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FLUORIDE-INDUCED 1,2-ELIMINATION OF <i>O</i>-TRIMETHYLSILYLPHENYL TRIFLATE TO BENZYNE UNDER MILD CONDITIONS
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Citations
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References
1983
Year
HalogenationAbstract Fluoride-induced 1,2-EliminationO-trimethylsilylphenyl TriflateMild ConditionsFluorous SynthesisOrganic ChemistryChemistryPharmacologyFluoride-induced 1,2-Elimination
Abstract Fluoride-induced 1,2-elimination of o-trimethylsilylphenyl triflate provided a convenient route to benzyne under mild conditions where detriflation from an intermediary aryl anion appeared to occur in preference to protonation even in the presence of alcohols.
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