236115-80-3

Upstream product

• 236115-79-0 hexaazido-hepta-O-benzyl neomycin 
• 67-56-1 methanol 

Downstream Products

• 236115-81-4 5-O-allyl-1,3,2',6'-tetraazido-6,3',4'-tri-O-benzyl neamine 
• 477329-90-1 Acetic acid (2S,3R,4R,5S,6S)-4,5-diacetoxy-2-[(1R,2R,3S,5R,6S)-3,5-diazido-2-((2R,3R,4R,5R,6R)-3-azido-6-azidomethyl-4,5-bis-benzyloxy-tetrahydro-pyran-2-yloxy)-6-benzyloxy-cyclohexyloxy]-6-methyl-tetrahydro-pyran-3-yl ester 
• 477329-92-3 Acetic acid (2S,3S,4R,5S,6S)-4,5-diacetoxy-6-acetoxymethyl-2-[(1R,2R,3S,5R,6S)-3,5-diazido-2-((2R,3R,4R,5R,6R)-3-azido-6-azidomethyl-4,5-bis-benzyloxy-tetrahydro-pyran-2-yloxy)-6-benzyloxy-cyclohexyloxy]-tetrahydro-pyran-3-yl ester 
• 477329-91-2 Acetic acid (2S,3R,4S,5R,6S)-5-acetoxy-6-azidomethyl-4-benzyloxy-2-[(1R,2R,3S,5R,6S)-3,5-diazido-2-((2R,3R,4R,5R,6R)-3-azido-6-azidomethyl-4,5-bis-benzyloxy-tetrahydro-pyran-2-yloxy)-6-benzyloxy-cyclohexyloxy]-tetrahydro-pyran-3-yl ester 
• 502621-26-3 Acetic acid (2S,3R,4S,5R,6R)-5-acetoxy-4-(2-azido-ethoxy)-2-[(1R,2R,3S,5R,6S)-3,5-diazido-2-((2R,3R,4R,5R,6R)-3-azido-6-azidomethyl-4,5-bis-benzyloxy-tetrahydro-pyran-2-yloxy)-6-benzyloxy-cyclohexyloxy]-6-methyl-tetrahydro-pyran-3-yl ester 
• 502621-23-0 Acetic acid (2S,3R,4S,5R,6R)-4-(2-acetoxy-ethoxy)-5-azido-2-[(1R,2R,3S,5R,6S)-3,5-diazido-2-((2R,3R,4R,5R,6R)-3-azido-6-azidomethyl-4,5-bis-benzyloxy-tetrahydro-pyran-2-yloxy)-6-benzyloxy-cyclohexyloxy]-6-methyl-tetrahydro-pyran-3-yl ester 
• 502621-25-2 Acetic acid (2S,3R,4S,5R,6R)-5-acetoxy-4-(2-acetoxy-ethoxy)-2-[(1R,2R,3S,5R,6S)-3,5-diazido-2-((2R,3R,4R,5R,6R)-3-azido-6-azidomethyl-4,5-bis-benzyloxy-tetrahydro-pyran-2-yloxy)-6-benzyloxy-cyclohexyloxy]-6-methyl-tetrahydro-pyran-3-yl ester 
• 502621-22-9 Acetic acid (2S,3R,4S,5R,6R)-4-acetoxy-5-(2-acetoxy-ethoxy)-2-[(1R,2R,3S,5R,6S)-3,5-diazido-2-((2R,3R,4R,5R,6R)-3-azido-6-azidomethyl-4,5-bis-benzyloxy-tetrahydro-pyran-2-yloxy)-6-benzyloxy-cyclohexyloxy]-6-methyl-tetrahydro-pyran-3-yl ester 
• 502621-24-1 Acetic acid (2S,3R,4S,5R,6R)-5-acetoxy-4-(2-acetoxy-ethoxy)-6-acetoxymethyl-2-[(1R,2R,3S,5R,6S)-3,5-diazido-2-((2R,3R,4R,5R,6R)-3-azido-6-azidomethyl-4,5-bis-benzyloxy-tetrahydro-pyran-2-yloxy)-6-benzyloxy-cyclohexyloxy]-tetrahydro-pyran-3-yl ester 
• 675616-55-4 5-O-(2,4-di-O-acetyl-3-O-allyl-6-deoxy-β-D-glucopyranosyl)-6,3',4'-tri-O-benzyl-1,3,2',6'-tetraazidoneamine 
• 675616-59-8 5-O-(2,3,4-tri-O-acetyl-6-deoxy-6-fluoro-β-D-glucopyranosyl)-6,3',4'-tri-O-benzyl-1,3,2',6'-tetraazidoneamine 
• 285994-43-6 (2R,3R,4R,5R,6R)-3-Azido-6-azidomethyl-4,5-bis-benzyloxy-2-[(1R,2R,3S,4R,6S)-4,6-diazido-3-benzyloxy-2-((R)-1-oxiranylmethoxy)-cyclohexyloxy]-tetrahydro-pyran 
• 1432025-32-5 C₂₁H₃₇N₇O₇ 
• 1432025-33-6 C₂₀H₃₆N₈O₆ 

Relevant academic research and scientific papers

Reexamination of neomycin B degradation: Efficient preparation of its CD and D rings as protected glycosyl donors

(matrix presented) The degradation of neomycin B was reexamined, and a novel protocol was established to prepare the properly masked neomycin CD ring as a glycol donor in excellent yield. Glycosylation of the CD ring with glycol acceptors provided a facil

The chemistry of amine-azide interconversion: Catalytic diazotransfer and regioselective azide reduction

Azides have proven to be useful precursors to amines in organic syntheses. This report describes an improvement of the diazotransfer reaction and the first example of a regioselective azide reduction of compounds containing multiple azides. The use of a s

Design and synthesis of new aminoglycoside antibiotics containing neamine as an optimal core structure: Correlation of antibiotic activity with in vitro inhibition of translation

The structure and activity of the pseudodisaccharide core found in aminoglycoside antibiotics was probed with a series of synthetic analogues in which the position of amino groups was varied around the glucopyranose ring. The naturally occurring structure