122777-35-9

Upstream product

• 108-24-7 acetic anhydride 
• 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 
• 118068-40-9 (3S,4R,5S,6S)-4,5-Bis-benzyloxy-6-methoxy-2-methylene-tetrahydro-pyran-3-ol 
• 118068-41-0 2,3-di-O-benzyl-6-deoxy-D-arabino-5-hexulofuranose 
• 118068-39-6 methyl 2,3-di-O-benzyl-6-deoxy-6-iodo-α-D-altropyranoside 
• 66537-92-6 methyl 2,3-anhydro-4,6-benzylidene-α-D-allopyranoside 
• 118068-45-4 2-hydroxy-4-methylphenyl 6'-deoxy-β-D-arabino-5'-hexulofuranoside 
• 118068-43-2 4-((3S,4S,5S)-5-Acetyl-3,4-bis-benzyloxy-tetrahydro-furan-2-yloxy)-3-benzyloxy-benzaldehyde 
• 99212-27-8 methyl 4,6-O-benzylidene-2,3-di-O-benzyl-α-D-altropyranoside 
• 33164-03-3 methyl 2,3-di-O-benzyl-α-D-altropyranoside 
• 118068-47-6 2-acetoxy-4-methylphenyl 2',3'-di-O-acetyl-6'-deoxy-β-D-arabino-5'-hexulofuranoside 
• 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 

Downstream Products

• 129141-65-7 Acetic acid (2S,3S,4S,5S)-4-acetoxy-5-{2-acetoxy-4-[(E)-2-((1R,2S,3R,4S,5S,6R)-2,3,5,6-tetraacetoxy-4-methoxy-cyclohexylcarbamoyl)-propenyl]-phenoxy}-2-(2-methyl-[1,3]dioxolan-2-yl)-tetrahydro-furan-3-yl ester 
• 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 
• 75081-92-4 hygromycin A 

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

Total Synthesis of Hygromycin A

The first complete synthesis of antibiotic hygromycin A is reported; coupling of the protected sugar moiety (2) and the aminocyclitol (3) derived from D-glucose as the optically active form, followed by deprotection, gives the product (1) which was identi