbohydr. Chem. , vol.18 , pp. 123-199
    • Horton, D.1    Hutson, D.H.2
  • 115
    • 0000448440 scopus 로고
    • S. H. Khan and R. A. O'Neill (Eds.), Harwood Academic Publishers, and references therein.
    • T. Norberg, in S. H. Khan and R. A. O'Neill (Eds.), Modern Methods in Carbohydrate Synthesis, Harwood Academic Publishers, 1995, pp. 82-106; and references therein.
    • (1995) Modern Methods in Carbohydrate Synthesis , pp. 82-106
    • Norberg, T.1
  • 116
    • 0001134853 scopus 로고
    • Stereoselective thioglycoside synthesis. Part XI. Zirconium(IV) chloride-catalyzed synthesis of 1,2-trans-1-thioglycopyranosides
    • Contour M.O., Defaye J., Little M., Wong E. Stereoselective thioglycoside synthesis. Part XI. Zirconium(IV) chloride-catalyzed synthesis of 1,2-trans-1-thioglycopyranosides. Carbohydr. Res. 193:1989;283-287
    • (1989) Carbohydr. Res. , vol.193 , pp. 283-287
    • Contour, M.O.1    Defaye, J.2    Little, M.3    Wong, E.4
  • 117
    • 0001591142 scopus 로고
    • Synthesis of ethyl and phenyl 1-thio-1,2-trans-D-glycopyranosides from the corresponding per-O-acetylated glycopyranoses having a 1,2-trans- configuration using anhydrous ferric chloride as a promoter
    • Dasgupta F., Garegg P.J. Synthesis of ethyl and phenyl 1-thio-1,2-trans-D-glycopyranosides from the corresponding per-O-acetylated glycopyranoses having a 1,2-trans-configuration using anhydrous ferric chloride as a promoter. Acta Chem. Scand. 43:1989;471-475
    • (1989) Acta Chem. Scand. , vol.43 , pp. 471-475
    • Dasgupta, F.1    Garegg, P.J.2
  • 118
    • 0001574318 scopus 로고
    • A new, stereoselective synthesis of methyl 1,2-trans-1-thioglycosides
    • Pozsgay V., Jennings H.J. A new, stereoselective synthesis of methyl 1,2-trans-1-thioglycosides. Tetrahedron Lett. 28:1987;1375-1376
    • (1987) Tetrahedron Lett. , vol.28 , pp. 1375-1376
    • Pozsgay, V.1    Jennings, H.J.2
  • 119
    • 37949003250 scopus 로고
    • A new approach to 1-thioglycosides by lowering the nucleophilicity of sulfur through trialkylstannylation
    • Ogawa T., Matsui M. A new approach to 1-thioglycosides by lowering the nucleophilicity of sulfur through trialkylstannylation. Carbohydr. Res. 54:1977;C17-C21
    • (1977) Carbohydr. Res. , vol.54
    • Ogawa, T.1    Matsui, M.2
  • 121
    • 0002167460 scopus 로고
    • Synthesis of 1,2-trans-related 1-thioglycoside esters
    • Ferrier R.J., Furneaux R. Synthesis of 1,2-trans-related 1-thioglycoside esters. Carbohydr. Res. 52:1976;63-68
    • (1976) Carbohydr. Res. , vol.52 , pp. 63-68
    • Ferrier, R.J.1    Furneaux, R.2
  • 122
    • 0000910927 scopus 로고
    • Mercaptolysis of glucose and galactose pentaacetates
    • Lemieux R.U. Mercaptolysis of glucose and galactose pentaacetates. Can. J. Chem. 29:1951;1079-1091
    • (1951) Can. J. Chem. , vol.29 , pp. 1079-1091
    • Lemieux, R.U.1
  • 123
    • 0011964976 scopus 로고
    • Comparison of the properties of the pentaacetates and methyl 1,2-orthoacetates of glucose and mannose
    • Lemieux R.U., Brice C. Comparison of the properties of the pentaacetates and methyl 1,2-orthoacetates of glucose and mannose. Can. J. Chem. 33:1955;109-119
    • (1955) Can. J. Chem. , vol.33 , pp. 109-119
    • Lemieux, R.U.1    Brice, C.2
  • 124
    • 11144285248 scopus 로고
    • Advances in the chemistry of thio sugars
    • M. L. Wolfrom and R. S. Tipson (Eds.), Academic Press, New York
    • D. Horton and D. H. Hutson, Advances in the chemistry of thio sugars, in M. L. Wolfrom and R. S. Tipson (Eds.), Advances in Carbohydrate Chemistry, Vol. 18, Academic Press, New York, 1963, p. 153.
    • (1963) Advances in Carbohydrate Chemistry , vol.18 , pp. 153
    • Horton, D.1    Hutson, D.H.2
  • 125
    • 0001401652 scopus 로고
    • A new method for the preparation of acetylated 1-thio-β-D- glucopyranosides
    • Černý M., Pacák J. A new method for the preparation of acetylated 1-thio-β-D-glucopyranosides. Collection Czech Chem. Commun. 24:1959;2566-2570
    • (1959) Collection Czech Chem. Commun. , vol.24 , pp. 2566-2570
    • Černý, M.1    Pacák, J.2
  • 126
    • 0028329871 scopus 로고
    • Reaction of sugar thiocyanates with Grignard reagents. New synthesis of thio glycosides
    • Pakulski Z., Pierozynski D., Zamojski A. Reaction of sugar thiocyanates with Grignard reagents. New synthesis of thio glycosides. Tetrahedron. 50:1994;2975-2992
    • (1994) Tetrahedron , vol.50 , pp. 2975-2992
    • Pakulski, Z.1    Pierozynski, D.2    Zamojski, A.3
  • 127
    • 37949053238 scopus 로고
    • Preparation of acetylated aromatic 1-thio-β-D-glucopyranosides from 2,3,4,6-tetra-O-acetyl-1-thio-β-D-glucopyranose and diazonium salts
    • Černý M., Zachystalova D., Pacák J. Preparation of acetylated aromatic 1-thio-β-D-glucopyranosides from 2,3,4,6-tetra-O- acetyl-1-thio-β-D-glucopyranose and diazonium salts. J. Coll. Czech Chem. Commun. 26:1961;2206-2211
    • (1961) J. Coll. Czech Chem. Commun. , vol.26 , pp. 2206-2211
    • Černý, M.1    Zachystalova, D.2    Pacák, J.3
  • 128
    • 11144320210 scopus 로고
    • Free-radical addition of 1-thiosugars to alkenes. A new general approach to the synthesis of 1-thioglycosides
    • Lacombe J.M., Rakotomanomana N., Pavia A.A. Free-radical addition of 1-thiosugars to alkenes. A new general approach to the synthesis of 1-thioglycosides. Tetrahedron Lett. 29:1988;4239-4296
    • (1988) Tetrahedron Lett. , vol.29 , pp. 4239-4296
