110537-69-4

Upstream product

• 100-39-0 benzyl bromide 
• 82472-81-9 3',4':5,6-di-O-cyclohexylidene-tetra-N-methoxycarbonylneamine 

Downstream Products

• 66266-01-1 1,3-di-N-benzyl-5,6-O-cyclohexylidene-2-deoxy-1,3-di-N-methoxycarbonylstreptamine 
• 66266-02-2 1,3-di-N-benzyl-5,6-O-cyclohexylidene-2-deoxy-4-O-(2,3-dideoxy-α-D-erythro-hexopyranosyl)-1,3-di-N-methoxycarbonylstreptamine 
• 110537-79-6 1,3-di-N-benzyl-1,3-di-N-benzyloxycarbonyl-4-O-<6-benzyloxycarbonylamino-4-O-(6-benzyloxycarbonylamino-2,3,6-trideoxy-α-D-erythro-hexopyranosyl)-2,3,6-trideoxy-α-D-erythro-hexopyranosyl>-5,6-O-cyclohexylidene-2-deoxystreptamine 
• 110537-71-8 1,3-di-N-benzyl-4-O-<(1R,2R)-2-(N-benzylmethoxycarbonylamino)-1-<(1R)-2-(N-benzylmethoxycarbonylamino)-1-formylethoxy>-2-formylethyl>-5,6-O-cyclohexylidene-2-deoxy-1,3-di-N-methoxycarbonylstreptamine 
• 110537-72-9 1,3-di-N-benzyl-5,6-O-cyclohexylidene-2-deoxy-4-O-(4,6-di-O-acetyl-2,3-dideoxy-α-D-erythro-hex-2-enopyranosyl)-1,3-di-N-methoxycarbonylstreptamine 
• 110537-74-1 1,3-di-N-benzyl-5,6-O-cyclohexylidene-2-deoxy-4-O-(4,6-di-O-acetyl-2,3-dideoxy-α-D-erythro-hexopyranosyl)-1.3-di-N-methoxycarbonylstreptamine 
• 110537-73-0 1,3-di-N-benzyl-5,6-O-cyclohexylidene-2-deoxy-4-O-(2,3-dideoxy-α-D-erythro-hex-2-enopyranosyl)-1,3-di-N-methoxycarbonylstreptamine 
• 110611-75-1 4-O-<6-amino-4-O-(6-amino-2,3,6-trideoxy-α-D-erythro-hexopyranosyl)-2.3.6-trideoxy-α-D-erythro-hexopyranosyl>-2-deoxystreptamine tetrahydrochloride 
• 110537-77-4 4-O-(6-amino-2,3,6-trideoxy-α-D-erythro-hexopyranosyl)-1,3-di-N-benzyl-5,6-O-cyclohexylidene-2-deoxystreptamine 
• 73023-62-8 1L-N¹,N³-dibenzyl-N¹,O⁶-carbonyl-O⁴,O⁵-cyclohexane-1,1-diyl-N³-methoxycarbonyl-2-deoxy-streptamine 
• 110537-70-7 tetra-N-benzyl-5,6-O-cyclohexylidene-tetra-N-methoxycarbonylneamin 

Relevant academic research and scientific papers

SYNTHESIS OF APRAMYCIN ANALOGUES

The synthesis is described of a pseudotrisaccharide analogue of apramycin from a suitably protected 2-deoxystreptamine derivative by the stepwise application of the BF3-catalysed addition of alcohols to glycals.