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Glycopeptides solid-phase

Elongation of the peptide chain in the direction of the N-terminal by a solid-phase procedure was introduced by Lavielle and coworkers,132 who prepared the glycopeptide [3-0-(2-acetamido-2-deoxy-/ -D-gluco-pyranosyl)-L-serine]-L-glycyl-L-alanine (189) by first coupling 168, de-protected by hydrogenolysis, to an L-alanyl resin (188), and, after re-... [Pg.173]

Haase C, Seitz O (2007) Chemical Synthesis of Glycopeptides. 267 1-36 Hahn F, Schepers U (2007) Solid Phase Chemistry for the Directed Synthesis of Biologically Active Polyamine Analogs, Derivatives, and Conjugates. 278 135-208 Hansen SG, Skrydstrup T (2006) Modification of Amino Acids, Peptides, and Carbohydrates through Radical Chemistry. 264 135-162... [Pg.259]

Seitz O, Kunz H. HYCRON, an allylic anchor for high-efficiency solid phase synthesis of protected peptides and glycopeptides. J Org Chem 1997 62 813-826. [Pg.221]

Nakamura K, Hanai N, Kanno M, Kobayashi A, Ohnishi Y, Ito Y, Nakahara Y. Design and synthesis of silyl ether-based linker for solid-phase synthesis of glycopeptides. Tetrahedron Lett 1999 40 515-518. [Pg.221]

J. Vondrasek, and M. Pisacka, Solid phase synthesis of glycopeptide dendrimers with Tn antigenic structure and their biological activities. Part I, J. Pept. Sci., 5 (1999) 46-55. [Pg.385]

Urge, L., Kollat, E., Hollosi, M., Laczko, I., Wroblewski, K., Thurin, J., and Otvos Jr., L. (1991) Solid-phase synthesis of glycopeptides synthesis of Na-fluorenylmethoxycarbonyl L-asparagine Nb-glyco-sides. Tetrahedron Lett. 32, 3445-3448. [Pg.1123]

Scheme 4.77 Preparation of solid-phase glycopeptide library [411,412],... Scheme 4.77 Preparation of solid-phase glycopeptide library [411,412],...
The solid-phase synthesis of glycopeptides was first realized by applying the polymeric benzyl ester principle of Merrifield. According to this methodology, Lavielle and associates (50) used 7V-(tm-butyloxycarbonyl)-<9-glycosyl serine derivative 153 for condensation with resin-linked alanine 154. [Pg.299]

Otvos et al. (27) adopted the Fmoc-pentafluorophenyl ester methodology and have applied O-deacetylated glycopeptide intermediates (170 and 171) for solid-phase synthesis of glycopeptides. In this way, the A-glycopep-tide (26) H-Gly-L-Lys-L-Ala-L-Tyr-L-Thr-L-Ile-L-Phe-L-... [Pg.302]

Solid-Phase Synthesis of Biologically Important Glycopeptides... [Pg.257]

Sequential solid-phase glycopeptide synthesis using glycosylated amino acid building blocks... [Pg.257]

The most effective and general route to synthetic glycopeptides includes the employment of glycosylated amino acids in stepwise solid-phase syntheses based on... [Pg.257]

SOLID-PHASE SYNTHESIS OF BIOLOGICALLY IMPORTANT GLYCOPEPTIDES... [Pg.258]

Scheme 13.7 Solid-phase synthesis of a glycopeptide from the homophilic recognition domain of epithelial Cadherin 1 using the new coupling reagent PfPyU. Scheme 13.7 Solid-phase synthesis of a glycopeptide from the homophilic recognition domain of epithelial Cadherin 1 using the new coupling reagent PfPyU.

See other pages where Glycopeptides solid-phase is mentioned: [Pg.279]    [Pg.279]    [Pg.15]    [Pg.354]    [Pg.203]    [Pg.151]    [Pg.153]    [Pg.168]    [Pg.3]    [Pg.167]    [Pg.228]    [Pg.296]    [Pg.299]    [Pg.309]    [Pg.317]    [Pg.89]    [Pg.90]    [Pg.182]    [Pg.280]    [Pg.282]    [Pg.287]    [Pg.288]    [Pg.302]    [Pg.306]    [Pg.20]    [Pg.32]    [Pg.36]    [Pg.37]    [Pg.257]    [Pg.258]    [Pg.260]    [Pg.261]    [Pg.265]   
See also in sourсe #XX -- [ Pg.299 , Pg.300 , Pg.301 , Pg.302 , Pg.306 ]




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Glycopeptide

Glycopeptides

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