863237-51-8

Upstream product

• 863237-60-9 1,5-Bis-benzyloxy-2-[3-(3,5-bis-benzyloxy-phenyl)-3-bromo-propyl]-3-methoxymethoxy-benzene 
• 863237-56-3 2,4-bis-benzyloxy-6-hydroxy-benzaldehyde 
• 487-70-7 2,4,6-trihydroxybenzaldehyde 
• 100-39-0 benzyl bromide 
• 108-73-6 3,5-dihydroxyphenol 
• 863237-58-5 3-(2,4-bis-benzyloxy-6-methoxymethoxy-phenyl)-1-(3,5-bis-benzyloxy-phenyl)-propan-1-one 
• 863237-49-4 3',4,5',6-tetrabenzyloxy-2-methoxymethyloxy-E-retro-chalcone 
• 863237-50-7 1-(3',5'-dibenzyloxyphenyl)-3-(2''-methoxymethyloxy-4'',6''-dibenzyloxyphenyl)propan-1-ol 
• 863237-41-6 4,6-dibenzyloxy-2-methoxymethyloxybenzaldehyde 
• 28924-21-2 3,5-dibenzyloxyacetophenone 

Downstream Products

• 863237-53-0 (1R,2R)-1-(3',5'-dibenzyloxyphenyl)-3-(2''-hydroxy-4'',6''-dibenzyloxyphenyl)propane-1,2-diol 
• 863237-52-9 (1R,2R)-1-(3',5'-dibenzyloxyphenyl)-3-(2''-methoxymethyloxy-4'',6''-dibenzyloxyphenyl)propane-1,2-diol 

Relevant academic research and scientific papers

Enantio selective synthesis of new phenylpropanoid: Isolated from Walsura trifoliata

A new phenylpropanoid containing flavon-3-ol has been isolated from the leaves of traditional medicinal plant, Walsura trifoliata. The structure of the compound was established on the basis of spectroscopic evidence [2D NMR, HREIMS] and by its alternative

Asymmetric total synthesis of B-ring modified (-)-epicatechin gallate analogues and their modulation of β-lactam resistance in Staphylococcus aureus

Two enantiomerically pure B-ring modified analogues of (-)-epicatechin gallate were synthesised and their modulation of β-lactam resistance using three strains of methicillin resistant Staphylococcus aureus (BB 568, EMRSA-15 and EMRSA-16) evaluated. Sub-i