Publication | Closed Access
Unprecedented Synthesis of Alkynylphosphine-boranes through Room-Temperature Oxidative Alkynylation
42
Citations
24
References
2013
Year
Cross-coupling ReactionEngineeringUnprecedented SynthesisSecondary PhosphineOrganic ChemistryOrganometallic CatalysisCatalysisChemistryUser-friendly SynthesisHeterocycle ChemistryAvailable Copper AcetylidesAsymmetric CatalysisSynthetic ChemistryEnantioselective SynthesisBiomolecular Engineering
An original and user-friendly synthesis of alkynylphosphine-boranes, useful building blocks in organic synthesis, based on an oxidative P-alkynylation reaction with readily available copper acetylides is reported. The ability of a secondary phosphine protected with a borane to undergo oxidative coupling without oxidation of the P-moiety is demonstrated for the first time. The reaction, which proceeds at room temperature, is applicable to the preparation of enantioenriched and structurally complex alkynylphosphine-boranes.
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