    • Lacombe, J.M.1    Rakotomanomana, N.2    Pavia, A.A.3
  • 129
    • 37949053994 scopus 로고
    • Synthesis and reactions of glycosyl methyl- and benzyl xanthates. A facile synthesis of 1-thioglycosides
    • Sakata M., Haga M., Tejima S. Synthesis and reactions of glycosyl methyl- and benzyl xanthates. A facile synthesis of 1-thioglycosides. Carbohydr. Res. 13:1970;379-390
    • (1970) Carbohydr. Res. , vol.13 , pp. 379-390
    • Sakata, M.1    Haga, M.2    Tejima, S.3
  • 130
    • 0011248182 scopus 로고
    • Synthesis of S-glycosyl xanthates by phase transfer catalyzed substitution of glycosyl halides
    • Tropper F.D., Andersson F.O., Cao S., Roy R. Synthesis of S-glycosyl xanthates by phase transfer catalyzed substitution of glycosyl halides. J. Carbohydr. Chem. 11:1992;741-750
    • (1992) J. Carbohydr. Chem. , vol.11 , pp. 741-750
    • Tropper, F.D.1    Andersson, F.O.2    Cao, S.3    Roy, R.4
  • 131
    • 0000804018 scopus 로고
    • Synthesis of glycosyl xanthates from reducing sugar derivatives under phase-transfer conditions
    • Szeja W., Bogusiak J. Synthesis of glycosyl xanthates from reducing sugar derivatives under phase-transfer conditions. Carbohydr. Res. 170:1987;235-239
    • (1987) Carbohydr. Res. , vol.170 , pp. 235-239
    • Szeja, W.1    Bogusiak, J.2
  • 132
    • 0011964976 scopus 로고
    • Comparison of the properties of the pentaacetates and methyl 1,2-orthoacetates of glucose and mannose
    • Lemieux R.U., Brice C. Comparison of the properties of the pentaacetates and methyl 1,2-orthoacetates of glucose and mannose. Can. J. Chem. 33:1955;109-119
    • (1955) Can. J. Chem. , vol.33 , pp. 109-119
    • Lemieux, R.U.1    Brice, C.2
  • 134
    • 37049094782 scopus 로고
    • The reaction of some cyclic and open-chain disulfides with methyl trifluoromethanesulfonate
    • Ravenscroft M., Roberts R.M.G., Tillett J.G. The reaction of some cyclic and open-chain disulfides with methyl trifluoromethanesulfonate. J. Chem. Soc. Perkin Trans. 2:1982;1569-1572
    • (1982) J. Chem. Soc. Perkin Trans. , vol.2 , pp. 1569-1572
    • Ravenscroft, M.1    Roberts, R.M.G.2    Tillett, J.G.3
  • 135
    • 9844249084 scopus 로고
    • A novel promoter for the efficient construction of 1,2-trans linkages in glycoside synthesis, using thioglycosides as glycosyl donors
    • Fügedi P., Garegg P.J. A novel promoter for the efficient construction of 1,2-trans linkages in glycoside synthesis, using thioglycosides as glycosyl donors. Carbohydr. Res. 149:1986;C9-C12
    • (1986) Carbohydr. Res. , vol.149
    • Fügedi, P.1    Garegg, P.J.2
  • 136
    • 0001102301 scopus 로고
    • Synthesis of 1,2-cis-linked glycosides using dimethyl(methylthio) sulfonium triflate as promoter and thioglycosides as glycosyl donors
    • Andersson F.O., Fügedi P., Garegg P.J., Nashed M. Synthesis of 1,2-cis-linked glycosides using dimethyl(methylthio)sulfonium triflate as promoter and thioglycosides as glycosyl donors. Tetrahedron Lett. 27:1986;3919-3922
    • (1986) Tetrahedron Lett. , vol.27 , pp. 3919-3922
    • Andersson, F.O.1    Fügedi, P.2    Garegg, P.J.3    Nashed, M.4
  • 138
    • 0000937526 scopus 로고
    • An efficient glucosylation of alcohols using 1-thioglucoside derivative
    • T. Mukaiyama, T. Nakatsuka, and S. Shoda, An efficient glucosylation of alcohols using 1-thioglucoside derivative, Chem. Lett., (1979) 487-490.
    • (1979) Chem. Lett. , pp. 487-490
    • Mukaiyama, T.1    Nakatsuka, T.2    Shoda, S.3
  • 139
    • 34548501092 scopus 로고
    • Reinvestigation of the preparation of cholestereryl 2,3,4,6.-tetra-O- benzyl-α-D-glucopyranoside
    • van Cleve J.W. Reinvestigation of the preparation of cholestereryl 2,3,4,6.-tetra-O-benzyl-α-D-glucopyranoside. Carbohydr. Res. 70:1979;161-164
    • (1979) Carbohydr. Res. , vol.70 , pp. 161-164
    • Van Cleve, J.W.1
  • 140
    • 0002631391 scopus 로고
    • Chemistry of the glycosidic linkage. Exceptionally fast and efficient formation of glycosides by remote activation
    • Hanessian S., Bacquet C., Lehong N. Chemistry of the glycosidic linkage. Exceptionally fast and efficient formation of glycosides by remote activation. Carbohydr. Res. 80:1980;C17-C22
    • (1980) Carbohydr. Res. , vol.80
    • Hanessian, S.1    Bacquet, C.2    Lehong, N.3
  • 142
    • 0021081935 scopus 로고
    • Total synthesis of oleandrose and the avermectin disaccharide, benzyl α-L-oleandrosyl-α-L-4-acetoxyoleandroside
    • Wuts P.G.M., Bigelow S.S. Total synthesis of oleandrose and the avermectin disaccharide, benzyl α-L-oleandrosyl-α-L-4- acetoxyoleandroside. J. Org. Chem. 48:1983;3489-3493
    • (1983) J. Org. Chem. , vol.48 , pp. 3489-3493
    • Wuts, P.G.M.1    Bigelow, S.S.2
  • 143
    • 33845551357 scopus 로고
    • A mild and general method for the synthesis of O-glycosides
    • Nicolaou K.C., Seitz S.P., Papahatjis D.P. A mild and general method for the synthesis of O-glycosides. J. Am. Chem. Soc. 105:1983;2430-2434
    • (1983) J. Am. Chem. Soc. , vol.105 , pp. 2430-2434
    • Nicolaou, K.C.1    Seitz, S.P.2    Papahatjis, D.P.3
  • 144
    • 0000034767 scopus 로고
    • A reinvestigation of glycosidation reactions using 1-thioglycosides as glycosyl donors and thiophilic cations as promoters
    • Garegg P.J., Norberg T. A reinvestigation of glycosidation reactions using 1-thioglycosides as glycosyl donors and thiophilic cations as promoters. Carbohydr. Res. 116:1983;162-165
