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Solvent-free preparation of amidoalkyl phenols catalyzed by trityl chloride under neutral media
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Citations
19
References
2015
Year
Chemical EngineeringCross-coupling ReactionInherent InstabilityEngineeringEnantioselective SynthesisNovel OrganocatalystsSolvent-free PreparationOrganic ChemistryCatalysisMolecular CatalysisChemistryHomogeneous OrganocatalystAsymmetric CatalysisSynthetic ChemistryNeutral MediaCatalytic SynthesisAmidoalkyl Phenols
A one-pot, multicomponent condensation reaction of phenols, aromatic aldehydes, and amides in the presence of catalytic amount of trityl chloride as a homogeneous organocatalyst under solvent-free condition to prepare amidoalkyl phenols has been reported. It is interesting that trityl chloride by in situ generation of trityl carbocation with inherent instability catalyzes the reaction.
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