메뉴 건너뛰기




Volumn 3, Issue 2, 1997, Pages 75-94

Carbohydrate-based combinatorial libraries

Author keywords

Carbohydrates; Combinatorial; Glycoconjugates; Libraries; Solid phase; Solution phase

Indexed keywords

BAUHINIA PURPUREA LECTIN; CARBOHYDRATE; GLYCOCONJUGATE; GLYCOPEPTIDE; LECTIN; OLIGOSACCHARIDE; PEPTIDOGLYCAN; PLANT LECTIN; POLYSTYRENE DERIVATIVE; TENTAGEL RESIN;

EID: 0031994805     PISSN: 13811991     EISSN: None     Source Type: Journal    
DOI: 10.1023/a:1009650424835     Document Type: Article
Times cited : (66)

References (80)
  • 1
    • 0028243847 scopus 로고
    • Applications of combinatorial technologies to drug discovery. 1. Background and peptide combinatorial libraries
    • Gallop, M.A., Barrett, R.W., Dower, W.J., Fodor, S.P.A. and Gordon, E.M., Applications of combinatorial technologies to drug discovery. 1. Background and peptide combinatorial libraries, J. Med. Chem., 37 (1994) 1233-1251.
    • (1994) J. Med. Chem. , vol.37 , pp. 1233-1251
    • Gallop, M.A.1    Barrett, R.W.2    Dower, W.J.3    Fodor, S.P.A.4    Gordon, E.M.5
  • 2
    • 0028318863 scopus 로고
    • Applications of combinatorial technologies to drug discovery. 2. Combinatorial organic synthesis, library screening strategies and future directions
    • Gordon, E.M., Barrett, R.W., Dower, W.J., Fodor, S.P.A. and Gallop, M.A., Applications of combinatorial technologies to drug discovery. 2. Combinatorial organic synthesis, library screening strategies and future directions, J. Med. Chem., 37 (1994) 1385-1400.
    • (1994) J. Med. Chem. , vol.37 , pp. 1385-1400
    • Gordon, E.M.1    Barrett, R.W.2    Dower, W.J.3    Fodor, S.P.A.4    Gallop, M.A.5
  • 3
    • 0027318961 scopus 로고
    • Biological roles of oligosaccharides: All of the theories are correct
    • Varki, A., Biological roles of oligosaccharides: All of the theories are correct, Glycobiology, 3 (1993) 97-130.
    • (1993) Glycobiology , vol.3 , pp. 97-130
    • Varki, A.1
  • 5
    • 0009998435 scopus 로고
    • Drugs based on carbohydrates: Past and future
    • Kovac, P. (Ed.) Synthetic Oligosaccharides Indispensible Probes for the Life Sciences, American Chemical Society, Washington, DC
    • Petitou, M., Drugs based on carbohydrates: Past and future, In Kovac, P. (Ed.) Synthetic Oligosaccharides Indispensible Probes for the Life Sciences, ACS Symposium Series 560, American Chemical Society, Washington, DC, 1994, pp. 19-50.
    • (1994) ACS Symposium Series 560 , pp. 19-50
    • Petitou, M.1
  • 9
    • 0003012148 scopus 로고    scopus 로고
    • How water provides the impetus for molecular recognition in aqueous solution
    • Lemieux, R.U., How water provides the impetus for molecular recognition in aqueous solution, Acc. Chem. Res., 29 (1996) 373-380.
    • (1996) Acc. Chem. Res. , vol.29 , pp. 373-380
    • Lemieux, R.U.1
  • 10
    • 0028117752 scopus 로고
    • Tagged versus untagged libraries: Methods for the generation and screening of combinatorial chemical libraries
    • Janda, K.D., Tagged versus untagged libraries: Methods for the generation and screening of combinatorial chemical libraries, Proc. Natl. Acad. Sci. USA, 91 (1994) 10779-10785.
    • (1994) Proc. Natl. Acad. Sci. USA , vol.91 , pp. 10779-10785
    • Janda, K.D.1
  • 11
    • 7044263277 scopus 로고    scopus 로고
    • Synthesis and applications of small-molecule libraries
    • Thompson, L.A. and Ellman, J.A., Synthesis and applications of small-molecule libraries, Chem. Rev., 96 (1996) 555-600.
    • (1996) Chem. Rev. , vol.96 , pp. 555-600
    • Thompson, L.A.1    Ellman, J.A.2
  • 13
    • 33947291827 scopus 로고
    • Solid-phase synthesis of oligosaccharides. I. Preparation of the solid support. Poly[p-(1-propen-3-ol-1-yl)styrene]
    • Frechet, J.M. and Schuerch, C., Solid-phase synthesis of oligosaccharides. I. Preparation of the solid support. Poly[p-(1-propen-3-ol-1-yl)styrene], J. Am. Chem. Soc., 93 (1971) 492-496.