    • (1983) Carbohydr. Res. , vol.116 , pp. 162-165
    • Garegg, P.J.1    Norberg, T.2
  • 145
    • 0021168718 scopus 로고
    • A stereoselective synthesis of digitoxin. On cardioactive steroids XIII
    • Tsai T.Y.R., Jin H., Wiesner K. A stereoselective synthesis of digitoxin. On cardioactive steroids XIII. Can. J. Chem. 62:1984;1403-1405
    • (1984) Can. J. Chem. , vol.62 , pp. 1403-1405
    • Tsai, T.Y.R.1    Jin, H.2    Wiesner, K.3
  • 147
    • 0022426354 scopus 로고
    • Synthesis of a tri- and a hepta-saccharide which contain α-L-fucopyranosyl groups and are part of the complex type of carbohydrate moiety of glycoproteins
    • Lönn H. Synthesis of a tri- and a hepta-saccharide which contain α-L-fucopyranosyl groups and are part of the complex type of carbohydrate moiety of glycoproteins. Carbohydr. Res. 139:1985;105-113
    • (1985) Carbohydr. Res. , vol.139 , pp. 105-113
    • Lönn, H.1
  • 148
    • 0022426280 scopus 로고
    • Synthesis of a tetra- and a nona-saccharide which contain α-L-fucopyranosyl groups and are part of the complex type of carbohydrate moiety of glycoproteins
    • Lönn H. Synthesis of a tetra- and a nona-saccharide which contain α-L-fucopyranosyl groups and are part of the complex type of carbohydrate moiety of glycoproteins. Carbohydr. Res. 139:1985;115-121
    • (1985) Carbohydr. Res. , vol.139 , pp. 115-121
    • Lönn, H.1
  • 149
    • 84857776335 scopus 로고
    • Glycosylation using a thioglycoside and methyl trifluoromethanesufonate. A new and efficient method for cis and trans glycoside formation
    • Lönn H. Glycosylation using a thioglycoside and methyl trifluoromethanesufonate. A new and efficient method for cis and trans glycoside formation. J. Carbohydr. Chem. 6:1987;301-306
    • (1987) J. Carbohydr. Chem. , vol.6 , pp. 301-306
    • Lönn, H.1
  • 150
    • 33845281881 scopus 로고
    • A new method for the synthesis of O-glycosides from S-glycosides
    • Pozsgay V., Jennings H.J. A new method for the synthesis of O-glycosides from S-glycosides. J. Org. Chem. 52:1987;4635-4637
    • (1987) J. Org. Chem. , vol.52 , pp. 4635-4637
    • Pozsgay, V.1    Jennings, H.J.2
  • 151
    • 33845278293 scopus 로고
    • Synthetic oligosaccharides related to group B streptococcal polysaccharides. 3. Synthesis of oligosaccharides corresponding to the common polysaccharide antigen of group B streptococci
    • Pozsgay V., Jennings H.J. Synthetic oligosaccharides related to group B streptococcal polysaccharides. 3. Synthesis of oligosaccharides corresponding to the common polysaccharide antigen of group B streptococci. J. Org. Chem. 53:1988;4042-4052
    • (1988) J. Org. Chem. , vol.53 , pp. 4042-4052
    • Pozsgay, V.1    Jennings, H.J.2
  • 152
    • 0002879808 scopus 로고
    • Alkyl sulfenyl triflate as activator in the thioglycoside-mediated formation of glycosidic linkages during oligosaccharide synthesis
    • Dasgupta F., Garegg P.J. Alkyl sulfenyl triflate as activator in the thioglycoside-mediated formation of glycosidic linkages during oligosaccharide synthesis. Carbohydr. Res. 177:1988;C13-C17
    • (1988) Carbohydr. Res. , vol.177
    • Dasgupta, F.1    Garegg, P.J.2
  • 153
    • 0001047747 scopus 로고
    • Novel highly stereospecific method of 1,2-cis-glycosylation. Synthesis of α-D-glucosyl-D-glucoses
    • Kochetkov N.K., Klimov E.M., Malysheva N.N. Novel highly stereospecific method of 1,2-cis-glycosylation. Synthesis of α-D-glucosyl-D-glucoses. Tetrahedron Lett. 30:1989;5459-5462
    • (1989) Tetrahedron Lett. , vol.30 , pp. 5459-5462
    • Kochetkov, N.K.1    Klimov, E.M.2    Malysheva, N.N.3
  • 155
    • 0000573694 scopus 로고
    • A mild general method for the synthesis of α-linked disaccharides
    • Reddy G.V., Kulkarni V.R., Mereyala H.B. A mild general method for the synthesis of α-linked disaccharides. Tetrahedron Lett. 30:1989;4283-4286
    • (1989) Tetrahedron Lett. , vol.30 , pp. 4283-4286
    • Reddy, G.V.1    Kulkarni, V.R.2    Mereyala, H.B.3
  • 156
    • 0025125757 scopus 로고
    • Iodonium ion promoted reactions at the anomeric centers. II. An efficient thioglycoside mediated approach toward the formation of 1,2-trans-linked glycosides and glycosidic esters
    • Veeneman G.H., van Leeuwen S.H., van Boom J.H. Iodonium ion promoted reactions at the anomeric centers. II. An efficient thioglycoside mediated approach toward the formation of 1,2-trans-linked glycosides and glycosidic esters. Tetrahedron Lett. 31:1990;1331-1334
    • (1990) Tetrahedron Lett. , vol.31 , pp. 1331-1334
    • Veeneman, G.H.1    Van Leeuwen, S.H.2    Van Boom, J.H.3
  • 157
  • 158
    • 0025068837 scopus 로고
    • An efficient thioglycoside-mediated formation of α-glycosidic linkages promoted by iodonium dicollidine perchlorate
    • Veneman G.H., van Boom J.H. An efficient thioglycoside-mediated formation of α-glycosidic linkages promoted by iodonium dicollidine perchlorate. Tetrahedron Lett. 31:1990;275-278
    • (1990) Tetrahedron Lett. , vol.31 , pp. 275-278
    • Veneman, G.H.1    Van Boom, J.H.2
  • 160
    • 84987536027 scopus 로고
    • Glycosylation using of one-electron-transfer homogeneous reagent: A novel and efficient synthesis of β-linked disaccharides
    • A. Marra, J.-M. Mallet, C. Amatoreand, and P. Sinaÿ, Glycosylation using of one-electron-transfer homogeneous reagent: a novel and efficient synthesis of β-linked disaccharides, Synlett, (1990) 572-574.
