메뉴 건너뛰기




Volumn 1, Issue 1, 1997, Pages 130-135

Combinatorial approaches to carbohydrates

Author keywords

[No Author keywords available]

Indexed keywords

CARBOHYDRATE;

EID: 0031152054     PISSN: 13675931     EISSN: None     Source Type: Journal    
DOI: 10.1016/s1367-5931(97)80119-6     Document Type: Article
Times cited : (47)

References (33)
  • 1
    • 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 1993, 3:97-130.
    • (1993) Glycobiology , vol.3 , pp. 97-130
    • Varki, A.1
  • 2
    • 0027339137 scopus 로고
    • Carbohydrates in cell recognition
    • Sharon N, Lis H: Carbohydrates in cell recognition. Sci Am 1993, 268:82.
    • (1993) Sci am , vol.268 , pp. 82
    • Sharon, N.1    Lis, H.2
  • 3
    • 0025877788 scopus 로고
    • Antibacterial activities and modes of action of vancomycin and related glycopeptides
    • Nagarajan R: Antibacterial activities and modes of action of vancomycin and related glycopeptides. Antimicrob Agents Chemother 1991, 605-609.
    • (1991) Antimicrob Agents Chemother , pp. 605-609
    • Nagarajan, R.1
  • 6
    • 0027643018 scopus 로고
    • Solid-phase synthesis and conformational studies of glycosylated derivatives of helper-T-cell immunogenic peptides from hen-egg lysozyme
    • Elofsson M, Roy S, Walse B, Kihlberg J: Solid-phase synthesis and conformational studies of glycosylated derivatives of helper-T-cell immunogenic peptides from hen-egg lysozyme. Carbohydrate Res 1993, 245:89-103.
    • (1993) Carbohydrate Res , vol.245 , pp. 89-103
    • Elofsson, M.1    Roy, S.2    Walse, B.3    Kihlberg, J.4
  • 7
    • 1842524152 scopus 로고    scopus 로고
    • Rational design of multivalent glycoconjugate ligands. Synthesis of libraries of conformationally flexible rotamers of poly-N-linked lactosyl glycines
    • Roy R, Saha UK: Rational design of multivalent glycoconjugate ligands. Synthesis of libraries of conformationally flexible rotamers of poly-N-linked lactosyl glycines. Chem Commun 1996, 201-202.
    • (1996) Chem Commun , pp. 201-202
    • Roy, R.1    Saha, U.K.2
  • 8
    • 0029801847 scopus 로고    scopus 로고
    • Generation of C-glycoside peptide ligands for cell surface carbohydrate receptors using a four-component condensation on solid support
    • Sutherlin DP, Stark TM, Hughes R, Armstrong RW: Generation of C-glycoside peptide ligands for cell surface carbohydrate receptors using a four-component condensation on solid support. J Org Chem 1996, 61:8350-8354.
    • (1996) J Org Chem , vol.61 , pp. 8350-8354
    • Sutherlin, D.P.1    Stark, T.M.2    Hughes, R.3    Armstrong, R.W.4
  • 9
    • 0028577515 scopus 로고
    • Isolation and characterization of natural protein-associated carbohydrate ligands for E-selectin
    • Patel TP, Goelz SE, Lobb RR, Parekh RB: Isolation and characterization of natural protein-associated carbohydrate ligands for E-selectin. Biochemistry 1994, 33:14815-14824.
    • (1994) Biochemistry , vol.33 , pp. 14815-14824
    • Patel, T.P.1    Goelz, S.E.2    Lobb, R.R.3    Parekh, R.B.4
  • 11
    • 33751134981 scopus 로고
    • A strategy of 'random glycosylation' for the production of oligosaccharide libraries
    • Hindsgaul O: A strategy of 'random glycosylation' for the production of oligosaccharide libraries. Angew Chem Int Ed 1995, 34:2720-2722. An imaginative approach to carbohydrate libraries. Remarkably, glycosylation of unprotected acceptors containing both primary and secondary alcohols produces equivalent distribution of products.
    • (1995) Angew Chem int Ed , vol.34 , pp. 2720-2722
    • Hindsgaul, O.1
  • 12
    • 0028790946 scopus 로고
    • Synthesis and biological activity of oligosaccharide libraries
    • Edited by Alavi A, Axford JS. New York: Plenum Press
    • Ding Y, Kanie O, Labbe J, Palcic MM, Ernst B, Hindsgaul O: Synthesis and biological activity of oligosaccharide libraries. In Glycoimmunology. Edited by Alavi A, Axford JS. New York: Plenum Press; 1995:261-269.
    • (1995) Glycoimmunology , pp. 261-269