    • (1971) J. Am. Chem. Soc. , vol.93 , pp. 492-496
    • Frechet, J.M.1    Schuerch, C.2
  • 14
    • 33748519998 scopus 로고
    • Solid-phase synthesis of oligosaccharides III. Preparation of some derivatives of di-and tri-saccharides via a simple alcoholysis reaction
    • Frechet, J.M. and Schuerch, C., Solid-phase synthesis of oligosaccharides III. Preparation of some derivatives of di-and tri-saccharides via a simple alcoholysis reaction, Carbohydr. Res., 22 (1972) 399-412.
    • (1972) Carbohydr. Res. , vol.22 , pp. 399-412
    • Frechet, J.M.1    Schuerch, C.2
  • 15
    • 33745113184 scopus 로고
    • Solid-phase synthesis of oligosaccharides. II. Steric control by C-6 substituents in glucoside synthesis
    • Frechet, J.M. and Schuerch, C., Solid-phase synthesis of oligosaccharides. II. Steric control by C-6 substituents in glucoside synthesis, J. Am. Chem. Soc., 94 (1972) 604-609.
    • (1972) J. Am. Chem. Soc. , vol.94 , pp. 604-609
    • Frechet, J.M.1    Schuerch, C.2
  • 16
    • 0000659413 scopus 로고
    • Light-sensitive glycosides. I. 6-Nitroveratryl β-D-glucopyranoside and 2-nitrobenzyl β-D-glucopyranoside
    • Zehavi, U., Amit, B. and Patchornik, A., Light-sensitive glycosides. I. 6-Nitroveratryl β-D-glucopyranoside and 2-nitrobenzyl β-D-glucopyranoside, J. Org. Chem., 37 (1972) 2281-2284.
    • (1972) J. Org. Chem. , vol.37 , pp. 2281-2284
    • Zehavi, U.1    Amit, B.2    Patchornik, A.3
  • 17
    • 0015932858 scopus 로고
    • Oligosaccharide synthesis on a light-sensitive solid support. I. The polymer and synthesis of isomaltose (6-O-α-D-glucopyranosyl-D-glucose)
    • Zehavi, U. and Patchornik, A., Oligosaccharide synthesis on a light-sensitive solid support. I. The polymer and synthesis of isomaltose (6-O-α-D-glucopyranosyl-D-glucose), J. Am. Chem. Soc., 95 (1973) 5673-5677.
    • (1973) J. Am. Chem. Soc. , vol.95 , pp. 5673-5677
    • Zehavi, U.1    Patchornik, A.2
  • 18
    • 0000750401 scopus 로고
    • Light-sensitive glycosides. II. 2-Nitrobenzyl 6-deoxy-α-L-mannopyranoside and 2-nitrobenzyl 6-deoxy-β-galactopyranoside
    • Zehavi, U. and Patchornik, A., Light-sensitive glycosides. II. 2-Nitrobenzyl 6-deoxy-α-L-mannopyranoside and 2-nitrobenzyl 6-deoxy-β-galactopyranoside, J. Org. Chem., 37 (1972) 2285-2288.
    • (1972) J. Org. Chem. , vol.37 , pp. 2285-2288
    • Zehavi, U.1    Patchornik, A.2
  • 19
    • 37049133555 scopus 로고
    • Synthesis of oligosaccharides on polymer supports. Part I. 6-O-(p-vinylbenzoyl) derivatives of glucopyranose and their copolymers with styrene
    • Guthrie, R.D., Jenkins, A.D. and Stehlicek, J., Synthesis of oligosaccharides on polymer supports. Part I. 6-O-(p-vinylbenzoyl) derivatives of glucopyranose and their copolymers with styrene, J. Chem. Soc. C. (1971) 2690-2696.
    • (1971) J. Chem. Soc. C , pp. 2690-2696
    • Guthrie, R.D.1    Jenkins, A.D.2    Stehlicek, J.3
  • 20
    • 37049126781 scopus 로고
    • Synthesis of oligosaccharides on polymer supports. Part II. Synthesis of β-D-gentiobiose derivatives on soluble support copolymers of styrene and 6-O-(p-vinylbenzoyl) or 6-O-(p-vinylphenylsulphonyl) derivatives of D-glucopyranose
    • Guthrie, R.D., Jenkins, A.D. and Roberts, G.A.F., Synthesis of oligosaccharides on polymer supports. Part II. Synthesis of β-D-gentiobiose derivatives on soluble support copolymers of styrene and 6-O-(p-vinylbenzoyl) or 6-O-(p-vinylphenylsulphonyl) derivatives of D-glucopyranose, J. Chem. Soc. Perkin Trans. 1, (1973) 2414-2417.