    • (1990) Synlett , pp. 572-574
    • Marra, A.1    Mallet, J.-M.2    Amatoreand, C.3    Sinaÿ, P.4
  • 162
    • 0021135638 scopus 로고
    • L Practical synthesis of oligosaccharides. Partial synthesis of avermectin B1a
    • Nicolaou K.C., Dolle R.E., Papahatjis D.P., Randall J. L Practical synthesis of oligosaccharides. Partial synthesis of avermectin B1a. J. Am. Chem. Soc. 106:1984;4189-4192
    • (1984) J. Am. Chem. Soc. , vol.106 , pp. 4189-4192
    • Nicolaou, K.C.1    Dolle, R.E.2    Papahatjis, D.P.3    Randall, J.4
  • 163
    • 0000424679 scopus 로고
    • Syntheses of a heptasaccharide β-linked to an 8-methoxycarbonyl-oct- 1-yl linking arm amd of a decasaccharide with structures corresponding to the phytoelicitor active glucan of Phytophthora megasperma F.Sp. glycinea
    • Birberg W., Fügedi P., Garegg P.J., Pilotti Å. Syntheses of a heptasaccharide β-linked to an 8-methoxycarbonyl-oct-1-yl linking arm amd of a decasaccharide with structures corresponding to the phytoelicitor active glucan of Phytophthora megasperma F.Sp. glycinea. J. Carbohydr. Chem. 8:1989;47-57
    • (1989) J. Carbohydr. Chem. , vol.8 , pp. 47-57
    • Birberg, W.1    Fügedi, P.2    Garegg, P.J.3    Pilotti, Å.4
  • 164
    • 0028186224 scopus 로고
    • Anomeric oxygen-activation for glycoside synthesis: The trichloroacetimidate method
    • Schmidt R.R., Kinzy W. Anomeric oxygen-activation for glycoside synthesis: the trichloroacetimidate method. Adv. Carbohydr. Chem. Biochem. 50:1994;21-123
    • (1994) Adv. Carbohydr. Chem. Biochem. , vol.50 , pp. 21-123
    • Schmidt, R.R.1    Kinzy, W.2
  • 165
    • 33751386390 scopus 로고
    • Novel glycosidation methodology. The use of phenyl selenoglycosides as glycosyl donors and acceptors in oligosaccharide synthesis
    • Mehta S., M Pinto B. Novel glycosidation methodology. The use of phenyl selenoglycosides as glycosyl donors and acceptors in oligosaccharide synthesis. J. Org. Chem. 58:1993;3269-3276
    • (1993) J. Org. Chem. , vol.58 , pp. 3269-3276
    • Mehta, S.1    Pinto, B.M.2
  • 168
    • 0000508254 scopus 로고
    • Glycosylation on the Merrifield resin using anomeric sulfoxides
    • Yan L., Taylor C.M., Goodnow R. Jr., Kahne D. Glycosylation on the Merrifield resin using anomeric sulfoxides. J. Am. Chem. Soc. 116:1994;6953-6954
    • (1994) J. Am. Chem. Soc. , vol.116 , pp. 6953-6954
    • Yan, L.1    Taylor, C.M.2    Goodnow Jr., R.3    Kahne, D.4
  • 169
    • 0029904583 scopus 로고    scopus 로고
    • Generalizing glycosylation. Synthesis of the blood group antigens Lea, Leb, and Lex using a standard set of reaction conditions
    • Yan L., Kahne D. Generalizing glycosylation. Synthesis of the blood group antigens Lea, Leb, and Lex using a standard set of reaction conditions. J. Am. Chem. Soc. 118:1996;9239-9248
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 9239-9248
    • Yan, L.1    Kahne, D.2
  • 170
    • 0001329442 scopus 로고
    • Preparation of cyclic acetals from 2-benzenesulphonyl derivatives: A new, mild glycosylation procedure
    • Brown D.S., Ley S.V., Vile S. Preparation of cyclic acetals from 2-benzenesulphonyl derivatives: a new, mild glycosylation procedure. Tetrahedron Lett. 29:1988;4873-4876
    • (1988) Tetrahedron Lett. , vol.29 , pp. 4873-4876
    • Brown, D.S.1    Ley, S.V.2    Vile, S.3
  • 171
    • 0034200007 scopus 로고    scopus 로고
    • A glycosylation protocol based on activation of glycosyl 2-pyridyl sulfones with samarium triflate
    • Chang G.X., Lowary T.L., Todd L. A glycosylation protocol based on activation of glycosyl 2-pyridyl sulfones with samarium triflate. Org. Lett. 2:2000;1505-1508
    • (2000) Org. Lett. , vol.2 , pp. 1505-1508
    • Chang, G.X.1    Lowary, T.L.2    Todd, L.3
  • 172
    • 0025823547 scopus 로고
    • Phenyl selenoglycosides as novel, versatile glycosyl donors selective activation over thiglycosides
    • Mehta S., Pinto B.M. Phenyl selenoglycosides as novel, versatile glycosyl donors selective activation over thiglycosides. Tetrahedron Lett. 32:1991;4435-4438
    • (1991) Tetrahedron Lett. , vol.32 , pp. 4435-4438
    • Mehta, S.1    Pinto, B.M.2
  • 173
    • 33751386390 scopus 로고
    • Novel glycosidation methodology. The use of phenyl selenoglycosides as glycosyl donors and acceptors in oligosaccharide synthesis
    • Mehta S., Pinto B.M. Novel glycosidation methodology. The use of phenyl selenoglycosides as glycosyl donors and acceptors in oligosaccharide synthesis. J. Org. Chem. 58:1993;3269-3276
    • (1993) J. Org. Chem. , vol.58 , pp. 3269-3276
    • Mehta, S.1    Pinto, B.M.2
  • 174
    • 0342485364 scopus 로고    scopus 로고
    • Phenyl selenoglycosides as versatile glycosylating agents in oligosaccharide synthesis and the chemical synthesis of disaccharides containing sulfur and selenium
    • (S. H. Khan and R. A. O'Neill, Eds.), and references therein. Harwood Academic Publishers
    • S. Mehta and B. M. Pinto, Phenyl selenoglycosides as versatile glycosylating agents in oligosaccharide synthesis and the chemical synthesis of disaccharides containing sulfur and selenium, Front. Nat. Prod. Res., 1, Modern Methods in Carbohydrate Synthesis (S. H. Khan and R. A. O'Neill, Eds.), and references therein. Harwood Academic Publishers (1996, pp. 107-129).
