Publication | Closed Access
Metal‐Free Direct Aryltrifluoromethylation of Allylic Alcohols with Langlois’ Reagent through Concomitant 1,2‐Aryl Migration
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Citations
57
References
2015
Year
Concomitant 1,2‐ArylCross-coupling ReactionEngineeringNatural SciencesDiversity-oriented SynthesisAllylic AlcoholsOrganic ChemistryMetal‐free Direct AryltrifluoromethylationOrganometallic CatalysisChemistryCf 3Synthetic ChemistryBiomolecular EngineeringCost‐effective Synthetic Protocol
Abstract A metal‐free and cost‐effective synthetic protocol for selective aryltrifluoromethylation of allylic alcohols with Langlois’ reagent (CF 3 SO 2 Na) through cascade trifluoromethyl radical addition/1,2‐aryl migration has been developed. The highlights of this procedure are operational simplicity, excellent functional group tolerance, and mild reaction conditions.
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