    • (1973) J. Chem. Soc. Perkin Trans. 1 , pp. 2414-2417
    • Guthrie, R.D.1    Jenkins, A.D.2    Roberts, G.A.F.3
  • 21
    • 0001918767 scopus 로고
    • Solid-phase synthesis of oligosaccharides. II. Synthesis of 2-acetamindo-6-O-(2-acetamindo-2-deoxy-β-D-glucopyranosyl)-2-deoxy-D- glucose
    • Excoffier, G., Gagnaire, D., Utille, J.P. and Vignon, M., Solid-phase synthesis of oligosaccharides. II. Synthesis of 2-acetamindo-6-O-(2-acetamindo-2-deoxy-β-D-glucopyranosyl)-2-deoxy-D- glucose, Tetrahedron Lett. (1972) 5065-5068.
    • (1972) Tetrahedron Lett. , pp. 5065-5068
    • Excoffier, G.1    Gagnaire, D.2    Utille, J.P.3    Vignon, M.4
  • 23
    • 0000508254 scopus 로고
    • Glycosylation on the Merrifield resin using anomeric sulfoxides
    • Yan, L., Taylor, C.M., Goodnow Jr., R. and 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
  • 24
    • 0003176166 scopus 로고
    • A new base-labile anchoring group for polymer-supported oligosaccharide synthesis
    • Wang, Y., Zhang, H. and Voelter, W., A new base-labile anchoring group for polymer-supported oligosaccharide synthesis, Chem. Lett. (1995) 273-274.
    • (1995) Chem. Lett. , pp. 273-274
    • Wang, Y.1    Zhang, H.2    Voelter, W.3
  • 25
    • 0027591808 scopus 로고
    • A strategy for the solid-phase synthesis of oligosaccharides
    • Danishefsky, S.J., McClure, K.F., Randolph, J.T. and Ruggeri, R.B., A strategy for the solid-phase synthesis of oligosaccharides, Science, 260 (1993) 1307-1309.
    • (1993) Science , vol.260 , pp. 1307-1309
    • Danishefsky, S.J.1    McClure, K.F.2    Randolph, J.T.3    Ruggeri, R.B.4
  • 27
    • 0029007777 scopus 로고
    • Major simplifications in oligosaccharide syntheses arising from a solid-phase based method: An application to the synthesis of the Lewis b antigen
    • Randolph, J.T., McClure, K.F. and Danishefsky, S.J., Major simplifications in oligosaccharide syntheses arising from a solid-phase based method: An application to the synthesis of the Lewis b antigen, J. Am. Chem. Soc., 117 (1995) 5712-5719.
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 5712-5719
    • Randolph, J.T.1    McClure, K.F.2    Danishefsky, S.J.3
  • 28
    • 0001686537 scopus 로고
    • Polymer-supported solution synthesis of oligosaccharides
    • Douglas, S.P., Whitfield, D.M. and Krepinsky, J.J., Polymer-supported solution synthesis of oligosaccharides, J. Am. Chem. Soc., 113 (1991) 5095-5097.
    • (1991) J. Am. Chem. Soc. , vol.113 , pp. 5095-5097
    • Douglas, S.P.1    Whitfield, D.M.2    Krepinsky, J.J.3
  • 29
    • 0028886622 scopus 로고
    • Polymer-supported solution synthesis of oligosaccharides using a novel versatile linker for the synthesis of D-mannopentaose, a structural unit of D-mannans of pathogenic yeasts
    • Douglas, S.P., Whitfield, D.M. and Krepinsky, J.J., Polymer-supported solution synthesis of oligosaccharides using a novel versatile linker for the synthesis of D-mannopentaose, a structural unit of D-mannans of pathogenic yeasts, J. Am. Chem. Soc., 117 (1995) 2116-2117.