    • (1996) Front. Nat. Prod. Res., 1, Modern Methods in Carbohydrate Synthesis , pp. 107-129
    • Mehta, S.1    Pinto, B.M.2
  • 176
    • 0031500701 scopus 로고    scopus 로고
    • O-Glycosidation of telluroglycoside by electrochemical oxidation
    • S. Yamago, K. Kokubo, and J. Yoshida, O-Glycosidation of telluroglycoside by electrochemical oxidation, Chem. Lett., (1997) 111-112.
    • (1997) Chem. Lett. , pp. 111-112
    • Yamago, S.1    Kokubo, K.2    Yoshida, J.3
  • 177
    • 0032558666 scopus 로고    scopus 로고
    • Glycosylation with telluroglycosides. Stereoselective construction of α- And β-anomers
    • Yamago S., Kokubo K., Murakami H., Mino Y., Haraand O., Yoshida J. Glycosylation with telluroglycosides. Stereoselective construction of α- and β-anomers. Tetrahedron Lett. 39:1998;7905-7908
    • (1998) Tetrahedron Lett. , vol.39 , pp. 7905-7908
    • Yamago, S.1    Kokubo, K.2    Murakami, H.3    Mino, Y.4    Haraand, O.5    Yoshida, J.6
  • 178
    • 0012850016 scopus 로고    scopus 로고
    • The selective activation of telluro- over seleno-β-D- glucopyranosides as glycosyl donors: A reactivity scale for various telluro, seleno and thio sugars
    • Stick R.V., Tilbrook D., Matthew G., Williams S.J. The selective activation of telluro- over seleno-β-D-glucopyranosides as glycosyl donors: a reactivity scale for various telluro, seleno and thio sugars. Aust. J. Chem. 50:1997;237-240
    • (1997) Aust. J. Chem. , vol.50 , pp. 237-240
    • Stick, R.V.1    Tilbrook, D.2    Matthew, G.3    Williams, S.J.4
  • 179
    • 0033521089 scopus 로고    scopus 로고
    • Preparation of glycosyl fluorides from phenyl 1-seleno- and phenyl 1-telluroglycosides
    • Horne G., Mackie W. Preparation of glycosyl fluorides from phenyl 1-seleno- and phenyl 1-telluroglycosides. Tetrahedron Lett. 40:1999;8697-8700
    • (1999) Tetrahedron Lett. , vol.40 , pp. 8697-8700
    • Horne, G.1    Mackie, W.2
  • 181
    • 0008629278 scopus 로고
    • Chemical synthesis of sucrose. A conformational analysis of the reactions of 1,2-anhydro-α-D-glucopyranose triacetate
    • Lemieux R.U., Huber G.A. Chemical synthesis of sucrose. A conformational analysis of the reactions of 1,2-anhydro-α-D-glucopyranose triacetate. J. Am. Chem. Soc. 78:1956;4117-4119
    • (1956) J. Am. Chem. Soc. , vol.78 , pp. 4117-4119
    • Lemieux, R.U.1    Huber, G.A.2
  • 182
    • 0016716244 scopus 로고
    • Synthesis of heparin saccharides IV, Synthesis of disaccharides possessing the structure of a repeating unit of heparin
    • Wyss P.C., Kiss J., Arnold W. Synthesis of heparin saccharides IV, Synthesis of disaccharides possessing the structure of a repeating unit of heparin. Helv. Chim. Acta. 58:1975;1847-1864
    • (1975) Helv. Chim. Acta. , vol.58 , pp. 1847-1864
    • Wyss, P.C.1    Kiss, J.2    Arnold, W.3
  • 183
    • 0000092870 scopus 로고
    • Synthesis of 1,2-anhydro-3,4,6-tri-O-benzyl-β-D-mannopyranose
    • Sondheimer S.J., Yamaguchi H., Schuerch C. Synthesis of 1,2-anhydro-3,4,6-tri-O-benzyl-β-D-mannopyranose. Carbohydr. Res. 74:1979;327-332
    • (1979) Carbohydr. Res. , vol.74 , pp. 327-332
    • Sondheimer, S.J.1    Yamaguchi, H.2    Schuerch, C.3
  • 184
    • 0343201956 scopus 로고
    • Chemical synthesis of a (1→2)-D-glucopyranan
    • Sherkey P.F., Eby R., Schuerch C. Chemical synthesis of a (1→2)-D-glucopyranan. Carbohydr. Res. 96:1981;223-229
    • (1981) Carbohydr. Res. , vol.96 , pp. 223-229
    • Sherkey, P.F.1    Eby, R.2    Schuerch, C.3
  • 185
    • 33845184508 scopus 로고
    • On the direct epoxidation of glycals: Application of a reiterative strategy for the synthesis of β-linked oligosaccharides
    • Halcomb R.L., Danishefsky S.J. On the direct epoxidation of glycals: application of a reiterative strategy for the synthesis of β-linked oligosaccharides. J. Am. Chem. Soc. 111:1989;6661-6666
    • (1989) J. Am. Chem. Soc. , vol.111 , pp. 6661-6666
    • Halcomb, R.L.1    Danishefsky, S.J.2
  • 187
    • 0001207175 scopus 로고    scopus 로고
    • Solid support oligosaccharide synthesis: Construction of β-linked oligosaccharides by coupling of glycal derived thioethyl glycosyl donors
    • Zheng C., Seeberger P.C., Danishefsky S.J. Solid support oligosaccharide synthesis: construction of β-linked oligosaccharides by coupling of glycal derived thioethyl glycosyl donors. J. Org. Chem. 63:1998;1126-1130
    • (1998) J. Org. Chem. , vol.63 , pp. 1126-1130
    • Zheng, C.1    Seeberger, P.C.2    Danishefsky, S.J.3
  • 188
    • 0021770863 scopus 로고
    • Synthesis of a glucoheptaose and a glucooctaose that elicit phytoalexin accumulation in soybean
    • Ossowski P., Pilotti Å., Garegg P.J., Lindberg B. Synthesis of a glucoheptaose and a glucooctaose that elicit phytoalexin accumulation in soybean. J. Biol. Chem. 259:1984;11337-11340
    • (1984) J. Biol. Chem. , vol.259 , pp. 11337-11340
    • Ossowski, P.1    Pilotti, Å.2    Garegg, P.J.3    Lindberg, B.4
  • 189
    • 0026102660 scopus 로고
    • Structure-activity relationships of oligo-β-glucoside elicitors of phytoalexin accumulation
    • and references therein
    • Birberg W., Cheong J.-J., Fügedi P., Pilotti Å., Garegg P.J., Hong N., Ogawa T., Hahn M.G. Structure-activity relationships of oligo-β-glucoside elicitors of phytoalexin accumulation. The Plant Cell. 3:1991;127-136. and references therein
    • (1991) The Plant Cell , vol.3 , pp. 127-136
    • Birberg, W.1    Cheong, J.-J.2    Fügedi, P.3    Pilotti, Å.4    Garegg, P.J.5    Hong, N.6    Ogawa, T.7    Hahn, M.G.8
