85278-54-2

Upstream product

• 85278-85-9 (E)-1-fluoro-2-(3,4-dihydroxyphenyl)-3-phthalimidoprapene 
• 13790-42-6 tert-butyl 3,4-dimethoxyphenylacetate 
• 85277-77-6 (E)-ethyl 2-(3,4-dimethoxyphenyl)-3-fluoroacrylate 
• 85277-60-7 ethyl 2-(tert-butoxycarbonyl)-2-(3,4-dimethoxyphenyl)acetate 
• 85277-95-8 (E)-1-fluoro-2-(3,4-dimethoxyphenyl)-3-phthalimidopropene 
• 85277-70-9 ethyl 2-(tert-butoxycarbonyl)-2-(difluoromethyl)-2-(3,4-dimethoxyphenyl)acetate 
• 85277-86-7 (E)-2-(3,4-dimethoxyphenyl)-3-fluoroprop-2-en-1-ol 

Relevant academic research and scientific papers

Enzyme-activated irreversible inhibitors of monoamine oxidase: Phenylallylamine structure-activity relationships

Seventeen 2-aryl-3-haloallylamine derivatives were prepared and evaluated as inhibitors of monoamine oxidase (MAO, EC 1.4.3.4). The synthesis of these compounds was achieved from either α-methylstyrene or ring-substituted phenylacetic acid derivatives. Wi