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 2116-2117
    • Douglas, S.P.1    Whitfield, D.M.2    Krepinsky, J.J.3
  • 30
    • 0000653311 scopus 로고
    • Syntheses of model oligosaccharides of biological significance. XIII. Syntheses of derivatives of GalpNAc(β 1-4)Galp(β 1-O), the common binding theme of adhesins of various bacteria: Solution and polymer-supported solution approaches. An improved preparation of 2-deoxy-2-phthalimido-1,3,4,6-tetra-O-acetyl galactosamine and glucosamine
    • Leung, O.-T., Douglas, S.P., Whitfield, D.M., Pang, H.Y.S. and Krepinsky, J.J., Syntheses of model oligosaccharides of biological significance. XIII. Syntheses of derivatives of GalpNAc(β 1-4)Galp(β 1-O), the common binding theme of adhesins of various bacteria: Solution and polymer-supported solution approaches. An improved preparation of 2-deoxy-2-phthalimido-1,3,4,6-tetra-O-acetyl galactosamine and glucosamine, New J. Chem., 18 (1994) 349-363.
    • (1994) New J. Chem. , vol.18 , pp. 349-363
    • Leung, O.-T.1    Douglas, S.P.2    Whitfield, D.M.3    Pang, H.Y.S.4    Krepinsky, J.J.5
  • 31
    • 0031048191 scopus 로고    scopus 로고
    • A general and highly efficient solid phase synthesis of oligosaccharides. Total synthesis of a heptasaccharide phytoalexin elicitor (HPE)
    • Nicolaou, K.C., Winssinger, N., Pastor, J. and DeRoose, F., A general and highly efficient solid phase synthesis of oligosaccharides. Total synthesis of a heptasaccharide phytoalexin elicitor (HPE), J. Am. Chem. Soc., 119 (1997) 449-450.
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 449-450
    • Nicolaou, K.C.1    Winssinger, N.2    Pastor, J.3    DeRoose, F.4
  • 32
    • 0002081061 scopus 로고    scopus 로고
    • Use of low molecular weight polyethylene glycol linker for polymer-supported solution synthesis of oligosaccharides
    • Jiang, L., Hartley, R.C. and Chan, T.-H., Use of low molecular weight polyethylene glycol linker for polymer-supported solution synthesis of oligosaccharides, Chem. Commun. (1996) 2193-2194.
    • (1996) Chem. Commun. , pp. 2193-2194
    • Jiang, L.1    Hartley, R.C.2    Chan, T.-H.3
  • 33
    • 0028587090 scopus 로고
    • Solution and solid-phase synthesis of inhibitors of H. pylori attachment and E-selectin-mediated leukocyte adhesion
    • Halcomb, R.L., Huang, H. and Wong, C.-H., Solution and solid-phase synthesis of inhibitors of H. pylori attachment and E-selectin-mediated leukocyte adhesion, J. Am. Chem. Soc., 116 (1994) 11315-11322.
    • (1994) J. Am. Chem. Soc. , vol.116 , pp. 11315-11322
    • Halcomb, R.L.1    Huang, H.2    Wong, C.-H.3
  • 34
    • 0029163690 scopus 로고
    • Enzymes in organic synthesis: Application to the problems of carbohydrate recognition (part 2)
    • Wong, C.-H., Halcomb, R.L., Ichikawa, Y. and Kajimoto, T., Enzymes in organic synthesis: Application to the problems of carbohydrate recognition (part 2), 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
  • 37
  • 39
    • 0029872650 scopus 로고    scopus 로고
    • Synthesis of a new carbohydrate mimetic: 'Carbopeptoid' containing a C-1 carboxylate and C-2 amino group
    • Suhara, Y., Hildreth, J.E.K. and Ichikawa, Y., Synthesis of a new carbohydrate mimetic: 'Carbopeptoid' containing a C-1 carboxylate and C-2 amino group, Tetrahedron Lett., 37 (1996) 1575-1578.
    • (1996) Tetrahedron Lett. , vol.37 , pp. 1575-1578
    • Suhara, Y.1    Hildreth, J.E.K.2    Ichikawa, Y.3
  • 41
    • 0028790946 scopus 로고
    • Synthesis and biological activity of oligosaccharide libraries
    • Alavi, A. and Axford, J.S. (Eds.) Plenum, New York, NY
    • Ding, Y., Kanie, O., Labbe, J., Palcic, M.M., Ernst, B. and Hindsgaul, O., Synthesis and biological activity of oligosaccharide libraries, In Alavi, A. and Axford, J.S. (Eds.) Glycoimmunology, Plenum, New York, NY, 1995, pp. 261-269.
    • (1995) Glycoimmunology , pp. 261-269
    • Ding, Y.1    Kanie, O.2    Labbe, J.3    Palcic, M.M.4    Ernst, B.5    Hindsgaul, O.6
  • 42
    • 0001845514 scopus 로고    scopus 로고
    • Generation of oligosaccharide and glycoconjugate libraries for drug discovery
    • Sofia, M.J., Generation of oligosaccharide and glycoconjugate libraries for drug discovery, Drug Discov. Today, 1 (1996) 27-34.
