30694-75-8

Upstream product

• 55263-78-0 1,2-O-isopropylidene-5-O-toluene-p-sulphonyl-α-D-glucofuranurono-6,3-lactone 
• 55263-78-0 1,2-O-isopropylidene-5-O-tosyl-α-D-glucuronolactone 
• 487-44-5 D-(+)-glucuronic acid γ-lactone 
• 20513-98-8 1,2-O-isopropylidene-α-D-glucofuranurono-6,3-lactone 

Downstream Products

• 73892-49-6 benzyl 1,2-O-isopropylidene-5-O-toluene-p-sulphonyl-(6S)-α-D-gluco-hexodialdo-1,4-furanose-6,3-furanoside 
• 73892-50-9 6-O-benzoyl-1,2-O-isopropylidene-5-O-toluene-p-sulphonyl-(6S)-α-D-gluco-hexodialdo-1,4:6,3-difuranose 
• 73892-50-9 6-O-benzoyl-1,2-O-isopropylidene-5-O-toluene-p-sulphonyl-(6R)-α-D-gluco-hexodialdo-1,4:6,3-difuranose 
• 73351-54-9 6-O-acetyl-5-O-benzoyl-1,2-O-isopropylidene-(6S)-β-L-ido-hexodialdo-1,4:6,3-difuranose 
• 488-45-9 L-iditol 
• 62102-45-8 2,3,4,5-tetra-O-benzyl-L-iditol 
• 94926-00-8 2,5-di-O-benzyl-L-iditol 
• 110522-64-0 (2S,3S,3aS,5S,6R,6aS)-3,6-Bis-benzyloxy-2,5-dimethoxy-hexahydro-furo[3,2-b]furan 
• 110522-69-5 (2S,3R,4R,5S)-3,4-Bis-allyloxy-2,5-bis-benzyloxy-hexane-1,6-diol 
• 110522-70-8 3,4-di-O-allyl-2,5-di-O-benzyl-L-ido-hexodialdose 
• 62102-44-7 2,3,4,5-tetra-O-benzyl-D-ido-hexodialdose 
• 110522-66-2 (2S,3S,4S,5S)-2,5-Bis-benzyloxy-1,6-bis-trityloxy-hexane-3,4-diol 
• 110522-68-4 C₆₄H₆₂O₆ 
• 110522-67-3 C₇₂H₆₆O₆ 

Relevant academic research and scientific papers

Synthesis of Optically Active Inositol Derivatives Starting from D-Glucurono-6,3-lactone

D-Glucurono-6,3-lactone was converted to optically active and partially protected inositols.The synthetic strategy involves an efficient conversion of the D-gluco configuration to the L-ido configuration and dials to cyclitols.

SYNTHESIS OF L-IDOFURANURONO-6,3-LACTONE AND ITS DERIVATIVES via HEXODIALDODIFURANOSES

1,2-O-Alkylidene-β-L-idofuranurono-6,3-lactones were obtained from the corresponding 5-O-toluene-p-sulphonyl-α-D-glucofuranurono-6,3-lactones by a sequence involving lactone reduction, benzoylation of HO-6, inversion of configuration at C-5, deacylation,