Organic Letters · 2001 · 598 citations · 6 references
Natural SciencesChemical EngineeringChemistryCatalysisInorganic ChemistryOrganometallic ChemistryCatalytic MechanismsOrganometallic ReactivityMild Reaction ConditionsPhosphine ReactivityStability Under Reaction Conditions
Trialkylphosphines furnish unusual, sometimes unique, reactivity in a range of transformations. Unfortunately, their utility is compromised by their sensitivity to oxidation. We have examined a simple but powerful strategy for addressing this problem: convert air-sensitive trialkylphosphines into air-stable phosphonium salts via protonation on phosphorus. These robust salts serve as direct replacements for the corresponding phosphines (simple deprotonation under the reaction conditions by a Brønsted base liberates the trialkylphosphine) in a diverse set of applications. [reaction: see text]
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Selective reduction of disulfides by tris(2-carboxyethyl)phosphine
John A. Burns, James C. Butler, John T. Moran et al. · The Journal of Organic Chemistry · 1991 · 689 citations
Lars R. Furenlid, Mark W. Renner, David J. Szalda et al. · Journal of the American Chemical Society · 1991 · 96 citations
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