724705-47-9

Upstream product

• 169736-18-9 (2S,3R,4S)-3,4-bis(benzyloxy)-2-[(benzyloxy)methyl]-5-methoxyoxolane 
• 13039-67-3 (2S,3S,4S)-2-(hydroxymethyl)-5-methoxyoxolane-3,4-diol 
• 106-95-6 allyl bromide 
• 160925-98-4 benzyl [(2R,3R,4R)-1,3,4-tris(benzyloxy)hex-5-en-2-yl]carbamate 
• 161290-44-4 (1R,2R,3R)-2,3-Bis-benzyloxy-1-benzyloxymethyl-pent-4-enylamine 
• 203112-67-8 2-[(2R,3R,4R)-1,3,4-tris(benzyloxy)hex-5-en-2-yl]isoindoline-1,3-dione 
• 41546-31-0 L-xylose 
• 137820-47-4 (3R,4R,5S)-5-hydroxy-3,4,6-tribenzyloxy-1-hexene 
• 366815-69-2 (3S,4R)-1,3,4-Tris-benzyloxy-hept-6-en-2-one 

Downstream Products

• 724705-50-4 (2R,3R,4R,5S,6S)-N-benzyloxycarbonyl-2-benzyloxymethyl-3,4-dibenzyloxy-5,6-dihydroxy-azepane 
• 724705-49-1 (2R,3R,4R,5R,6R)-N-benzyloxycarbonyl-2-benzyloxymethyl-3,4-dibenzyloxy-5,6-dihydroxy-azepane 
• 724705-48-0 (2R,3R,4R)-benzyl 3,4-bis(benzyloxy)-2-[(benzyloxy)methyl]-2,3,4,7-tetrahydro-1H-azepine-1-carboxylate 

Relevant academic research and scientific papers

Synthesis of d -Fagomine and Its Seven- and Eight-Membered Higher-Ring Analogues, and the Formal Synthesis of (+)-Australine from l -Xylose-Derived Chiron

The synthesis of d-fagomine and its seven- and eight-membered higher-ring analogues from commercially available l-xylose is reported. The syntheses involve elaboration of a common alkenol precursor obtained from l-xylose-derived hemiacetal. The key steps

The first synthesis of substituted azepanes mimicking monosaccharides: A new class of potent glycosidase inhibitors

The synthesis of the first examples of seven-membered ring iminoalditols, molecules displaying an extra hydroxymethyl substituent on their seven-membered ring compared to the previously reported polyhydroxylated azepanes, has been achieved from D-arabinos