Abstract
A direct catalytic asymmetric aldol reaction of aromatic aldehydes and thioamides is described. A soft Lewis acid/hard Brønsted base cooperative catalyst comprising ( R, R)-Ph-BPE/[Cu(CH 3CN) 4]PF 6/Li(OC 6H 4- p-OMe) promoted the title reaction efficiently, triggered by in situ generation of the active thioamide enolate through a soft–soft interaction of Cu(I) and the thioamide. The aldol product was transformed into ( R)-fluoxetine, an antidepressant agent.
Published Version
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