    • (1996) Drug Discov. Today , vol.1 , pp. 27-34
    • Sofia, M.J.1
  • 43
    • 0028032234 scopus 로고
    • Recent developments in glycopeptide and oligosaccharide synthesis
    • Meldal, M., Recent developments in glycopeptide and oligosaccharide synthesis, Curr. Opin. Struct. Biol., 4 (1994) 710-718.
    • (1994) Curr. Opin. Struct. Biol. , vol.4 , pp. 710-718
    • Meldal, M.1
  • 44
    • 0028041060 scopus 로고
    • A general approach to the synthesis of O- and N-linked glycopeptides
    • Meldal, M. and Bock, K., A general approach to the synthesis of O- and N-linked glycopeptides, Glycoconjugate J., 11 (1994) 59-63.
    • (1994) Glycoconjugate J. , vol.11 , pp. 59-63
    • Meldal, M.1    Bock, K.2
  • 45
    • 0027360551 scopus 로고
    • Synthesis of oligosaccharides, glycoconjugates, and glycolipids
    • Halcomb, R.L. and Wong, C.-H., Synthesis of oligosaccharides, glycoconjugates, and glycolipids, Curr. Opin. Struct. Biol., 3 (1993) 694-700.
    • (1993) Curr. Opin. Struct. Biol. , vol.3 , pp. 694-700
    • Halcomb, R.L.1    Wong, C.-H.2
  • 46
    • 0027249312 scopus 로고
    • Solid-phase synthesis of O-mannosylated peptides: Two strategies compared
    • Andrews, D.M. and Seale, P.W., Solid-phase synthesis of O-mannosylated peptides: Two strategies compared, Int. J. Pept. Protein Res., 42 (1993) 165-170.
    • (1993) Int. J. Pept. Protein Res. , vol.42 , pp. 165-170
    • Andrews, D.M.1    Seale, P.W.2
  • 47
    • 0027951227 scopus 로고
    • Solid-phase chemical-enzymatic synthesis of glycopeptides and oligosaccharides
    • Schuster, M., Wang, P., Paulson, J.C. and Wong, C.-H., Solid-phase chemical-enzymatic synthesis of glycopeptides and oligosaccharides, J. Am. Chem. Soc., 116 (1994) 1135-1136.
    • (1994) J. Am. Chem. Soc. , vol.116 , pp. 1135-1136
    • Schuster, M.1    Wang, P.2    Paulson, J.C.3    Wong, C.-H.4
  • 48
    • 0026092642 scopus 로고
    • Solid-phase synthesis of glycopeptides: Glycosylation of resin-bound serine-peptides by 3,4,6-tri-O-acetyl-D-glucose-oxazoline
    • Hollosi, M., Kollat, E., Laczko, I., Medzihradszky, K.F., Thurin, J. and Otvos Jr., L., Solid-phase synthesis of glycopeptides: Glycosylation of resin-bound serine-peptides by 3,4,6-tri-O-acetyl-D-glucose-oxazoline, Tetrahedron Lett., 32 (1991) 1531-1534.
    • (1991) Tetrahedron Lett. , vol.32 , pp. 1531-1534
    • Hollosi, M.1    Kollat, E.2    Laczko, I.3    Medzihradszky, K.F.4    Thurin, J.5    Otvos Jr., L.6
  • 49
    • 0001270462 scopus 로고
    • A practical, convergent method for glycopeptide synthesis
    • Cohen-Anisfeld, S.T. and Lansbury Jr., P.T., A practical, convergent method for glycopeptide synthesis, J. Am. Chem. Soc., 115 (1993) 10531-10537.
    • (1993) J. Am. Chem. Soc. , vol.115 , pp. 10531-10537
    • Cohen-Anisfeld, S.T.1    Lansbury Jr., P.T.2
  • 50
    • 0029049463 scopus 로고
    • A strategy for a convergent synthesis of N-linked glycopeptides on a solid support
    • Roberge, J.Y., Beebe, X. and Danishefsky, S.J., A strategy for a convergent synthesis of N-linked glycopeptides on a solid support, Science, 269 (1995) 202-204.
    • (1995) Science , vol.269 , pp. 202-204
    • Roberge, J.Y.1    Beebe, X.2    Danishefsky, S.J.3
  • 51
    • 0029302620 scopus 로고
    • Strategies for the synthesis and screening of glycoconjugates. 1. A library of glycosylamines
    • Vetter, D. and Gallop, M.A., Strategies for the synthesis and screening of glycoconjugates. 1. A library of glycosylamines, Bioconjugate Chem., 6 (1995) 316-318.
