6216-32-6

Upstream product

• 14429-30-2 2-Desoxy-streptamin-dihydrochlorid 
• 501-53-1 benzyl chloroformate 
• 2037-48-1 2-deoxystreptamine 
• 6216-31-5 2-deoxystreptamine pentaacetate 
• 13139-17-8 N-(Benzyloxycarbonyloxy)succinimide 
• 2037-48-1 (1α,2α,3α,4β,6β)-4,6-Diamino-1,2,3-cyclohexantriol 

Downstream Products

• 6471-56-3 4,5,6-Tri-O-acetyl-1,3-bis-N-(benzyloxycarbonyl)-2-desoxystreptamin 
• 74342-39-5 1,3-Di-N-benzyl-6-O-benzyl-3,4-N,O-carbonyl-2-desoxystreptamin 
• 74342-41-9 1,3-Di-N-benzyl-5,6-di-O-benzyl-3,4-N,O-carbonyl-2-desoxystreptamin 
• 64951-82-2 1,3-Bis-N-(benzyloxycarbonyl)-4,6-di-O-mesyl-2-desoxystreptamin 
• 74342-31-7 1,3-Bis-N-(benzyloxycarbonyl)-4,5-di-O-mesyl-2-desoxystreptamin 
• 74342-30-6 1,3-Bis-N-(benzyloxycarbonyl)-6-O-mesyl-2-desoxystreptamin 
• 74342-28-2 1,3-Bis-N-(benzyloxycarbonyl)-4,5,6-tri-O-mesyl-2-desoxystreptamin 
• 103813-98-5 (3aR,4aS,7aR,8R,8aS)-8-((2S,3S,4S,5S,6R)-6-Benzyloxymethyl-3,4,5-trihydroxy-tetrahydro-pyran-2-yloxy)-3,5-dimethyl-hexahydro-benzo[1,2-d;5,4-d']bisoxazole-2,6-dione 
• 101703-46-2 1-N,6-O:3-N,4-O-dicarbonyl-1,3-di-N-methyl-5-O-(2,3,4-tri-O-allyl-6-O-benzyl-β-D-mannopyranosyl)-2-deoxystreptamine 
• 101703-47-3 5-O-(6-O-benzyl-2,3,4-tris-O-trimethylsilyl-β-D-mannopyranosyl)-1-N,6-O:3-N,4-O-dicarbonyl-1,3-di-N-methyl-2-deoxystreptemine 
• 103813-95-2 C₆₀H₇₇N₃O₁₃ 
• 103813-96-3 5-O-<6-O-benzyl-2,3-O-<6-deoxy-6-ethoxycarbonylamino-2,3,4,7-tetra-O-(p-methylbenzyl)-L-glycero-D-galacto-(R)-heptopyranosylidene>-β-D-mannopyranosyl>-1-N,6O:3-N,4-O-dicarbonyl-1,3-di-N-methyl-2-deoxystreptamine 
• 103813-96-3 5-O-<6-O-benzyl-2,3-O-<6-deoxy-6-ethoxycarbonylamino-2,3,4,7-tetra-O-(p-methylbenzyl)-L-glycero-D-galacto-(R)-heptopyranosylidene>-β-D-talopyranosyl>-1-N,6-O:3-N,4-O-dicarbonyl-1,3-di-N-methyl-2-deoxystreptamine 
• 103813-97-4 C₆₈H₈₅N₃O₁₇Si 

Relevant academic research and scientific papers

SYNTHESIS OF DESTOMYCIN C, A PSEUDO-TRISACCHARIDE ANTIBIOTIC HAVING AN INTERGLYCOSIDIC SPIRO-ORTHOESTER LINKAGE

Destomycin C, a pseudo-trisaccharide antibiotic of orthosomycin family was synthesized via spiro-orthoester formation between 5-O-(β-D-mannopyranosyl)-2-deoxystreptamine and 6-amino-6-deoxyheptonolactone derivatives.

CONTROL OF SITE-SPECIFIC SUBSTITUTION OF AMINOGLYCOSIDES BY TRANSITION METAL CATIONS

The site of transistion metal-directed acylations of apramycin and related aminoglycosides can be altered simply by changing the metal cation employed in the reaction.