93424-89-6

Upstream product

• 93424-83-0 3-hydroxy-7-methoxy-4-phenyl-4H-furo<3,2-b>indole-2-carboxylic acid methyl ester 
• 89224-53-3 3-hydroxy-7-methoxy-4-phenyl-4H-furo<3,2-b>indole-2-carboxylic acid methyl ester 
• 89224-79-3 5-methoxy-2-<(2-methoxy-2-oxoethyl)phenylamino>benzoic acid methyl ester 
• 89224-52-2 5-methoxy-3-(2-methoxy-2-oxoethoxy)-1-phenyl-1H-indole-2-carboxylic acid methyl ester 
• 89224-77-1 2-[(Cyanomethyl)phenylamino]-5-methoxy-benzoic acid 
• 89224-78-2 2-<(carboxymethyl)phenylamino>-5-methoxybenzoic acid 
• 89224-94-2 3-hydroxy-5-methoxy-1-phenyl-1H-indole-2-carboxylic acid methyl ester 
• 89224-76-0 6-methoxy-1-phenyl-1,2-dihydro-(4H)-3,1-benzoxazin-4-one 
• 89224-95-3 5-methoxy-2-(phenylamino)benzoic acid 

Relevant academic research and scientific papers

Enolamides, pharmaceutical compositions and methods for treating inflammation

The present invention relates to novel enolamide type compounds, pharmaceutical compositions, and methods of use thereof, useful in the treatment of diseases in which products of lipoxygenase enzyme activity or the action of leukotrienes contribute to the

Indole Esters as Heterocyclic Synthons. III . Preparation and Reactions of Furoindoles

The preparation of furoindoles via Dieckmann cyclization is described.The precursor diesters were obtained from 3-hydroxy-1H-indole-2-carboxylic acid esters and methyl or ethyl bromoacetate.Reactions of the furoindole enolic esters prepared