Publication | Open Access
Stereoselective reduction of 1-acyl-2-phenylacetylenes with triphenylphosphine in water: efficient synthesis of E-chalcones
12
Citations
1
References
2011
Year
High YieldsRoom TemperatureChemical EngineeringOrganic SolventEngineeringAlkene MetathesisDerivative (Chemistry)Organic ChemistryCatalysisEfficient SynthesisChemistryStereoselective SynthesisStereoselective ReductionAsymmetric CatalysisChemical DerivativeSynthetic ChemistryEnantioselective Synthesis
1-Acyl-2-phenylacetylenes are reduced with triphenylphosphine in water under mild conditions (room temperature, without catalyst and organic solvent, 3 h) to afford (E)-1-acyl-2phenylethenes (chalcones) in high yields (83-91%).
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