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Air-Stable Trialkylphosphonium Salts:  Simple, Practical, and Versatile Replacements for Air-Sensitive Trialkylphosphines. Applications in Stoichiometric and Catalytic Processes

Organic Letters · 2001 · Vol. 3(26) · pp. 4295–4298
Matthew R. NethertonGregory C. Fu

Abstract

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]

Synthetic Organic Chemistry MethodsAsymmetric Synthesis and CatalysisChemical Synthesis and ReactionsChemistryPhosphoniumDeprotonationProtonationReactivity (psychology)CatalysisCombinatorial chemistryStoichiometrySimple (philosophy)Base (topology)

MeSH terms

AirCatalysisOxidation-ReductionPhosphines

Funding

  • Pfizer
Citations
596
FWCI
22.86
field-weighted impact
References
8
Percentile
100%
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Citations per year
References
Selective reduction of disulfides by tris(2-carboxyethyl)phosphine
The Journal of Organic Chemistry · 1991 · 685 citations
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