  • 191
    • 84989547956 scopus 로고
    • Synthesis of a methyl heptaglucoside with phytoalexin elicitor activity based on oxidative coupling of glucals
    • Timmers C.M., van der Marel G.A., van Boom J.H. Synthesis of a methyl heptaglucoside with phytoalexin elicitor activity based on oxidative coupling of glucals. Eur. J. Chem. 1:1995;161-164
    • (1995) Eur. J. Chem. , vol.1 , pp. 161-164
    • Timmers, C.M.1    Van Der Marel, G.A.2    Van Boom, J.H.3
  • 192
    • 0001177442 scopus 로고
    • Synthesis of a branched heptasaccharide having phytoalexin-elicitor activity
    • Birberg W., Fügedi P., Garegg P.J., Pilotti Å. Synthesis of a branched heptasaccharide having phytoalexin-elicitor activity. Carbohydr. Res. 164:1987;297-312
    • (1987) Carbohydr. Res. , vol.164 , pp. 297-312
    • Birberg, W.1    Fügedi, P.2    Garegg, P.J.3    Pilotti, Å.4
  • 194
    • 0031048191 scopus 로고    scopus 로고
    • A general and highly efficient solid phase synthesis of oligosaccharides. Total synthesis of a heptasaccharide phytoalexin elicitor
    • Nicolaou K.C., Winsinger N., Pastor J., DeRoose F. A general and highly efficient solid phase synthesis of oligosaccharides. Total synthesis of a heptasaccharide phytoalexin elicitor. J. Am. Chem. Soc. 119:1997;449-450
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 449-450
    • Nicolaou, K.C.1    Winsinger, N.2    Pastor, J.3    Deroose, F.4
  • 195
  • 196
    • 0035936861 scopus 로고    scopus 로고
    • Automated solid-phase synthesis of oligosaccharides
    • Plante O.J., Palmacci E.R., Seeberger P.H. Automated solid-phase synthesis of oligosaccharides. Science. 291:2001;1523-1527
    • (2001) Science , vol.291 , pp. 1523-1527
    • Plante, O.J.1    Palmacci, E.R.2    Seeberger, P.H.3
  • 197
    • 0003120633 scopus 로고
    • The significance of certain numerical relations in the sugar group
    • Hudson C.S. The significance of certain numerical relations in the sugar
    • (1909) J. Am. Chem. Soc. , vol.31 , pp. 66-86
    • Hudson, C.S.1
  • 198
    • 0001976173 scopus 로고
    • Optical rotation and geometrical structure
    • D. H. Whiffen, Optical rotation and geometrical structure, Chem. Ind., (London), (1956) 964-968.
    • (1956) Chem. Ind. (London) , pp. 964-968
    • Whiffen, D.H.1
  • 199
    • 0442266571 scopus 로고
    • A useful model of optical activity. II. Optical activity of saturated cyclic compounds
    • Brewster J.H. A useful model of optical activity. II. Optical activity of saturated cyclic compounds. J. Am. Chem. Soc. 81:1959;5483-5493
    • (1959) J. Am. Chem. Soc. , vol.81 , pp. 5483-5493
    • Brewster, J.H.1
  • 200
    • 0001510557 scopus 로고
    • Applications of empirical rules for optical rotation to problems of conformational analysis
    • Lemieux R.U., Martin J.C. Applications of empirical rules for optical rotation to problems of conformational analysis. Carbohydr. Res. 13:1970;139-161
    • (1970) Carbohydr. Res. , vol.13 , pp. 139-161
    • Lemieux, R.U.1    Martin, J.C.2
  • 201
    • 11144320209 scopus 로고
    • Circular dichroism of 2-O-acetyl-3,6-dideoxy-D-xylohexopyranosides and of Salmonella typhimurium lipopolysaccharides
    • Garegg P.J., Borén H.B., Svensson S. Circular dichroism of 2-O-acetyl-3,6-dideoxy-D-xylohexopyranosides and of Salmonella typhimurium lipopolysaccharides. Acta Chem. Scand. 24:1970;3084-3086
    • (1970) Acta Chem. Scand. , vol.24 , pp. 3084-3086
    • Garegg, P.J.1    Borén, H.B.2    Svensson, S.3
  • 202
    • 0000541455 scopus 로고
    • Enzymic methods for the structure analysis of the carbohydrate chain of glycoproteins
    • Li Y.-T., Li S.-C. Enzymic methods for the structure analysis of the carbohydrate chain of glycoproteins. Methods Carbohydr. Chem. 7:1976;221-232
    • (1976) Methods Carbohydr. Chem. , vol.7 , pp. 221-232
    • Li, Y.-T.1    Li, S.-C.2
  • 203
    • 0000901642 scopus 로고
    • Configurational effects in the proton magnetic resonance spectra of acetylated carbohydrates
    • Lemieux R.U., Kullnig R.K., Bernstein H.J., Schneider W.G. Configurational effects in the proton magnetic resonance spectra of acetylated carbohydrates. J. Am. Chem. Soc. 79:1957;1005-1006
    • (1957) J. Am. Chem. Soc. , vol.79 , pp. 1005-1006
    • Lemieux, R.U.1    Kullnig, R.K.2    Bernstein, H.J.3    Schneider, W.G.4
  • 204
    • 0001588163 scopus 로고
    • Configuration effects on the proton magnetic resonance spectra of six-membered ring compounds
    • Lemieux R.U., Kullnig R.K., Bernstein H.J., Schneider W.G. Configuration effects on the proton magnetic resonance spectra of six-membered ring compounds. J. Am. Chem. Soc. 80:1958;6098-6105
    • (1958) J. Am. Chem. Soc. , vol.80 , pp. 6098-6105
    • Lemieux, R.U.1    Kullnig, R.K.2    Bernstein, H.J.3    Schneider, W.G.4
  • 206
    • 0034508404 scopus 로고    scopus 로고
    • Carbohydrate structural determination by NMR spectroscopy: Modern methods and limitations
    • This review has extensive tabulations of reviews related to NMR of carbohydrates, characteristic NMR features, and chemical shift collections in addition to 355 references.
    • J. Ø. Duus, C. H. Gottfredsen, and K. Bock, Carbohydrate structural determination by NMR spectroscopy: modern methods and limitations, Chem. Rev., (2000) 4589-4614. This review has extensive tabulations of reviews related to NMR of carbohydrates, characteristic NMR features, and chemical shift collections in addition to 355 references.
