74303-03-0

Upstream product

• 856438-60-3 4-(2-(benzyloxy)phenyl)-4-oxobutanal 
• 5896-17-3 2-(phenylmethoxy)benzaldehyde 
• 856438-50-1 2-(2-benzyloxy-phenyl)-2,5-dihydro-pyrrole-1-carboxylic acid methyl ester 
• 856438-58-9 1-(2-benzyloxy-phenyl)-pent-4-en-1-ol 
• 856438-59-0 1-(2-benzyloxy-phenyl)-pent-4-en-1-one 
• 856438-48-7 allyl-[1-(2-benzyloxy-phenyl)-3-trimethylsilanyl-prop-2-ynyl]-carbamic acid methyl ester 
• 856438-51-2 2-(2-benzyloxyphenyl)pyrrole-1-carboxylic acid methyl ester 
• 856438-49-8 allyl-[1-(2-benzyloxy-phenyl)-prop-2-ynyl]-carbamic acid methyl ester 

Downstream Products

• 42041-50-9 2-(2-hydroxyphenyl)-1H-pyrrole 
• 856438-54-5 2-(2-benzyloxy-phenyl)-1-ethyl-1H-pyrrole 
• 69640-32-0 2-(2-methoxyphenyl)pyrrole 
• 10245-83-7 3,4,5-Tribrom-2-(3',5'-dibrom-2'-methoxyphenyl)-1H-pyrrol 
• 10245-81-5 2,4-dibromo-6-(3,4,5-tribromo-1H-pyrrol-2-yl)phenol 

Relevant academic research and scientific papers

A re(V)-catalyzed C-N bond-forming route to human lipoxygenase inhibitors

(Chemical Equation Presented) A regioselective synthesis of propargylamines by the coupling of propargyl alcohols with tosylamines and carbamates catalyzed by an air-and moisture-tolerant rhenium-oxo complex is described. The ability to couple functionali

Aminopropanol derivatives of 2-(0-hydroxyphenyl)-pyrrole

Alkylaminopropanol derivatives of 2-(o-hydroxyphenyl)-pyrrole of the formula (I) STR1 where R is hydrogen or is alkyl of 1 to 8 carbon atoms which is unsubstituted or substituted by hydroxyl, alkoxy of 1 to 3 carbons atoms or cycloalkyl of 3 to 8 carbon a