Building blocks for glycopeptide synthesis: glycosylation of 3-mercaptopropionic acid and Fmoc amino acids with unprotected carboxyl groups

Tetrahedron Letters

Volumn 32, Issue 51, 1991, Pages 7613-7616

  Elofsson, Mikael ^a   Walse, Björn ^a   Kihlberg, Jan ^a  

^a LUND INSTITUTE OF TECHNOLOGY   (Sweden)

Author keywords

glycopeptide; Glycosylated amino acid; Lewis acid; minimal protection; peracetylated glycosyl donor

Indexed keywords

GLYCOPEPTIDE;

ARTICLE; PEPTIDE SYNTHESIS; PRIORITY JOURNAL;

EID: 0026354455     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4039(91)80548-K     Document Type: Article

References (20)

1. Synthesis of Glycopeptides, Partial Structures of Biological Recognition Components[New Synthetic Methods(67)]
2. Synthesis of O-Glycopeptiden
3. Pentafluorophenyl esters for the temporary protection of the ?-carboxy group in solid phase glycopeptide synthesis
4. Protecting-Group-Dependent Stability of Intersaccharide Bonds?Synthesis of a Fucosyl-Chitobiose Glycopeptide
5. BF3--Etherate Induced Formation of 2,2,2-Trichloroethyl Glycopyranosides. Selective Visualization of Carbohydrate Derivatives on TLC Plates.
6. Improved method for the synthesis of o-glycosylated fmoc amino acids to be used in solid-phase glycopeptide synthesis (Fmoc = fluoren-9-ylmethoxycarbonyl)