    • (1995) Bioconjugate Chem. , vol.6 , pp. 316-318
    • Vetter, D.1    Gallop, M.A.2
  • 53
    • 0029298987 scopus 로고
    • Strategies for the synthesis and screening of glycoconjugates. 2. Covalent immobilization for flow cytometry
    • Vetter, D., Tate, E.M. and Gallop, M.A., Strategies for the synthesis and screening of glycoconjugates. 2. Covalent immobilization for flow cytometry, Bioconjugate Chem., 6 (1995) 319-322.
    • (1995) Bioconjugate Chem. , vol.6 , pp. 319-322
    • Vetter, D.1    Tate, E.M.2    Gallop, M.A.3
  • 54
    • 0030569319 scopus 로고    scopus 로고
    • Solid phase synthesis of peptidoglycan monomers for the generation of a combinatorial library
    • Chan, T.Y., Chen, A., Allanson, N., Chen, R., Liu, D. and Sofia, M.J., Solid phase synthesis of peptidoglycan monomers for the generation of a combinatorial library, Tetrahedron Lett., 37 (1996) 8097-8100.
    • (1996) Tetrahedron Lett. , vol.37 , pp. 8097-8100
    • Chan, T.Y.1    Chen, A.2    Allanson, N.3    Chen, R.4    Liu, D.5    Sofia, M.J.6
  • 56
    • 0025094571 scopus 로고
    • 3-α-D-Manp-1-]-threonine-O-Pfp as a building block in solid phase synthesis of an O-linked dimannosyl glycopeptide
    • 3-α-D-Manp-1-]-threonine-O-Pfp as a building block in solid phase synthesis of an O-linked dimannosyl glycopeptide, Tetrahedron Lett., 31 (1990) 6991-6994.
    • (1990) Tetrahedron Lett. , vol.31 , pp. 6991-6994
    • Jansson, A.M.1    Meldal, M.2    Bock, K.3
  • 57
    • 0025059755 scopus 로고
    • Pentafluorophenyl esters for temporary carboxyl group protection in solid phase synthesis of N-linked glycopeptides
    • Meldal, M. and Bock, K., Pentafluorophenyl esters for temporary carboxyl group protection in solid phase synthesis of N-linked glycopeptides, Tetrahedron Lett., 31 (1990) 6987-6990.
    • (1990) Tetrahedron Lett. , vol.31 , pp. 6987-6990
    • Meldal, M.1    Bock, K.2
  • 59
    • 37049067742 scopus 로고
    • Solid-phase synthesis and characterization of O-dimannosylated heptadecapeptide analogues of human insulin-like growth factor 1 (IGF-1)
    • Jansson, A.M., Meldal, M. and Bock, K., Solid-phase synthesis and characterization of O-dimannosylated heptadecapeptide analogues of human insulin-like growth factor 1 (IGF-1), J. Chem. Soc., Perkin Trans. 1, (1992) 1699-1707.
    • (1992) J. Chem. Soc., Perkin Trans. 1 , pp. 1699-1707
    • Jansson, A.M.1    Meldal, M.2    Bock, K.3
  • 60
    • 37049083309 scopus 로고
    • Small-scale solid-phase O-glycopeptide synthesis of linear and cyclized hexapeptides from blood-clotting factor IX containing O-(α-D-Xyl-1-3-α-D-Xyl-1-3-β-D-Glc)-L-Ser
    • Reimer, K.B., Meldal, M., Kusumoto, S., Fukase, K. and Bock, K., Small-scale solid-phase O-glycopeptide synthesis of linear and cyclized hexapeptides from blood-clotting factor IX containing O-(α-D-Xyl-1-3-α-D-Xyl-1-3-β-D-Glc)-L-Ser, J. Chem. Soc., Perkin Trans. 1, (1993) 925-932.
    • (1993) J. Chem. Soc., Perkin Trans. 1 , pp. 925-932
    • Reimer, K.B.1    Meldal, M.2    Kusumoto, S.3    Fukase, K.4    Bock, K.5
  • 61
    • 37049073528 scopus 로고
    • Synthesis of mannose 6-phosphate-containing disaccharide threonine building blocks and their use in solid-phase glycopeptide synthesis
    • Christensen, M.K., Meldal, M. and Bock, K., Synthesis of mannose 6-phosphate-containing disaccharide threonine building blocks and their use in solid-phase glycopeptide synthesis, J. Chem. Soc., Perkin Trans. 1, (1993) 1453-1460.
