134308-73-9

Upstream product

• 121195-21-9 methyl 3,5-di-O-benzyl-2,6-dideoxy-2,6-imino-D-mannofuranoside 
• 501-53-1 benzyl chloroformate 
• 121250-70-2 methyl 3,5-di-O-benzyl-N-benzyloxycarbonyl-2,6-dideoxy-2,6-imino-α-D-mannofuranoside 
• 121195-22-0 methyl 3,5-di-O-benzyl-N-benzyloxycarbonyl-2,6-dideoxy-2,6-imino-D-mannofuranoside 

Downstream Products

• 14199-63-4 1-deoxymannojirimycin 
• 113000-77-4 (2S,3R,4R,5R)-3,4,5-trihydroxypipecolic acid 
• 121195-28-6 3,5-di-O-benzyl-N-benzyloxycarbonyl-2,6-dideoxy-2,6-imino-D-mannono-1,4-lactone 
• 121195-23-1 (2S,3R,4R,5R)-3,5-Bis-benzyloxy-4-hydroxy-piperidine-1,2-dicarboxylic acid 1-benzyl ester 
• 121195-27-5 2,4-di-O-benzyl-N-benzyloxycarbonyl-1,5-dideoxy-1,5-imino-D-mannitol 

Relevant academic research and scientific papers

A PRACTICAL SYNTHESIS OF DEOXYMANNOJIRIMYCIN AND OF (2S,3R,4R,5R)-3,4,5-TRIHYDROXYPIPECOLIC ACID FROM D-GLUCOSE

Deoxymannojirimycin may be prepared in moderate amounts in an overall yield of 35percent in ten steps from diacetone glucose; the key step is formation of the piperidine ring by intramolecular nucleophilic displacement of a triflate at C-2 of a methyl glucofuranoside by a nitrogen function at C-6, irrespective of the anomeric configuration of the sugar.A synthesis of (2S,3R,4R,5R)-3,4,5-trihydroxypipecolic acid is reported.