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1 Department of Pharmacology, West Virginia University School of Medicine, Morgantown, W. Va.
The replacement of the hydrogen atom in the para position of phenethylamine and phenethyl-methylamine with a fluorine atom leads to compounds that are more active as sympathomimetic amines, although not as active as tyramine, the compound with a hydroxy group in the para position of the phenethylamine molecule.
Submitted on July 12, 1948