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H<sub>3</sub>PW<sub>12</sub>O<sub>40</sub>‐Catalysed Alkylation of Arenes and Diveratrylmethanes: Convenient Routes to Triarylmethanes and to Symmetrical and Unsymmetrical 9,10‐Diaryl‐2,3,6,7‐tetramethoxyanthracenes
28
Citations
61
References
2011
Year
EngineeringOrganic ChemistryChemistryHeterocycle ChemistrySolventless ReactionsConvenient RoutesChemical EngineeringSustainable SynthesisOrganometallic CatalysisDerivativesConvenient ProtocolDiversity-oriented SynthesisCatalysisAsymmetric CatalysisEnantioselective SynthesisCatalytic SynthesisUnsymmetrical 9,10‐Diaryl‐2,3,6,7‐tetramethoxyanthracenesNatural SciencesO 40
Abstract An efficient method for the synthesis of triarylmethanes and difurylarylmethanes through solventless reactions between aldehydes and arenes in the presence of H 3 PW 12 O 40 as a reusable catalyst under thermal and microwave irradiation conditions has been developed. H 3 PW 12 O 40 ‐catalysed one‐pot consecutive Friedel–Crafts reactions between veratrole and aldehydes were also applied as a convenient protocol for the preparation of symmetrical 9,10‐diaryl‐2,3,6,7‐tetramethoxyanthracenes. The conversion of aldehydes into their corresponding acylals in the presence of H 3 PW 12 O 40 and the one‐pot reactions of diveratrylmethanes with these acylals were also used for the synthesis of symmetrical and unsymmetrical 9,10‐diaryl‐2,3,6,7‐tetramethoxyanthracenes.
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