860795-52-4

Upstream product

• 100-39-0 benzyl bromide 
• 860795-44-4 6-O-benzoyl-3',4'-di-O-benzyl-1-N-tert-butoxycarbonyl-3,2',3'-triazidoneamine 
• 485809-80-1 4-azido-2,3-di-O-acetyl-4,6-dideoxy-α-D-glucopyranosyl trichloroacetimidate 
• 860795-33-1 3',4'-di-O-benzyl-5,6-di-O-(p-chlorobenzoyl)-1,3,2',3'-tetraazidoneamine 
• 688744-65-2 1,3,2’,6’-tetrazido-5,6-O-cyclohexylidene neamine 
• 549501-27-1 3′,4′-di-O-benzyl-1,3,2′,6′-tetraazidoneamine 

Downstream Products

• 860795-53-5 5-O-(4-azido-3,6-dideoxy-β-D-glucopyranosyl)-3',4'-di-O-benzyl-1-N-[(S)-4-(benzyloxycarbonylamino)-2-hydroxybutanoyl]-3,2',3'-triazidoneamine 

Relevant academic research and scientific papers

Novel anti bacterial compounds

The invention relates to novel paranmycin compounds that have activity against gram positive and gram negative bacteria, preferably bacteria that are resistant to other antibiotics. Paranmycins are of the general formula

Tuning the regioselectivity of the staudinger reaction for the facile synthesis of kanamycin and neomycin class antibiotics with N-1 modification

(Chemical Equation Presented) A novel method for achieving the desired regioselective reduction of the N-1 azido group on a tetraazidoneamine has been developed that leads to the synthesis of both kanamycin and neomycin class antibiotics bearing N-1 modif