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Selective Rhodium-Catalyzed Hydroformylation of Alkynes to α,β-Unsaturated Aldehydes with a Tetraphosphoramidite Ligand
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Citations
25
References
2016
Year
Asymmetric CatalysisCross-coupling ReactionEngineeringSelective Rhodium-catalyzed HydroformylationNatural SciencesDiversity-oriented SynthesisIndenamine Derivativesβ-Unsaturated AldehydesTetraphosphoramidite LigandOrganic ChemistryOrganometallic CatalysisCatalysisChemistryRh-catalyzed HydroformylationEnantioselective SynthesisBiomolecular Engineering
A tetraphosphoramidite ligand was successfully applied to a Rh-catalyzed hydroformylation of various symmetrical and unsymmetrical alkynes to afford corresponding α,β-unsaturated aldehyde products in good to excellent yields (up to 97% yield). Excellent chemo- and regioselectivities and high activities (up to 20 000 TON) were achieved. The corresponding α,β-unsaturated aldehyde products can be transformed into many useful and important organic molecules, such as indenamine derivatives and lukianol pyrroles. This great performance makes the hydroformylation of alkynes highly practical with great potential.
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