220827-29-2

Upstream product

• 126214-82-2 1,2-O-isopropyliden-5-O-allyl-α-D-glucofuranosidurono-6,3-lactone 
• 156325-49-4 1,2-O-isopropyliden-5-O-allyl-α-D-glucofuranosiduronamide 
• 3067-56-9 D-glucurono-3,6-lactone acetonide 
• 220827-22-5 1,2-O-isopropyliden-5-O-allyl-3-O-phenoxycarbonyl-α-D-glucofuranosiduronamide 
• 161545-19-3 3,4,6-tri-O-acetyl-2-deoxy-2-trichloroacetamido-α/β-D-glucopyranose trichloroacetimidate 
• 220827-24-7 allyl 5-O-allyl-3-O-phenoxycarbonyl-β-D-glucofuranosiduronamide 

Downstream Products

• 220827-30-5 Allyl 2-O-(2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranosyl)-5-O-allyl-3-O-phenoxycarbonyl-β-D-glucofuranosiduronamide 

Relevant academic research and scientific papers

Moenomycin A: The role of the methyl group in the moenuronamide unit and a general discussion of structure-activity relationships

Two disaccharide analogues lb and 17a of moenomycin A have been synthesized and their antibiotic and transglycosylase-inhibiting properties have been determined. The results permit for the first time to arrive at a general view of the structural requirements in this class of compounds necessary to elicit antibiotic activity.