193223-08-4

Upstream product

• 2595-07-5 allyl β-D-glucopyranoside 
• 2186-92-7 p-Anisaldehyde dimethyl acetal 
• 147649-92-1 allyl 4,6-O-(4-methoxybenzylidene)-β-D-glucopyranoside 
• 193222-97-8 [(2R,3R,4S,5R,6R)-6-Allyloxy-4,5-bis-(tert-butyl-dimethyl-silanyloxy)-3-(4-methoxy-benzyloxy)-tetrahydro-pyran-2-yl]-methanol 
• 10343-15-4 Acetic acid (2R,3R,4S,5R,6R)-3,5-diacetoxy-2-acetoxymethyl-6-allyloxy-tetrahydro-pyran-4-yl ester 
• 193223-12-0 (2S,3R,4S,5R,6R)-6-Allyloxy-4,5-bis-(tert-butyl-dimethyl-silanyloxy)-3-(4-methoxy-benzyloxy)-tetrahydro-pyran-2-carbaldehyde 

Downstream Products

• 193223-10-8 (2S,3R,4S,5R,6R)-6-Allyloxy-4,5-bis-(tert-butyl-dimethyl-silanyloxy)-3-(4-methoxy-benzyloxy)-tetrahydro-pyran-2-carboxylic acid amide 

Relevant academic research and scientific papers

A Moenomycin-type Structural Analogue of Lipid II Some Possible Mechanisms of the Mode of Action of Transglycosylase Inhibitors can be Discarded

The transglycosylation step in the peptidoglycan biosynthesis belongs to the general class of glycosyltransferase-catalyzed reactions. The structural analogue 2 of moenomycin A has been synthesized and has been found to be antibiotically inactive. The ass