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Palladium‐Catalyzed Enantioselective Domino Reaction for the Efficient Synthesis of Vitamin E
160
Citations
38
References
2004
Year
Vitamin EMedicinal ChemistryCross-coupling ReactionEngineeringNatural SciencesOrganic ChemistryChiral Chroman 2CatalysisEfficient SynthesisChemistryStereoselective SynthesisNatural Product SynthesisAsymmetric CatalysisEnantioselective SynthesisBiomolecular EngineeringNew Route
A new route to vitamin E: The palladium-catalyzed enantioselective domino reaction of the unsaturated phenol derivative 1 with acrylate provides efficient access to the chiral chroman 2 with 96 % ee and in 84 % yield (see scheme). Intermediate 2 can then be converted into vitamin E in a few steps.
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