85464-60-4

Upstream product

• 108-24-7 acetic anhydride 
• 933-40-4 cycloxexanone dimethyl ketal 
• 60076-41-7 methyl 4,6-O-benzylidene-2-(benzyloxycarbonyl)amino-2-deoxy-α-D-glucopyranoside 
• 3068-36-8 3,4,6-tri-O-acetyl-2-deoxy-2-(2,4-dinitroanilino)-α-D-glucopyranosyl bromide 
• 100-52-7 benzaldehyde 
• 85464-56-8 Acetic acid (2R,3S,4R,5R,6S)-3-acetoxy-2-acetoxymethyl-6-{(2S,3R,4R,5S,6R)-3-benzyloxycarbonylamino-5-hydroxy-2-methoxy-6-[(4-methoxy-phenyl)-diphenyl-methoxymethyl]-tetrahydro-pyran-4-yloxy}-5-(2,4-dinitro-phenylamino)-tetrahydro-pyran-4-yl ester 
• 85464-57-9 Acetic acid (2R,3S,4R,5R,6S)-5-benzyloxycarbonylamino-4-((2S,3R,4R,5S,6R)-4,5-diacetoxy-6-acetoxymethyl-3-benzyloxycarbonylamino-tetrahydro-pyran-2-yloxy)-6-methoxy-2-[(4-methoxy-phenyl)-diphenyl-methoxymethyl]-tetrahydro-pyran-3-yl ester 
• 85502-93-8 [(2S,3R,4R,5S,6R)-2-((1R,2S,3S,4R,5S,6R)-2-Benzyloxycarbonylamino-3,5,6-trihydroxy-4-nitro-cyclohexyloxy)-4,5-dihydroxy-6-hydroxymethyl-tetrahydro-pyran-3-yl]-carbamic acid benzyl ester 
• 85464-55-7 Acetic acid (2R,3S,4R,5R,6S)-3-acetoxy-2-acetoxymethyl-6-((4aR,6S,7R,8R,8aS)-7-benzyloxycarbonylamino-6-methoxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-8-yloxy)-5-(2,4-dinitro-phenylamino)-tetrahydro-pyran-4-yl ester 
• 85502-91-6 Acetic acid (2R,3S,4R,5R,6S)-3-acetoxy-2-acetoxymethyl-6-((2S,3R,4R,5S,6R)-3-benzyloxycarbonylamino-5-hydroxy-6-hydroxymethyl-2-methoxy-tetrahydro-pyran-4-yloxy)-5-(2,4-dinitro-phenylamino)-tetrahydro-pyran-4-yl ester 
• 85464-58-0 Acetic acid (3S,4R,5R,6S)-2-acetoxy-5-benzyloxycarbonylamino-4-((2S,3R,4R,5S,6R)-4,5-diacetoxy-6-acetoxymethyl-3-benzyloxycarbonylamino-tetrahydro-pyran-2-yloxy)-6-methoxy-tetrahydro-pyran-3-yl ester 
• 85464-59-1 [(4aR,6S,7R,8R,8aS)-6-((1R,2S,3S,4R,5S,6R)-2-Benzyloxycarbonylamino-3,5,6-trihydroxy-4-nitro-cyclohexyloxy)-8-hydroxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yl]-carbamic acid benzyl ester 

Downstream Products

• 85464-61-5 C₄₁H₄₇N₃O₁₃ 
• 23600-10-4 [(1R,2S,3R,4R,5S)-5-Benzyloxycarbonylamino-4-((2S,3R,4R,5S,6R)-3-benzyloxycarbonylamino-4,5-dihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-yloxy)-2,3-dihydroxy-cyclohexyl]-carbamic acid benzyl ester 

Relevant academic research and scientific papers

A NEW SYNTHETIC APPROACH TO AMINOGLYCOSIDE ANTIBIOTICS BY USE OF OXIDATIVE DECARBOXYLATION AND REDUCTIVE DEACETOXYLATION AS KEY-REACTIONS

By use of a decarboxylation reaction with lead tetraacetate and a deacetoxylation reaction with sodium borohydride as key-reactions, paromamine (12) and tri-N-benzyloxycarbonylparomamine (12a) were synthesized from D-glucosamine.