Publication | Closed Access
Allyl‐Palladium‐Catalyzed α,β‐Dehydrogenation of Carboxylic Acids via Enediolates
46
Citations
29
References
2017
Year
Allyl‐palladium CatalysisCross-coupling ReactionEngineeringStep‐economic αOrganic ChemistryCatalysisExcess Zncl 2ChemistryAllyl‐palladium‐catalyzed αAsymmetric CatalysisEnantioselective SynthesisBiomolecular Engineering
Abstract A highly practical and step‐economic α,β‐dehydrogenation of carboxylic acids via enediolates is reported through the use of allyl‐palladium catalysis. Dianions underwent smooth dehydrogenation when generated using Zn(TMP) 2 ⋅2 LiCl as a base in the presence of excess ZnCl 2 , thus avoiding the typical decarboxylation pathway of these substrates. Direct access to 2‐enoic acids allows derivatization by numerous approaches.
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