Publication | Closed Access
Dual Catalysis: Proton/Metal-Catalyzed Tandem Benzofuran Annulation/Carbene Transfer Reaction
92
Citations
38
References
2016
Year
O-quinone MethideChemical EngineeringDft-based Computational StudiesDerivativesEngineeringHeterocyclicCross-coupling ReactionNatural SciencesDiversity-oriented SynthesisBenzofuryl CarbeneOrganic ChemistryDual CatalysisOrganometallic CatalysisCatalysisMolecular CatalysisChemistryBiomolecular Engineering
An efficient proton/metal-catalyzed tandem benzofuran annulation/carbene transfer reaction for the synthesis of various benzofuryl-substituted cyclopropanes and cycloheptatrienes has been developed. The reaction was proposed to proceed through two key intermediates, o-quinone methide (o-QM) and benzofuryl carbene. The DFT-based computational studies indicated that the reaction was initiated through the dehydration of o-HBA via a Brønsted acid mediated proton shuttle transition state, forming the key intermediate o-QM.
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