Preparation of building blocks for glycopeptide synthesis by glycosylation of Fmoc amino acids having unprotected carboxyl groups

Tetrahedron

Volumn 51, Issue 19, 1995, Pages 5643-5656

  Salvador, Lourdes A ^a   Elofsson, Mikael ^a   Kihlberg, Jan ^a  

^a LUND INSTITUTE OF TECHNOLOGY   (Sweden)

Author keywords

[No Author keywords available]

Indexed keywords

GLYCOPEPTIDE;

ARTICLE; CARBOHYDRATE SYNTHESIS; GLYCOSYLATION; METHODOLOGY; PRIORITY JOURNAL; REACTION ANALYSIS;

EID: 0028943246     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4020(95)00224-V     Document Type: Article

References (45)

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2. Glycopeptide Synthesis
3. BF3--Etherate Induced Formation of 2,2,2-Trichloroethyl Glycopyranosides. Selective Visualization of Carbohydrate Derivatives on TLC Plates.
4. A NEW SYNTHESIS OF β-GLUCOPYRANOSIDES
5. Improved method for the synthesis of o-glycosylated fmoc amino acids to be used in solid-phase glycopeptide synthesis (Fmoc = fluoren-9-ylmethoxycarbonyl)
6. 1,2-Orthoacetate intermediates in silver trifluoromethanesulphonate promoted Koenigs–Knorr synthesis of disaccharide glycosides
7. Studies on Koenigs-Knorr Glycosidations.
8. Synthesis and biological activity of O-glycosylated morphiceptin analogues
9. A study of 13CH coupling constants in hexopyranoses
10. Building blocks for solid-phase glycopeptide synthesis: 2-acetamido-2-deoxy-?-D-glycosides of FmocSerOH and FmocThrOH
11. Glycosylation of phenols: preparation of 1,2-cis and 1,2-trans glycosylated tyrosine derivatives to be used in solid-phase glycopeptide synthesis
12. Small-scale solid-phase O-glycopeptide synthesis of linear and cyclized hexapeptides from blood-clotting factor IX containing O-(?-D-Xyl-1?3-?-D-Xyl-1?3-?-D-Glc)-L-ser
13. Synthesis of glycosyltyrosine building blocks for solid-phase glycopeptide assembly: use of aryl tert-butyl ethers as glycosyl acceptors in aromatic glycosylations
14. Observations on Silver Trifluoromethane Sulfonate-promoted Syntheses of 1,2-trans-Glycosides from Acylated Glycosyl Bromides.
15. Synthesis ofN-2,2,2-(Trichloroethoxycarbonyl)-L-amino Acids andN-(9-Fluorenylmethoxycarbonyl)-L-amino Acids Involving Succinimidoxy Anion as a Leaving Group in Amino Acid Protection
16. Convenient synthesis of O-(2-acitamido-2-deoxy-?-D-glucopyranosyl)-serine and -threonine building blocks for solid-phase glycopeptide assembly