77994-68-4

Upstream product

• 98-59-9 p-toluenesulfonyl chloride 
• 37669-00-4 1,2-O-isopropylidene-β-D-threofuranose 
• 77994-68-4 1,2-O-isopropylidene-3-O-p-toluenesulfonyl-β-D-threofuranose 
• 76778-02-4 3-O-benzoyl-1,2-O-isopropylidene-α-L-erythrofuranose 
• 76821-48-2 1,2-O-isopropylidene-α-L-erythrofuranose 

Downstream Products

• 76778-02-4 3-O-benzoyl-1,2-O-isopropylidene-α-L-erythrofuranose 
• 22894-00-4 3-deoxy-3-(2-hydroxybenzylideneamino)-1,2-O-isopropylidene-α-L-erythrofuranose 
• 77994-71-9 3-deoxy-1,2-O-isopropylidene-3-(4-methoxybenzylideneamino)-α-L-erythrofuranose 
• 77994-72-0 3-benzamido-3-deoxy-1,2-O-isopropylidene-α-L-erythrofuranose 
• 78039-20-0 3-benzamido-3-deoxy-1,2-O-isopropylidene-β-D-threofuranose 
• 76778-02-4 3-O-Benzoyl-1,2-O-isopropylidene-β-D-threofuranose 
• 77994-68-4 1,2-O-isopropylidene-3-O-p-toluenesulfonyl-α-L-erythrofuranose 

Relevant academic research and scientific papers

THE PREPARATION OF 3-AMINO-3-DEOXY-1,2-ISOPROPYLIDENE-α-L-ERYTHROFURANOSE, 3-AMINO-3-DEOXY-1,2-O-ISOPROPYLIDENE-β-D-THREOFURANOSE AND THEIR DERIVATIVES

The title amino derivatives VI and XIV were prepared by nucleophilic substitution of p-toluenesulfonyl derivatives II and XVII with sodium azide or hydrazine and subsequent reduction.Nucleophilic substitution of compounds II and XVII with sodium benzoate