Methyl tetra-O-allyl, and tetra-O-[2-(tetrahydro-2H-pyranyl)oxy.-3-oxapentyl glucosides, and tetra-O-(cyanoethyl)galactosyl azide were converted into derivatives containing linkers with terminal carboxylic acid functionalities at the anomeric position and bearing four arms with phthaloyl- or BOC-protected terminal amino groups. These molecules were suitable for use in solid-phase peptide synthesis and for the preparation of dendrimers, containing multiple copies of peptides. (C) 2001 Elsevier Science Ltd. All rights reserved.
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Univ Grenoble Alpes, CNRS, DCM UMR 5250, F-38000 Grenoble, FranceUniv Grenoble Alpes, CNRS, DCM UMR 5250, F-38000 Grenoble, France
Pifferi, Carlo
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Berthet, Nathalie
Renaudet, Olivier
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Univ Grenoble Alpes, CNRS, DCM UMR 5250, F-38000 Grenoble, France
Inst Univ France, 103 Blvd St Michel, F-75005 Paris, FranceUniv Grenoble Alpes, CNRS, DCM UMR 5250, F-38000 Grenoble, France