Journal of Medicinal Chemistry p. 186 - 193 (1985)
Update date:2022-07-29
Topics:
McDonald
Lacoste
Bey
Palfreyman
Zreika
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
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Doi:10.1039/jr9380000672
(1938)Doi:10.1016/0040-4020(82)80187-7
(1982)Doi:10.1021/ja01239a015
(1944)Doi:10.1021/ja01846a073
(1941)Doi:10.1039/c2gc36652e
(2013)Doi:10.1021/ja01650a032
(1954)