    • (1993) J. Chem. Soc., Perkin Trans. 1 , pp. 1453-1460
    • Christensen, M.K.1    Meldal, M.2    Bock, K.3
  • 63
    • 37049078313 scopus 로고
    • Glycosylation of phenols: Preparation of 1,2-cis and 1,2-trans glycosylated tyrosine derivatives to be used in solid-phase glycopeptide synthesis
    • Jensen, K.J., Meldal, M. and Bock, K., Glycosylation of phenols: preparation of 1,2-cis and 1,2-trans glycosylated tyrosine derivatives to be used in solid-phase glycopeptide synthesis, J. Chem. Soc., Perkin Trans., 1 (1993) 2119-2129.
    • (1993) J. Chem. Soc., Perkin Trans., 1 , pp. 2119-2129
    • Jensen, K.J.1    Meldal, M.2    Bock, K.3
  • 64
    • 37049066793 scopus 로고
    • Synthesis of glycosylated peptide templates-containing 6′-O-phosphorylated mannose disaccharides and their binding to the cation-independent mannose 6-phosphate receptor
    • Christensen, M.K., Meldal, M., Bock, K., Cordes, H., Mouritsen, S. and Elsner, H., Synthesis of glycosylated peptide templates-containing 6′-O-phosphorylated mannose disaccharides and their binding to the cation-independent mannose 6-phosphate receptor, J. Chem. Soc., Perkin Trans., 1 (1994) 1299-1310.
    • (1994) J. Chem. Soc., Perkin Trans., 1 , pp. 1299-1310
    • Christensen, M.K.1    Meldal, M.2    Bock, K.3    Cordes, H.4    Mouritsen, S.5    Elsner, H.6
  • 65
    • 37049067264 scopus 로고
    • A PEGA resin for use in the solid-phase chemical-enzymatic synthesis of glycopeptides
    • Meldal, M., Auzanneau, F.-I., Hindsgaul, O. and Palcic, M.M., A PEGA resin for use in the solid-phase chemical-enzymatic synthesis of glycopeptides, J. Chem. Soc., Chem. Commun. (1994) 1849-1850.
    • (1994) J. Chem. Soc., Chem. Commun. , pp. 1849-1850
    • Meldal, M.1    Auzanneau, F.-I.2    Hindsgaul, O.3    Palcic, M.M.4
  • 66
    • 84988080209 scopus 로고
    • Eine neue strategie zur festphasensynthese von O-glycopepteden uber 2-azidoglycopeptide
    • Paulsen, H., Bielfeldt, T., Peters, S., Meldal, M. and Bock, K., Eine neue strategie zur festphasensynthese von O-glycopepteden uber 2-azidoglycopeptide, Liebigs Annu. Chem. (1994) 369-379.
    • (1994) Liebigs Annu. Chem. , pp. 369-379
    • Paulsen, H.1    Bielfeldt, T.2    Peters, S.3    Meldal, M.4    Bock, K.5
  • 67
    • 0029102472 scopus 로고
    • A novel allylic anchor for solid-phase synthesis - Synthesis of protected and unprotected O-glycosylated mucin-type glycopeptides
    • Seitz, O. and Kunz, H., A novel allylic anchor for solid-phase synthesis - Synthesis of protected and unprotected O-glycosylated mucin-type glycopeptides, Angew. Chem., Int. Ed. Engl., 34 (1995) 803-805.
    • (1995) Angew. Chem., Int. Ed. Engl. , vol.34 , pp. 803-805
    • Seitz, O.1    Kunz, H.2
  • 68
    • 0027064742 scopus 로고
    • General methods for α- or β-O-ser/thr glycosides and glycopeptides. Solid-phase synthesis of O-glycosyl cyclic enkephalin analogues
    • Polt, R., Szabo, L., Treiberg, J., Li, Y. and Hruby, V., General methods for α- or β-O-ser/thr glycosides and glycopeptides. Solid-phase synthesis of O-glycosyl cyclic enkephalin analogues, J. Am. Chem. Soc., 114 (1992) 10249-10258.
    • (1992) J. Am. Chem. Soc. , vol.114 , pp. 10249-10258
    • Polt, R.1    Szabo, L.2    Treiberg, J.3    Li, Y.4    Hruby, V.5
  • 69
    • 0026056895 scopus 로고
    • O-Glycopeptides: A simple β-stereoselective glycosidation of serine and threonine via a favorable hydrogen bonding pattern
    • Szabo, L., Li, Y. and Polt, R., O-Glycopeptides: A simple β-stereoselective glycosidation of serine and threonine via a favorable hydrogen bonding pattern, Tetrahedron Lett., 32 (1991) 585-588.
