118068-40-9

Upstream product

• 100-44-7 benzyl chloride 
• 66537-92-6 methyl 2,3-anhydro-4,6-benzylidene-α-D-allopyranoside 
• 99212-27-8 methyl 4,6-O-benzylidene-2,3-di-O-benzyl-α-D-altropyranoside 
• 33164-02-2 Methyl-2.3-di-O-benzyl-4.6-O-benzyliden-α-D-altropyranosid 
• 33164-03-3 methyl 2,3-di-O-benzyl-α-D-altropyranoside 
• 3150-15-0 methyl 2,3-anhydro-4,6-O-benzylidene-α-D-allopyranoside 
• 118068-39-6 methyl 2,3-di-O-benzyl-6-deoxy-6-iodo-α-D-altropyranoside 

Downstream Products

• 122777-43-9 Acetic acid (2S,3S,4S,5S)-4-acetoxy-5-{2-acetoxy-4-[(E)-2-((3aS,4R,5S,6S,7R,7aS)-4,6,7-triacetoxy-hexahydro-benzo[1,3]dioxol-5-ylcarbamoyl)-propenyl]-phenoxy}-2-(2-methyl-[1,3]dioxolan-2-yl)-tetrahydro-furan-3-yl ester 
• 127213-11-0 hygromycin A ethylene acetal 
• 127213-10-9 2-acetoxy-4-<(E)-2-(ethoxycarbonyl)-1-propen-1-yl>phenyl 2',3'-di-O-acetyl-6'-deoxy-β-D-arabino-5'-hexulofuranoside ethylene acetal 
• 122777-42-8 2-acetoxy-4-formylphenyl 2',3'-di-O-acetyl-6'-deoxy-β-D-arabino-5'-hexulofuranoside ethylene acetal 
• 127213-09-6 2-acetoxy-4-methylphenyl 2',3'-di-O-acetyl-6'-deoxy-β-D-arabino-5'-hexulofuranoside ethylene acetal 
• 122777-35-9 2-acetoxy-4-<(E)-2-carboxy-1-propen-1-yl>phenyl 2',3'-di-O-acetyl-6'-deoxy-β-D-arabino-5'-hexulofuranoside ethylene acetal 
• 75081-92-4 hygromycin A 
• 118068-48-7 2-acetoxy-4-formylphenyl 2',3'-di-O-acetyl-6'-deoxy-α-D-arabino-5'-hexulofuranoside 
• 118068-48-7 2-acetoxy-4-formylphenyl 2',3'-di-O-acetyl-6'-deoxy-β-D-arabino-5'-hexulofuranoside 
• 118068-47-6 2-acetoxy-4-methylphenyl 2',3'-di-O-acetyl-6'-deoxy-α-D-arabino-5'-hexulofuranoside 
• 118068-47-6 2-acetoxy-4-methylphenyl 2',3'-di-O-acetyl-6'-deoxy-β-D-arabino-5'-hexulofuranoside 
• 118068-45-4 2-hydroxy-4-methylphenyl 6'-deoxy-β-D-arabino-5'-hexulofuranoside 
• 118068-45-4 2-hydroxy-4-methylphenyl 6'-deoxy-α-D-arabino-5'-hexulofuranoside 
• 118068-43-2 4-((3S,4S,5S)-5-Acetyl-3,4-bis-benzyloxy-tetrahydro-furan-2-yloxy)-3-benzyloxy-benzaldehyde 

Relevant academic research and scientific papers

Total Synthesis of Antibiotic Hygromycin A

The first total synthesis of the antibiotic (-)-hygromycin A (1) has been achieved by a coupling reaction of the sugar moiety (2) and the cyclitol moiety (3).Both components were synthesized in homochiral forms starting from D-glucose.This synthesis fully

Synthesis of 2-Acetoxy-4-formylphenyl 2,3-Di-O-acetyl-6-deoxy-β-D-arabino-5-hexulofuranoside, Structure Confirmation of the Anomeric Configuration of Antibiotic Hygromycin A

2-Acetoxy-4-formylphenyl 2,3-di-O-acetyl-6-deoxy-β-D-arabino-5-hexulofuranoside, one of the degradation products of antibiotic hygromycin A, was synthesized.The present study confirmed the anomeric configuration of the antibiotic to be "β".