Methyl tetra-O-allyl, and tetra-O-[2-(tetrahydro-2H-pyranyl)oxy.-3-oxapenty
l glucosides, and tetra-O-(cyanoethyl)galactosyl azide were converted into
derivatives containing linkers with terminal carboxylic acid functionalitie
s at the anomeric position and bearing four arms with phthaloyl- or BOC-pro
tected terminal amino groups. These molecules were suitable for use in soli
d-phase peptide synthesis and for the preparation of dendrimers, containing
multiple copies of peptides. (C) 2001 Elsevier Science Ltd. All rights res
erved.