110319-36-3

Upstream product

• 2595-07-5 allyl β-D-galactopyranoside 
• 58479-61-1 tert-butylchlorodiphenylsilane 

Downstream Products

• 110319-41-0 allyl 6-O-(tert-butyldiphenylsilyl)-2,3,4-tris-O-(p-phenylbenzoyl)-β-D-galactopyranoside 
• 110319-52-3 allyl O-(2,3,4,6-tetra-O-benzoyl-β-D-galactopyranosyl)-(1<*>6)-2,3,4-tris-O-(p-phenylbenzoyl)-β-D-galactopyranoside 
• 110319-45-4 allyl 2,3,4-tris-O-(phenylbenzoyl)-β-D-galactopyranoside 
• 749858-85-3 Acetic acid (2R,3S,4S,5R,6R)-4,5-diacetoxy-6-allyloxy-2-(tert-butyl-diphenyl-silanyloxymethyl)-tetrahydro-pyran-3-yl ester 
• 749858-86-4 Acetic acid (2R,3S,4S,5R,6R)-4,5-diacetoxy-2-(tert-butyl-diphenyl-silanyloxymethyl)-6-(2,2,2-trichloro-acetimidoyloxy)-tetrahydro-pyran-3-yl ester 

Relevant academic research and scientific papers

Rapid oligosaccharide synthesis using a fluorous protective group

The Bfp-OH, a novel fluorous protecting reagent, was able to be easily prepared. The Bfp group was readily introduced to a carbohydrate, removed in high yield, and recyclable after cleavage. The use of the Bfp group made it possible to synthesize a pentasaccharide by minimal column chromatography purification. Each synthetic intermediate was able to be easily purified only by simple fluorous-organic solvent extraction and monitored by TLC, NMR, and MS.

Selective Silylation of β-D-Galactosides. A New Approach to the Synthesis of (1->6)-β-D-Galactopyranooligosaccharides.

A simple and convenient synthesis of β-D-galactopyranose derivatives selectively modified at C-1 and C-6 is described.A key feature is the selective protection of the 6-OH group of methyl-, allyl-,and (p-nitrophenyl)-β-D-galactopyranosides using tert-buty