    • (2000) Chem. Rev. , pp. 4589-4614
    • Duus, J.Ø.1    Gottfredsen, C.H.2    Bock, K.3
  • 207
    • 49349137129 scopus 로고
    • The problem of conformational effects
    • Zefirov N.S. The problem of conformational effects. Tetrahedron. 33:1977;3193-3202
    • (1977) Tetrahedron , vol.33 , pp. 3193-3202
    • Zefirov, N.S.1
  • 208
    • 0002965416 scopus 로고
    • Stability of glycosides to acid hydrolysis
    • J. T. Edward, Stability of glycosides to acid hydrolysis, Chem. Ind., (1955) 1102-1104.
    • (1955) Chem. Ind. , pp. 1102-1104
    • Edward, J.T.1
  • 209
    • 4243938377 scopus 로고
    • Conformational and relative stabilities of acetylated sugars as determined by nuclear magnetic resonance
    • Lemieux R.U., Chü N.J. Conformational and relative stabilities of acetylated sugars as determined by nuclear magnetic resonance. Abstr. Pap. Am. Chem. Soc. Meet. 133:1964;31N
    • (1964) Abstr. Pap. Am. Chem. Soc. Meet. , vol.133
    • Lemieux, R.U.1    Chü, N.J.2
  • 210
    • 0011391244 scopus 로고
    • Conformational and chemical consequences of vicinal polar bonds
    • L. Phillips and V. Vray, Conformational and chemical consequences of vicinal polar bonds, J. Chem. Soc. Chem. Commun., (1973) 90-91.
    • (1973) J. Chem. Soc. Chem. Commun. , pp. 90-91
    • Phillips, L.1    Vray, V.2
  • 211
    • 33947091734 scopus 로고
    • Stereochemical consequences of adjacent electron pairs and polar bonds
    • Wolfe S. Stereochemical consequences of adjacent electron pairs and polar bonds. Acc. Chem. Res. 5:1972;102-111
    • (1972) Acc. Chem. Res. , vol.5 , pp. 102-111
    • Wolfe, S.1
  • 213
    • 0001339474 scopus 로고
    • Solvation effects on conformational equilibria. Studies related to the conformational properties of 2-methoxytetrahydropyran an related methyl glycopyranosides
    • Lemieux R.U., Pavia A.A., Martin J.C., Watabe K.A. Solvation effects on conformational equilibria. Studies related to the conformational properties of 2-methoxytetrahydropyran an related methyl glycopyranosides. Can. J. Chem. 47:1969;4427-4439
    • (1969) Can. J. Chem. , vol.47 , pp. 4427-4439
    • Lemieux, R.U.1    Pavia, A.A.2    Martin, J.C.3    Watabe, K.A.4
  • 214
    • 0000744455 scopus 로고
    • The abnormal conformation of pyridinium α-glucopyranosides
    • Lemieux R.U., Morgan A.R. The abnormal conformation of pyridinium α-glucopyranosides. Can. J. Chem. 43:1965;2205-2213
    • (1965) Can. J. Chem. , vol.43 , pp. 2205-2213
    • Lemieux, R.U.1    Morgan, A.R.2
  • 215
    • 0033612757 scopus 로고    scopus 로고
    • Absence of reverse anomeric effect in glycosylimidazoles
    • and references therein
    • Charles L., Fabian M.A., Brunckova J., K Ohta B. Absence of reverse anomeric effect in glycosylimidazoles. J. Am. Chem. Soc. 121:1999;6811-6918. and references therein
    • (1999) J. Am. Chem. Soc. , vol.121 , pp. 6811-6918
    • Charles, L.1    Fabian, M.A.2    Brunckova, J.3    Ohta, B.K.4
  • 216
    • 4243620067 scopus 로고
    • Mechanism in carbohydrate chemistry
    • Capon B. Mechanism in carbohydrate chemistry. Chem. Rev. 69:1969;407-496
    • (1969) Chem. Rev. , vol.69 , pp. 407-496
    • Capon, B.1
  • 217
    • 0033248867 scopus 로고    scopus 로고
    • Anomerization of methyl glycosides by acid-catalyzed methanolysis: Trapping of intermediates
    • Garegg P.J., Johansson K.-J., Konradsson P., Lindberg B. Anomerization of methyl glycosides by acid-catalyzed methanolysis: Trapping of intermediates. J. Carbohydr. Chem. 18:1999;31-40
    • (1999) J. Carbohydr. Chem. , vol.18 , pp. 31-40
    • Garegg, P.J.1    Johansson, K.-J.2    Konradsson, P.3    Lindberg, B.4
  • 218
    • 37049060779 scopus 로고
    • Mechanism of reaction in the sugar series. III. Acid-catalyzed hydrolysis of tert-butyl β-D-glucopyranoside and other glycosides
    • C. Armour, C. A. Bunton, S. Patai, L. H. Selman, and C. A. Vernon, Mechanism of reaction in the sugar series. III. Acid-catalyzed hydrolysis of tert-butyl β-D-glucopyranoside and other glycosides, J. Chem. Soc., (1961) 412-416.
    • (1961) J. Chem. Soc. , pp. 412-416
    • Armour, C.1    Bunton, C.A.2    Patai, S.3    Selman, L.H.4    Vernon, C.A.5
  • 219
    • 1542758656 scopus 로고    scopus 로고
    • Mechanism of hydrolysis of isopropenyl glycopyranosides. Spectroscopic evidence concerning the greater reactivity of the α-anomer
    • Chenault H.K., Chafin L.F. Mechanism of hydrolysis of isopropenyl glycopyranosides. Spectroscopic evidence concerning the greater reactivity of the α-anomer. J. Org. Chem. 63:1998;833-840
    • (1998) J. Org. Chem. , vol.63 , pp. 833-840
    • Chenault, H.K.1    Chafin, L.F.2
  • 220
    • 11144258483 scopus 로고
    • B. Capon. Reactions at high pressure. Part 8. The mechanism af acid-catalysed hydrolyses of glycosides
    • Isaachs N.S., Javaid K. B. Capon. Reactions at high pressure. Part 8. The mechanism af acid-catalysed hydrolyses of glycosides. J. Chem. Soc. Perkin Trans. 2:1983;101-103
    • (1983) J. Chem. Soc. Perkin Trans. , vol.2 , pp. 101-103
    • Isaachs, N.S.1    Javaid, K.2
  • 221
    • 11144274224 scopus 로고
    • Kinetic evidence of anionic intermediates in the base-catalyzed cleavage of glycosidic bonds in methyl D-glucopyranosides
    • Lai Y.Z. Kinetic evidence of anionic intermediates in the base-catalyzed cleavage of glycosidic bonds in methyl D-glucopyranosides. Carbohyd. Res. 24:1972;57-65
    • (1972) Carbohyd. Res. , vol.24 , pp. 57-65
    • Lai, Y.Z.1
  • 222
    • 11144348494 scopus 로고
    • C-2 Oxyanion participation in the base-catalyzed cleavage of p-nitrophenyl β-D-galactopyranoside and p-nitrophenyl α-D- mannopyranoside
    • Gasman R.C., Johnson D.C. C-2 Oxyanion participation in the base-catalyzed cleavage of p-nitrophenyl β-D-galactopyranoside and p-nitrophenyl α-D-mannopyranoside. J. Org. Chem. 31:1966;1808-1830
    • (1966) J. Org. Chem. , vol.31 , pp. 1808-1830
    • Gasman, R.C.1    Johnson, D.C.2
  • 223
    • 37049123788 scopus 로고
    • Migration of the O-p-nitrophenyl group. Mechanism whereby p-nitrophenyl α-D-glycosides liberate p-nitrophenoxide in alkaline solution
    • D. Horton and A. E. Luetzow. Migration of the O-p-nitrophenyl group. Mechanism whereby p-nitrophenyl α-D-glycosides liberate p-nitrophenoxide in alkaline solution, J. C. S. Chem. Commun., (1971) 79-81.
