330596-38-8

Upstream product

• 302783-17-1 methyl 2,3-di-O-acetyl-4,6-O-p-methoxybenzylidene-α-D-glucopyranoside 
• 330596-36-6 methyl 2,3-di-O-acetyl-4-O-p-methoxybenzyl-α-D-glucopyranoside 

Downstream Products

• 330596-39-9 [4-(tert-Butyl-diphenyl-silanyloxymethyl)-2-nitro-phenoxy]-acetic acid (2R,3R,4S,5R,6S)-4,5-diacetoxy-3-hydroxy-6-methoxy-tetrahydro-pyran-2-ylmethyl ester 
• 330596-35-5 (4-Hydroxymethyl-2-nitro-phenoxy)-acetic acid (2R,3R,4S,5R,6S)-4,5-diacetoxy-3-(9H-fluoren-9-ylmethoxycarbonyloxy)-6-methoxy-tetrahydro-pyran-2-ylmethyl ester 
• 330596-40-2 [4-(tert-Butyl-diphenyl-silanyloxymethyl)-2-nitro-phenoxy]-acetic acid (2R,3R,4S,5R,6S)-4,5-diacetoxy-3-(9H-fluoren-9-ylmethoxycarbonyloxy)-6-methoxy-tetrahydro-pyran-2-ylmethyl ester 
• 604-70-6 Acetic acid (2R,3R,4S,5R,6S)-3,5-diacetoxy-2-acetoxymethyl-6-methoxy-tetrahydro-pyran-4-yl ester 

Relevant academic research and scientific papers

A new phenoxyacetate-based linker system for the solid-phase synthesis of oligosaccharides.

[structure: see text]. A novel linker system has been designed, and its first application to solid-phase oligosaccharide synthesis is described. The use of the highly reactive o-nitro-phenoxyacetate linker allows a fast and quantitative cleavage using mild basic conditions. This method combined with the trichloroacetimidate glycosylation exhibits highly promising results as demonstrated for the synthesis of tetrasaccharide 1 (n = 3) containing glucose beta(1 --> 4) and beta(1 --> 6) linkages.