articleTop 1% cited
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. Netherton✉(Massachusetts Institute of Technology)Gregory C. Fu(Massachusetts Institute of Technology)
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%
vs. same field & year
Citations per year
Cited by
Establishment of Broadly Applicable Reaction Conditions for the Palladium-Catalyzed Direct Arylation of Heteroatom-Containing Aromatic Compounds
The Journal of Organic Chemistry · 2009 · 590 citations
Recent applications of the Suzuki–Miyaura cross-coupling reaction in organic synthesis
Tetrahedron · 2002 · 1,680 citations
Controlled Microwave Heating in Modern Organic Synthesis
Angewandte Chemie International Edition · 2004 · 3,526 citations
References
Selective reduction of disulfides by tris(2-carboxyethyl)phosphine
The Journal of Organic Chemistry · 1991 · 685 citations
Citation Network
How this paper connects to the literature. Drag to explore, click any node to open that paper.
