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Regioselective Reductive Coupling of Alkynes and Aldehydes Leading to Allylic Alcohols
84
Citations
16
References
2003
Year
Terminal AlkyneCross-coupling ReactionEngineeringCatalytic AmountAlkene Metathesis1,2-Disubstituted Allylic AlcoholAllylic AlcoholsOrganic ChemistryCatalysisChemistryRegioselective Reductive CouplingAsymmetric CatalysisEnantioselective SynthesisAldehydes Leading
Treatment of a mixture of a terminal alkyne and an aldehyde with CrCl(2) and a catalytic amount of NiCl(2) and triphenylphosphine in the presence of water in DMF at 25 degrees C gives a 1,2-disubstituted allylic alcohol regioselectively.
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