110403-83-3

Upstream product

• 114048-03-2 1,6-anhydro-4-O-(2-azido-4,6-O-benzylidene-2-deoxy-α-D-allopyranosyl)-3-O-benzyl-2-O-(p-methoxybenzyl)-β-D-glucopyranose 
• 77-76-9 2,2-dimethoxy-propane 
• 824-94-2 p-methoxybenzyl chloride 
• 28868-67-9 2,3-di-O-acetyl-1,6-anhydro-4-O-(2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl)-β-D-glycopyranose 
• 130130-44-8 1,6-anhydro-2,3-di-O-benzoyl-4',6'-O-benzylidene-2',3'-di-O-methylsulphonyl-β-maltose 
• 130130-43-7 1,6-anhydro-2,3-di-O-benzoyl-4',6'-O-benzylidene-2',3'-O-(1,1,3,3-tetraisopropyldisiloxane-1,3-diyl)-β-maltose 
• 6983-27-3 1,6-anhydro-β-maltose 
• 114048-00-9 1,6-anhydro-3-O-benzyl-4',6'-O-benzylidene-2',3'-di-O-methylsulphonyl-2-O-pivaloyl-β-maltose 
• 114047-99-3 1,6-anhydro-4',6'-O-benzylidene-2',3'-di-O-methylsulphonyl-2-O-pivaloyl-β-maltose 
• 114048-02-1 1,6-anhydro-4-O-(2,3-anhydro-4,6-O-benzylidene-α-D-allopyranosyl)-3-O-benzyl-2-O-(p-methoxybenzyl)-β-D-glucopyranose 
• 114129-74-7 1,6-anhydro-4',6'-O-benzylidene-2',3'-O-(1,1,3,3-tetraisopropyldisiloxane-1,3-diyl)-β-maltose 
• 114048-01-0 1,6-anhydro-4-O-(2,3-anhydro-4,6-O-benzylidene-α-D-allopyranosyl)-3-O-benzyl-β-D-glucopyranose 
• 130130-45-9 1,6-anhydro-4-O-(2-azido-4,6-O-benzylidene-2-deoxy-α-D-altropyranosyl)-3-O-benzyl-2-O-(p-methoxybenzyl)-β-D-glucopyranose 

Downstream Products

• 110424-94-7 1,6-anhydro-3-O-benzyl-4-O-<2,6-diazido-2,6-dideoxy-3,4-O-isopropylidene-α-D-allopyranosyl>-2-O-(p-methoxybenzyl)-β-D-glucopyranose 
• 110403-97-9 Methanesulfonic acid (3aS,4R,6R,7R,7aS)-7-azido-6-[(1R,2R,3S,4R,5R)-3-benzyloxy-4-(4-methoxy-benzyloxy)-6,8-dioxa-bicyclo[3.2.1]oct-2-yloxy]-2,2-dimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-4-ylmethyl ester 

Relevant academic research and scientific papers

Design and Synthesis of New 1,4-Diaminocyclitol Aminoglycosides: Use of Maltose as the Key Starting Material

New antimicrobial aminoglycosides having a pseudodisaccharide structure, 1L-(1,6/2,3)-3-amino-2-(2,6-diamino-2,6-dideoxy-α-D-allopyranosyloxy)-6-(glycyl(methyl)amino)cyclohexanol (4) and its 3'-deoxy analogue (5) have been synthesized from 1,6-anhydro-β-m

SYNTHESIS OF A NEW ANTIMICROBIAL AMINOGLYCOSIDE EMPLOYING MALTOSE AS A KEY STARTING MATERIAL

Maltose was chemically converted to a new 1,4-diaminocyclitol aminoglycoside (2) with moderate antimicrobial activities, developing several novel synthetic methodology.