118358-79-5

Upstream product

• 118358-66-0 N-(9-fluorenylmethyloxycarbonyl)-L-serine benzyl ester 
• 65982-19-6 2,3,4,6-tetra-O-acetyl-D-monnopyranosyl chloride 
• 13242-53-0 acetobromomannose 
• 121238-27-5 2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl trichloroimidate 

Downstream Products

• 118358-80-8 N-(9-fluorenylmethyloxycarbonyl)-O-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-L-serine 
• 78609-14-0 O-α-D-mannopyranosyl-L-serine 
• 148905-24-2 2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl-L-serine benzyl ester 

Relevant academic research and scientific papers

From solution phase to "on-column" chemistry: Trichloroacetimidate-based glycosylation promoted by perchloric acid-silica

Activation of ester-protected glycosyl trichloroacetimidate donors by perchloric acid immobilized on silica afforded 1,2-trans disaccharides in 60-90% yields. Applying this approach to one-pot sequential glycosylation resulted in efficient syntheses of th

Glycosylation of Fmoc amino acids: Preparation of mono- and di-glycosylated derivatives and their incorporation into Arg-Gly-Asp (RGD)-containing glycopeptides

Compounds containing O-glycosidic linkages between carbohydrate species (D-glucopyranose, D-mannopyranose and L-rhamnopyranose) and hydroxy-containing amino acid components (L-threonine, L-serine and L-hydroxyproline) have been synthesized. Significant qu

Synthesis and conformational and NMR studies of α-D-mannopyranosyl and α-D-mannopyranosyl-(1-->2)-α-D-mannopyranosyl linked to L-serine and L-threonine

α-D-Mannopyranosyl and α-D-mannopyranosyl-(1-->2)-α-D-mannopyranosyl linked to L-serine and L-threonine have been synthesised as model substances for the linkage region in certain O-linked glycoproteins.Metropolis Monte Carlo simulations were performed wi