Abstract
Tricarbonyliron complexes of α-substituted dienones are well suited starting compounds for the synthesis of diastereomerically pure 1,2,3-trisubstituted 1,3-diols of known configuration, among them 1,2,3-triols. This is achieved by aldol condensation with an aldehyde, a reaction which gives one distinctly major isolated ketol, under Mukayiama conditions, followed by totally stereoselective reduction.
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