R L Polt 1 , L Szabo , J Ramza
1. Department of Chemistry, University of Arizona, Tucson, USA.
Published:
GICID: 01.3001.0000.3100
Available language versions: en pl
Issue: Postepy Hig Med Dosw 1996; 50 (5)
Abstract
The diphenylketone Shiff-base appeared to be a very good protection from amino groups of serine and threonine for glycosylation reaction. O-Glycosides of these amino acids with different monosaccharides, aminosugars and deoxysugars were obtained with excellent yield and very high stereoselectivity. Products of glycosylation reactions were used as building blocks for solid phase glycopeptide synthesis.