    • Ding, Y.1    Kanie, O.2    Labbe, J.3    Palcic, M.M.4    Ernst, B.5    Hindsgaul, O.6
  • 13
    • 0029895067 scopus 로고    scopus 로고
    • Towards oligosaccharide libraries: A study of the random galactosylation of unprotected N-acetylglucosamine
    • Ding Y, Labbe J, Kanie O, Hindsgaul O: Towards oligosaccharide libraries: a study of the random galactosylation of unprotected N-acetylglucosamine. Bioorg Med Chem 1996, 4:683-692.
    • (1996) Bioorg Med Chem , vol.4 , pp. 683-692
    • Ding, Y.1    Labbe, J.2    Kanie, O.3    Hindsgaul, O.4
  • 14
    • 0030484272 scopus 로고    scopus 로고
    • Vinyl glycosides in oligosaccharide synthesis: A strategy for the preparation of trisaccharide libraries based on latent-active glycosylation
    • Boons GJ, Heskamp B, Hout F: Vinyl glycosides in oligosaccharide synthesis: a strategy for the preparation of trisaccharide libraries based on latent-active glycosylation. Angew Chem Int Ed 1996, 35:2845-2847.
    • (1996) Angew Chem int Ed , vol.35 , pp. 2845-2847
    • Boons, G.J.1    Heskamp, B.2    Hout, F.3
  • 15
    • 10544229790 scopus 로고    scopus 로고
    • Parallel synthesis and screening of a solid phase carbohydrate library
    • Liang R, Yan L, Loebach J, Ge M, Uozumi Y, Sekanina K, Horan N, Gildersleeve J, Thompson C, Smith A et al.: Parallel synthesis and screening of a solid phase carbohydrate library. Science 1996, 274:1520-1522. The first solid-phase combinatorial synthesis of a carbohydrate library. Parallel screening shows remarkable specificity for polyvalent carbohydrate - protein interactions.
    • (1996) Science , vol.274 , pp. 1520-1522
    • Liang, R.1    Yan, L.2    Loebach, J.3    Ge, M.4    Uozumi, Y.5    Sekanina, K.6    Horan, N.7    Gildersleeve, J.8    Thompson, C.9    Smith, A.10
  • 17
    • 33751157590 scopus 로고
    • A general method for molecular tagging of encoded combinatorial chemistry libraries
    • Nestler HP, Bartlett PA, Still WC: A general method for molecular tagging of encoded combinatorial chemistry libraries. J Org Chem 1994, 59:4723-4724.
    • (1994) J Org Chem , vol.59 , pp. 4723-4724
    • Nestler, H.P.1    Bartlett, P.A.2    Still, W.C.3
  • 18
    • 0342487255 scopus 로고
    • Polymer-supported synthesis of oligosaccharides
    • Edited by Hodge P, Sherrington DC. New York: John Wiley & Sons;
    • Frecht JMJ: Polymer-supported synthesis of oligosaccharides. In Polymer-Supported Reactions in Organic Synthesis. Edited by Hodge P, Sherrington DC. New York: John Wiley & Sons; 1980:407.
    • (1980) Polymer-Supported Reactions in Organic Synthesis , pp. 407
    • Frecht, J.M.J.1
  • 19
    • 0042577281 scopus 로고
    • Preparation of a fragment of the cell wall teichoic acid of Bacillus licheniformis ATCC 9945 via a solid phase approach
    • Westerduin P, Veeneman GH, Pennings Y, van der Marel GA, van Boom JH: Preparation of a fragment of the cell wall teichoic acid of Bacillus licheniformis ATCC 9945 via a solid phase approach. Tetrahedron Lett 1987, 28:1557-1560.
    • (1987) Tetrahedron Lett , vol.28 , pp. 1557-1560
    • Westerduin, P.1    Veeneman, G.H.2    Pennings, Y.3    Van Der Marel, G.A.4    Van Boom, J.H.5
  • 20
    • 0000462978 scopus 로고
    • Solid-phase synthesis of a naturally occurring β-(1→5)-linked D-galactofuranosyl heptamer containing the artificial linkage arm L-homoserine
    • Veeneman GH, Notermans S, Liskamp RMJ, van der Marel GA, van Boom JH: Solid-phase synthesis of a naturally occurring β-(1→5)-linked D-galactofuranosyl heptamer containing the artificial linkage arm L-homoserine. Tetrahedron Lett 1987, 28:6695-6698.
    • (1987) Tetrahedron Lett , vol.28 , pp. 6695-6698
    • Veeneman, G.H.1    Notermans, S.2    Liskamp, R.M.J.3    Van Der Marel, G.A.4    Van Boom, J.H.5
  • 21
    • 0025707215 scopus 로고
    • Solid-phase synthesis of a cell-wall component of Haemophilus (Actinobacillus) pleuropneumoniae serotype 2
