Alternative synthesis of the chiral atypical β-adrenergicphenylethanolaminotetraline agonist SR58611A using enantioselective hydrogenation
M Devocelle, A Mortreux, F Agbossou, JR Dormoy
Index: Devocelle, Marc; Mortreux, Andre; Agbossou, Francine; Dormoy, Jean-Robert Tetrahedron Letters, 1999 , vol. 40, # 24 p. 4551 - 4554
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Citation Number: 49
Abstract
We have developed an alternative synthesis of the atypical β-adrenergic phenylethanolaminotetraline agonist SR58611A. Two key intermediates have been synthesised involving enantioselective hydrogenation of an aminoketone and an enamide providing the corresponding amino alcohol and amide in> 96 and> 98% ee respectively.
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