35556-50-4

Upstream product

• 98-88-4 benzoyl chloride 
• 2782-07-2 D-galactono-1,4-lactone 

Downstream Products

• 5531-48-6 2,3,5,6-tetra-O-benzoyl-D-galactofuranose 
• 89202-34-6 1,2,3,5,6-penta-O-benzoyl-β-D-galactofuranoside 
• 35477-66-8 2,6-Di-O-benzoyl-3,5-dideoxy-D,L-threo-hexono-1,4-lactone 
• 153809-64-4 dibenzyl 2,3,5,6-tetra-O-benzoyl-α-D-galactofuranosyl-1-phosphate 
• 153923-40-1 2,3,5,6-tetra-O-benzoyl-β-D-galactofuranosyl bromide 
• 138811-45-7 1,2,3,5,6-penta-O-benzoyl-D-galactofuranose 
• 502696-57-3 3,5,6-tri-O-benzoyl-2-deoxy-D-lyxo-hexono-1,4-lactone 
• 35478-04-7 2,6-Dibenzoyloxo-2,4-hexadiene-4-olide 

Relevant academic research and scientific papers

Studies of UDP-galactopyranose mutase from Escherichia coli: An unusual role of reduced FAD in its catalysis

The galactofuranose moiety found in many surface constituents of microorganisms is derived from UDP-D-galactopyranose (UDP-Galp) via a unique ring contraction reaction catalyzed by UDP-Galp mutase. This enzyme, which has been isolated from several bacteri

Synthesis of glyceryl glycosides related to A-type prymnesin toxins

A suite of glycosylated glycerol derivatives representing various fragments of the glycosylated ichthyotoxins called prymnesins were chemically synthesised. Glycerol was used to represent a small fragment of the prymnesin backbone, and was glycosylated at

REGIOSELECTIVE ACYLATIONS OF ALDONO-1,4-LACTONES

Partial benzoylation or pivaloylation of D-gulono-1,4-lactone (1) with 3.3-3.6 molar equivalents of the acyl chloride afforded 2,5,6-tri-O-benzoyl- (3) or 2,5,6-tri-O-pivaloyl-D-gulono-1,4-lactone (5), which were isolated crystalline from the reaction mix