    • (1971) J. C. S. Chem. Commun. , pp. 79-81
    • Horton, D.1    Luetzow, A.E.2
  • 225
    • 0019980770 scopus 로고
    • Reductive cleavage of glycosides
    • Rolf and G. R. Gray, Reductive cleavage of glycosides, J. Am. Chem. Soc., 104 (1982) 3539-3541.
    • (1982) J. Am. Chem. Soc. , vol.104 , pp. 3539-3541
    • Rolf1    Gray, G.R.2
  • 226
    • 11144327404 scopus 로고    scopus 로고
    • New technology for carbohydrate structural analysis
    • San Diego, CA (April 1-5).
    • G. R. Gray, New technology for carbohydrate structural analysis, Abstr. Carb. 24, 221st ACS National meeting, San Diego, CA (2001, April 1-5).
    • (2001) Abstr. Carb. 24, 221st ACS National Meeting
    • Gray, G.R.1
  • 227
    • 85178423449 scopus 로고
    • Zur Kentnis der Aceton-Zucker. XIII: Die hydrolyse einiger Disaccharide, Glucoside und Aceton-Zucker
    • K. Freudenberg, W. Dürr, and H. von Hochstetter, Zur Kentnis der Aceton-Zucker. XIII: Die hydrolyse einiger Disaccharide, Glucoside und Aceton-Zucker, Ber., 61 (1928) 1735-1743.
    • (1928) Ber. , vol.61 , pp. 1735-1743
    • Freudenberg, K.1    Dürr, W.2    Von Hochstetter, H.3
  • 228
  • 229
    • 0003133973 scopus 로고
    • Regioselective hydrogenolysis of benzyl glycosides
    • Bieg T., Szeja W. Regioselective hydrogenolysis of benzyl glycosides. Carbohydr. Res. 205:1990;C10-C11
    • (1990) Carbohydr. Res. , vol.205
    • Bieg, T.1    Szeja, W.2
  • 230
    • 33845278486 scopus 로고
    • 2-(Trimethylsilyl)ethyl) glycosides. Synthesis, anomeric deblocking and transformation into 1,2-trans-1-O-acyl sugars
    • and references therein
    • Jansson K., Ahlfors S., Frejd T., Kihlberg J., Magnusson G., Dahmen J., Noori G., Stenvall K. 2-(Trimethylsilyl)ethyl) glycosides. Synthesis, anomeric deblocking and transformation into 1,2-trans-1-O-acyl sugars. J. Org. Chem. 53:1988;5629-5647. and references therein
    • (1988) J. Org. Chem. , vol.53 , pp. 5629-5647
    • Jansson, K.1    Ahlfors, S.2    Frejd, T.3    Kihlberg, J.4    Magnusson, G.5    Dahmen, J.6    Noori, G.7    Stenvall, K.8
  • 231
    • 0009162720 scopus 로고
    • A glycosylation reaction: Conversion of glycosides to glycosyl chlorides by boron trichloride
    • and references therein
    • Perdomo G.R., Krepinsky J. A glycosylation reaction: Conversion of glycosides to glycosyl chlorides by boron trichloride. Tetrahedron Lett. 28:1987;5595-5598. and references therein
    • (1987) Tetrahedron Lett. , vol.28 , pp. 5595-5598
    • Perdomo, G.R.1    Krepinsky, J.2
  • 232
    • 0025358881 scopus 로고
    • A facile, one-step procedure for the conversion of 2-trimethylsilyl)ethyl glycosides to their glycosyl chlorides
    • Ravindranathan K., Kartha P., Jennings H.J. A facile, one-step procedure for the conversion of 2-trimethylsilyl)ethyl glycosides to their glycosyl chlorides. Tetrahedron Lett. 31:1990;2537-2540
    • (1990) Tetrahedron Lett. , vol.31 , pp. 2537-2540
    • Ravindranathan, K.1    Kartha, P.2    Jennings, H.J.3
  • 233
    • 0025277564 scopus 로고
    • 2-(Trimethylsilyl)ethyl glycosides. Transformation into glycopyranosyl chlorides
    • Jansson K., Noori G., Magnusson G. 2-(Trimethylsilyl)ethyl glycosides. Transformation into glycopyranosyl chlorides. J. Org. Chem. 55:1990;3181-3185
    • (1990) J. Org. Chem. , vol.55 , pp. 3181-3185
    • Jansson, K.1    Noori, G.2    Magnusson, G.3
  • 234
    • 84987573989 scopus 로고
    • Glycosylidene carbenes. Part 6. Synthesis of alkyl and fluoroalkyl glycosides
    • Briner K., Vasella A. Glycosylidene carbenes. Part 6. Synthesis of alkyl and fluoroalkyl glycosides. Helv. Chim. Acta. 75:1992;621-625
    • (1992) Helv. Chim. Acta , vol.75 , pp. 621-625
    • Briner, K.1    Vasella, A.2
  • 235
    • 0011217897 scopus 로고    scopus 로고
    • Activation of selenoglycosides by photoinduced electron transfer
    • T. Furuta, K. Takeuchi, and M. Iwamura, Activation of selenoglycosides by photoinduced electron transfer, Chem. Commun., (1996) 157-158.
    • (1996) Chem. Commun. , pp. 157-158
    • Furuta, T.1    Takeuchi, K.2    Iwamura, M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.