89950-76-5

Upstream product

• 98-88-4 benzoyl chloride 
• 26301-79-1 D-mannono-1,4-lactone 

Downstream Products

• 218614-36-9 2,5,6-tri-O-benzoyl-3-O-(2,3,5,6-tetra-O-benzoyl-β-D-galactofuranosyl)-D-mannono-1,4-lactone 
• 218614-45-0 2,5,6-tri-O-benzoyl-3-O-(2,5,6-tri-O-benzoyl-3-deoxy-β-D-xylo-hexofuranosyl)-D-mannono-1,4-lactone 
• 1130007-95-2 2,3,5,6-tetra-O-tert-butyldimethylsilyl-β-D-galactofuranosyl-(1->3)-2,5,6-tri-O-benzoyl-D-mannono-1,4-lactone 
• 4144-97-2 O³-β-D-galactofuranosyl-D-mannitol 
• 125343-66-0 3,5,6-tri-O-benzoyl-2-O-methyl-D-mannono-1,4-lactone 

Relevant academic research and scientific papers

The glycosyl-aldonolactone approach for the synthesis of β-d-Galf-(1→3)-d-Manp and 3-deoxy-β-d-xylo-hexofuranosyl-(1→3)-d-Manp

A convenient synthesis of free β-d-Galf-(1→3)-d-Manp (8a) is reported. The disaccharide is present as external unit in the lipopeptidophosphoglycan (LPPG) of Trypanosoma cruzi and internally in the lipophosphoglycan (LPG) of Leishmania. Condensation of 2,

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