The synthesis of a series of 1-(aryloxy)-3-[[(amido)alkyl]amino]propan-2-ols where either the aryl moiety is heterocyclic or the amidic group is substituted by a heterocyclic moiety is described. Several of the compounds were more potent that propranolol
Large,Smith
p. 1417 - 1422
(2007/10/02)
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