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Updated: Apr 21, 2026

Facile Preparation of 2Z,4E-Dienamides by the Olefination of Electron-deficient Alkenes with Allyl Acetate
Published on: June 21, 2017
Ruthenium-catalyzed tandem-isomerization/asymmetric transfer hydrogenation of allylic alcohols
Tove Slagbrand1, Helena Lundberg, Hans Adolfsson
1Dept. of Organic Chemistry, Stockholm University, The Arrhenius Laboratory, 10691 Stockholm (Sweden).
Abstract:
A one-pot procedure for the direct conversion of racemic allylic alcohols to enantiomerically enriched saturated alcohols is presented. The tandem-isomerization/asymmetric transfer hydrogenation process is efficiently catalyzed by [{Ru(p-cymene)Cl2 }2 ] in combination with the α-amino acid hydroxyamide ligand 1, and performed under mild conditions in a mixture of ethanol and THF. The saturated alcohol products are isolated in good to excellent chemical yields and in enantiomeric excess up to 93 %.
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