    • Veeneman GH, Brugghe HF, van den Elst H, van Boom JH: Solid-phase synthesis of a cell-wall component of Haemophilus (Actinobacillus) pleuropneumoniae serotype 2. Carbohydrate Res 1990, 195:C1-C4.
    • (1990) Carbohydrate Res , vol.195
    • Veeneman, G.H.1    Brugghe, H.F.2    Van Den Elst, H.3    Van Boom, J.H.4
  • 24
    • 0029007777 scopus 로고
    • Major simplifications in oligosaccharide synthesis arising from a solid-phase method: An application to the synthesis of the Lewis b antigen
    • Randolph JT, McClure KF, Danishefsky SJ: Major simplifications in oligosaccharide synthesis arising from a solid-phase method: an application to the synthesis of the Lewis b antigen. J Am Chem Soc 1995, 117:5712-5719.
    • (1995) J am Chem Soc , vol.117 , pp. 5712-5719
    • Randolph, J.T.1    McClure, K.F.2    Danishefsky, S.J.3
  • 25
    • 0027951227 scopus 로고
    • Solid-phase chemical-enzymatic synthesis of glycopeptides and oligosaccharides
    • Schuster M, Wang P, Paulson JC, Wong CH: Solid-phase chemical-enzymatic synthesis of glycopeptides and oligosaccharides. J Am Chem Soc 1994, 116:1135-1136.
    • (1994) J am Chem Soc , vol.116 , pp. 1135-1136
    • Schuster, M.1    Wang, P.2    Paulson, J.C.3    Ch, W.4
  • 26
    • 0000508254 scopus 로고
    • Glycosylation on the Merrifield resin using anomeric sulfoxides
    • Yan L, Taylor CM, Goodnow R Jr, Kahne D: Glycosylation on the Merrifield resin using anomeric sulfoxides. J Am Chem Soc 1994, 116:6953-6954.
    • (1994) J am Chem Soc , vol.116 , pp. 6953-6954
    • Yan, L.1    Taylor, C.M.2    Jr, G.R.3    Kahne, D.4
  • 27
    • 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 SP, Whitfield DM, Krepinsky JJ: 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 1995, 117:2116-2117. Efficient and general strategy for synthesis of oligosaccharides on a soluble polymer. The approach combines advantages of both solid-phase and solution synthesis and may provide useful therapeutics.
    • (1995) J am Chem Soc , vol.117 , pp. 2116-2117
    • Douglas, S.P.1    Whitfield, D.M.2    Krepinsky, J.J.3
  • 28
    • 0029958313 scopus 로고    scopus 로고
    • Solid-phase synthesis of 6-deoxyoligosaccharides
    • Hunt JA, Roush WR: Solid-phase synthesis of 6-deoxyoligosaccharides. J Am Chem Soc 1996, 118:9998-9999.
    • (1996) J am Chem Soc , vol.118 , pp. 9998-9999
    • Hunt, J.A.1    Roush, W.R.2
  • 29
    • 0030445494 scopus 로고    scopus 로고
    • Orthogonal glycosylation strategy for rapid assembly of oligosaccharides on a polymer support
    • Ito Y, Kanie O, Ogawa T: Orthogonal glycosylation strategy for rapid assembly of oligosaccharides on a polymer support Angew Chem Int Ed 1996, 35:2510-2512.
    • (1996) Angew Chem int Ed , vol.35 , pp. 2510-2512
    • Ito, Y.1    Kanie, O.2    Ogawa, T.3
  • 30
    • 0029996782 scopus 로고    scopus 로고
    • A new method for the solid phase synthesis of oligosaccharides
    • Rademann J, Schmidt RR: A new method for the solid phase synthesis of oligosaccharides. Tetrahedron Lett 1996, 37:3989-3990.
    • (1996) Tetrahedron Lett , vol.37 , pp. 3989-3990
    • Rademann, J.1    Schmidt, R.R.2
  • 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 KC, Winssinger N, Pastor J, DeRoose F: A general and highly efficient solid phase synthesis of oligosaccharides. Total synthesis of a heptasaccharide phytoalexin elicitor (HPE). J Am Chem Soc 1997, 119:449-450. A highly convergent synthesis of a large oligosaccharide on the solid phase. This work establishes that it is feasible - and possibly preferable in many cases - to make large oligosaccharides on a solid support.
    • (1997) J am Chem Soc , vol.119 , pp. 449-450
    • Nicolaou, K.C.1    Winssinger, N.2    Pastor, J.3    DeRoose, F.4
  • 32
    • 0031080051 scopus 로고    scopus 로고
    • Glycosphingolipid antigens and cancer therapy
    • Hakomori S, Zhang Y: Glycosphingolipid antigens and cancer therapy. Chem Biol 1997, 4:97-104.
    • (1997) Chem Biol , vol.4 , pp. 97-104
    • Hakomori, S.1    Zhang, Y.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.