121403-55-2

Upstream product

• 121403-53-0 6-O-benzoyl-3-O-benzyl-1,2-O-isopropylidene-5-C-nitromethyl-α-D-glucofuranose 
• 121403-54-1 (R)-2-((3aR,5S,6S,6aR)-6-Benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-1-(tert-butyl-dimethyl-silanyloxy)-3-nitro-propan-2-ol 
• 121403-58-5 Benzoic acid (R)-2-((3aR,5R,6S,6aR)-6-benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-3-nitro-propyl ester 
• 121403-59-6 [(R)-2-((3aR,5R,6S,6aR)-6-Benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-3-nitro-propoxy]-tert-butyl-dimethyl-silane 
• 106445-05-0 3-O-benzyl-6-O-tert-butyldimethylsilyl-1,2-O-isopropylidene-α-D-xylo-hexofuran-5-ulose 
• 106445-04-9 1-(6-benzyloxy-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-5-yl)-2-(tert-butyldimethylsiloxy)ethanol 
• 121403-60-9 C₂₄H₂₆⁽²⁾HNO₈ 
• 121403-51-8 6-O-benzoyl-3-O-benzyl-1,2-O-isopropylidene-5-oxo-D-glucofuranose 
• 37776-15-1 6-O-Benzoyl-3-O-benzyl-1,2-O-isopropylidene-α-D-glucofuranose 
• 22529-61-9 (1R)-1-((3aR,6S,6aR)-6-(benzyloxy)-2,2-dimethyltetrahydrofuro(2,3-d)(1,3)dioxol-5-yl)ethane-1,2-diol 
• 77-76-9 2,2-dimethoxy-propane 
• 121403-53-0 6-O-benzoyl-3-O-benzyl-1,2-O-isopropylidene-5-C-nitromethyl-β-L-idofuranose 
• 121403-54-1 (S)-2-((3aR,5S,6S,6aR)-6-Benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-1-(tert-butyl-dimethyl-silanyloxy)-3-nitro-propan-2-ol 
• 121403-58-5 Benzoic acid (S)-2-((3aR,5R,6S,6aR)-6-benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-3-nitro-propyl ester 

Downstream Products

• 94943-08-5 (1S)-(+)-(1,3/2,4,5)-2,3,4,5-tetrahydroxycyclohexanemethanol 
• 105017-81-0 (1S,2S,3S,4R,5S)-5-(hydroxymethyl)cyclohexane-1,2,3,4-tetrol 

Relevant academic research and scientific papers

SYNTHESES OF PSEUDO-α-D-GLUCOPYRANOSE AND PSEUDO-β-L-IDOPYRANOSE, TWO OPTICALLY ACTIVE PSEUDO-HEXOPYRANOSES, FROM D-GLUCOSE BY USING STEREOSELECTIVE REDUCTIVE DEACETOXYLATION WITH SODIUM BOROHYDRIDE AND CYCLITOL FORMATION FROM NITROFURANOSE AS KEY REACTIO

Two optically active pseudo-hexopyranoses, pseudo-α-D-glucopyranose and pseudo-β-L-idopyranose, have been synthesized from D-glucose by using stereoselective deacetoxylations with NaBH4 and cyclitol formations from nitrofuranose derivatives as key reactio