77987-41-8

Upstream product

• 130155-18-9 phenyl 2,3-di-O-acetyl-4-O-(2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl)-6-deoxy-1-thio-β-D-xylo-hexo-5-enopyranoside 
• 77987-40-7 methyl 2,3-di-O-acetyl-4-O-(2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl)-6-deoxy-β-D-xylo-hex-5-enopyranoside 
• 130130-53-9 phenyl 2,3-di-O-acetyl-4-O-(2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl)-6-O-(p-tolylsulphonyl)-1-thio-β-D-glucopyranoside 
• 130130-52-8 phenyl 2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl-(1→4)-2,3,6-tri-O-acetyl-1-thio-β-D-glucopyranoside 
• 130130-54-0 Acetic acid (2S,3R,4S,5S,6S)-3-acetoxy-6-iodomethyl-2-phenylsulfanyl-5-((2R,3R,4S,5R,6R)-3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-4-yl ester 
• 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 
• 25787-32-0 methyl 6-deoxy-2,2',3,3',4',6'-hexa-O-acetyl-6-iodo-β-maltoside 

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

Partial Conversion of Maltose into Cyclohexane Derivatives

5,6-Unsaturated disaccharide derivative prepared from maltose via its 6-iodo derivative was treated with mercuric chloride, giving α-linked pseudodisaccharide in good yield, which contains cyclohexanone derivatives as constituents.On treatment with an ace