196876-49-0

Upstream product

• 16758-34-2 1-thiophenyl-β-D-galactopyranoside 
• 196876-47-8 phenyl 3-O-benzyl-1-thio-β-D-galactopyranoside 
• 100-39-0 benzyl bromide 
• 98-88-4 benzoyl chloride 
• 124477-08-3 phenyl 3-O-benzyl-4,6-O-benzylidene-1-thio-β-D-galactopyranoside 

Downstream Products

• 725228-84-2 phenyl 2-O-benzoyl-3-O-benzyl-1-thio-β-D-galactopyranoside 
• 936324-87-7 phenyl 2-O-benzoyl-3-O-benzyl-4,6-O-[1-(R)-(methoxycarbonyl)-ethylidene]-1-thio-β-D-galactopyranoside 
• 936324-88-8 C₂₇H₃₂O₉ 
• 936324-90-2 isopropyl 2-O-benzoyl-3-O-[2-azido-4,6-O-benzylidene-3-O-(2,3,5,6-tetra-O-benzoyl-β-D-galactofuranosyl)-2-deoxy-α-D-galactopyranosyl]-4,6-O-[1-(R)-(methoxycarbonyl)-ethylidene]-β-D-galactopyranoside 
• 936324-92-4 isopropyl 2,3,5,6-tetra-O-benzoyl-β-D-galactofuranosyl-(1->3)-2-azido-6-O-benzyl-2-deoxy-α-D-galactopyranosyl-(1->3)-2-O-benzoyl-4,6-O-[1-(R)-(methoxycarbonyl)-ethylidene]-β-D-galactopyranoside 
• 936324-85-5 isopropyl 2-O-benzoyl-4,6-O-[1-(R)-(methoxycarbonyl)-ethylidene]-β-D-galactopyranoside 
• 1441127-90-7 2-(trimethylsilyl)ethyl 2-O-benzoyl-3-O-benzyl-4,6-O-benzylidene-β-D-galactopyranoside 
• 1441128-08-0 2-(trimethylsilyl)ethyl (2-O-benzyl-4,6-O-benzylidene-α-D-galactopyranosyl)-(1→4)-2-O-benzoyl-3,6-di-O-benzyl-β-D-galactopyranoside 
• 1441127-99-6 2-(trimethylsilyl)ethyl (2-O-benzyl-4,6-O-benzylidene-3-O-chloroacetyl-α-D-galactopyranosyl)-(1→4)-2-O-benzoyl-3,6-di-O-benzyl-β-D-galactopyranoside 
• 1441128-04-6 2-(trimethylsilyl)ethyl (2-O-benzyl-4,6-O-benzylidene-3-O-chloroacetyl-β-D-galactopyranosyl)-(1→4)-2-O-benzoyl-3,6-di-O-benzyl-β-D-galactopyranoside 
• 117253-09-5 2-(trimethylsilyl)ethyl 2-O-benzoyl-3,6-di-O-benzyl-β-D-galactopyranoside 
• 1163124-32-0 phenyl 2-O-benzoyl-3,6-di-O-benzyl-1-thio-β-D-galactopyranoside 
• 917568-59-3 phenyl [2-(trimethylsilyl)ethyl 3,4-di-O-benzyl-2-O-benzoyl-β-D-galactopyrosyluronate]-(1->4)-2-deoxy-2-tetrachlorophthalimido-1-thio-β-D-glucopyranoside 
• 917568-60-6 phenyl [2-(trimethylsilyl)ethyl 3,4-di-O-benzyl-2-O-benzoyl-β-D-galactopyrosyluronate]-(1->4)-2-deoxy-2-tetrachlorophthalimido-1-thio-β-D-glucopyranoside S-oxide 

Relevant academic research and scientific papers

The total synthesis of moenomycin A

Moenomycin A is the only known natural antibiotic that inhibits bacterial cell wall synthesis by binding to the transglycosylases that catalyze formation of the carbohydrate chains of peptidoglycan. We report here the total synthesis of moenomycin A using