    • (1991) Tetrahedron Lett. , vol.32 , pp. 585-588
    • Szabo, L.1    Li, Y.2    Polt, R.3
  • 70
    • 0029925295 scopus 로고    scopus 로고
    • Preparation of a glycopeptide analogue of type II collagen - Use of acid labile protective groups for carbohydrate moieties in solid phase synthesis of O-linked glycopeptides
    • Broddefalk, J., Bergquist, K.-E. and Kihlberg, J., Preparation of a glycopeptide analogue of type II collagen - Use of acid labile protective groups for carbohydrate moieties in solid phase synthesis of O-linked glycopeptides, Tetrahedron Lett., 37 (1996) 3011-3014.
    • (1996) Tetrahedron Lett. , vol.37 , pp. 3011-3014
    • Broddefalk, J.1    Bergquist, K.-E.2    Kihlberg, J.3
  • 74
    • 0030178498 scopus 로고    scopus 로고
    • Multiple-column synthesis of a library of T-cell stimulating Tn-antigenic glycopeptide analogues for the molecular characterization of T-cell-glycan specificity
    • Frische, K., Meldal, M., Werdelin, O., Mouritsen, S., Jensen, T., Galli-Stampino, L. and Bock, K., Multiple-column synthesis of a library of T-cell stimulating Tn-antigenic glycopeptide analogues for the molecular characterization of T-cell-glycan specificity, J. Pept. Sci., 2 (1996) 212-222.
    • (1996) J. Pept. Sci. , vol.2 , pp. 212-222
    • Frische, K.1    Meldal, M.2    Werdelin, O.3    Mouritsen, S.4    Jensen, T.5    Galli-Stampino, L.6    Bock, K.7
  • 75
    • 0029801847 scopus 로고    scopus 로고
    • Generation of C-glycoside peptide ligands for cell surface carbohydrate receptors using a four-component condensation on solid supports
    • Sutherlin, D.P., Stark, T.M., Hughes, R. and Armstrong, R.W., Generation of C-glycoside peptide ligands for cell surface carbohydrate receptors using a four-component condensation on solid supports, J. Org. Chem., 61 (1996) 8350-8354.
    • (1996) J. Org. Chem. , vol.61 , pp. 8350-8354
    • Sutherlin, D.P.1    Stark, T.M.2    Hughes, R.3    Armstrong, R.W.4
  • 76
    • 0000512227 scopus 로고    scopus 로고
    • Multiple-component condensation strategies for combinatorial library synthesis
    • Armstrong, R.W., Combs, A.P., Tempest, P.A., Brown, S.D. and Keating, T.A., Multiple-component condensation strategies for combinatorial library synthesis, Acc. Chem. Res., 29 (1996) 123-131.
    • (1996) Acc. Chem. Res. , vol.29 , pp. 123-131
    • Armstrong, R.W.1    Combs, A.P.2    Tempest, P.A.3    Brown, S.D.4    Keating, T.A.5
  • 77
    • 0028020837 scopus 로고
    • Strategies for the synthesis of C-disaccharides containing D and L sugars
    • Armstrong, R.W. and Sutherlin, D.P., Strategies for the synthesis of C-disaccharides containing D and L sugars, Tetrahedron Lett., 35 (1994) 7743-7746.
    • (1994) Tetrahedron Lett. , vol.35 , pp. 7743-7746
    • Armstrong, R.W.1    Sutherlin, D.P.2
  • 78
    • 0029860709 scopus 로고    scopus 로고
    • The synthesis of C-trisaccharides exploiting the stereochemical diversity of a central sugar
    • Sutherlin, D.P. and Armstrong, R.W., The synthesis of C-trisaccharides exploiting the stereochemical diversity of a central sugar, J. Am. Chem. Soc., 118 (1996) 9802-9803.
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 9802-9803
    • Sutherlin, D.P.1    Armstrong, R.W.2
  • 80
    • 0029905917 scopus 로고    scopus 로고
    • Rapid combinatorial synthesis of aminoglycoside antibiotic mimetics: Use of a polyethylene glycol-linked amine and a neamine-derived aldehyde in multiple component condensation as a strategy for the discovery of new inhibitors of the HIV RNA Rev responsive element
    • Park, W.K.C., Auer, M., Jaksche, H. and Wong, C.-H., Rapid combinatorial synthesis of aminoglycoside antibiotic mimetics: Use of a polyethylene glycol-linked amine and a neamine-derived aldehyde in multiple component condensation as a strategy for the discovery of new inhibitors of the HIV RNA Rev responsive element, J. Am. Chem. Soc., 118 (1996) 10150-10155.
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 10150-10155
    • Park, W.K.C.1    Auer, M.2    Jaksche, H.3    Wong, C.-H.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.