59464-21-0

Upstream product

• 58394-32-4 1,6-anhydro-2,3-dideoxy-β-threo-hex-2-enopyranose 
• 6893-59-0 1,6:2,3-dianhydro-β-D-talopyranose 
• 100-39-0 benzyl bromide 
• 21193-75-9 D-galactal 
• 174905-26-1 3-O-Acetyl-1,6-anhydro-4-O-benzyl-2-bromo-2-deoxy-β-D-galactopyranose 
• 141054-99-1 1,6-anhydro-4-O-benzyl-2,3-dideoxy-β-D-threo-hex-2-enopyranose 
• 61074-28-0 1,6:2,3-di-anhydro-4-O-benzyl-β-D-talopyranose 

Downstream Products

• 67817-35-0 3,6-di-O-acetyl-2-azido-4-O-benzyl-2-deoxy-α-D-galactopyranosyl bromide 
• 1226996-83-3 1,6-anhydro-2-azido-4-O-benzyl-2-deoxy-3-O-tosyl-β-D-galactopyranose 
• 88509-56-2 2-Acetamido-1,6-anhydro-4-O-benzyl-2-desoxy-3-O-(2,3,4-tri-O-benzyl-β-L-rhamnopyranosyl)-β-D-galactopyranosid 
• 88509-57-3 2-Acetamido-1,6-anhydro-4-O-benzyl-2-desoxy-3-O-(2,3,4-tri-O-benzyl-α-L-rhamnopyranosyl)-β-D-galactopyranosid 
• 2374-40-5 2-Acetamido-2-desoxy-3-O-β-L-rhamnopyranosyl-D-galactopyranose 
• 120633-77-4 C₄₆H₅₁N₉O₁₇ 
• 88509-58-4 3-O-(4-O-Allyl-2,3-di-O-benzyl-β-L-rhamnopyranosyl)-1,6-anhydro-2-azido-4-O-benzyl-2-desoxy-β-D-galactopyranose 

Relevant academic research and scientific papers

A Convenient Route to Peracetylated 3-Deoxy-3-fluoro Analogues of d -Glucosamine and d -Galactosamine from a ?erny Epoxide

Peracetylated 3-deoxy-3-fluoro analogues of d-glucosamine and d-galactosamine 3 and 4, respectively, were prepared from 1,6:2,3-dianhydro-4-O- benzyl-β-d-mannopyranose (6). Azidolysis of 6 followed by reaction with diethylaminosulfur trifluoride gave 1,6-

Reactions of 2-hydroxy-6,8-dioxabicyclo[3.2.1]oct-3-ene with diethylaminosulfur trifluoride and with halogens. Facile synthesis of 1,6- anhydrohalohexopyranoses

D-Galactal 1 reacts in THF in the presence of catalytic amounts of concentrated sulfuric acid to give (2R)-2-hydroxy-6,8-dioxabicyclo[3.2.1]oct- 3-ene (4) in a Ferrier-type rearrangement in 40% yield. When 4 is treated with diethylaminosulfur trifluoride

Synthesis of two analogues of a fragment of the complex polysaccharide C substance from Streptococcus pneumoniae type 1

The syntheses of two (spacer-containing and choline-phosphate-deficient) analogues (12e and 12h, Scheme 2) of a fragment of the C substance from S. pneumoniae type 1 are presented.Starting from 1,6:2,3-dianhydro-β-D-talopyranose (1a), the "building block"