Journal of Medicinal Chemistry p. 149 - 153 (1981)
Update date:2022-08-03
Topics: Synthesis Assessment
Cannon, Joseph G.
Brubaker, Abram N.
Long, John Paul
Flynn, Jan R.
Verimer, Turkiz
et al.
Replacement of the catechol 3,4-dihydroxylation pattern of certain adrenergic β-phenethylamines by a resorcinol 3,5-dihydroxylation pattern has led to greater selectivity of adrenergic agonist effects in certain molecules.This strategy has been applied to
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(2018)Doi:10.1016/0009-3084(95)02475-X
(1995)Doi:10.1002/anie.201912753
(2020)Doi:10.1016/j.bmc.2004.04.037
(2004)Doi:10.1246/bcsj.54.3522
(1981)
