Enantioselective organocatalytic aryloxylation of aldehydes with o-quinones

An enantioselective organocatalytic inverse electron demand hetero Diels-Alder reaction of in situ generated enamines with o-quinone reagents is reported. The method, which is optimal in wet acetonitrile at ambient temperature, provides a new and direct asymmetric route to the aryl alkyl ether motif and an alternative metal-free strategy to SN2 substitutions with phenolate nucleophiles.

An enantioselective organocatalytic inverse electron demand hetero Diels-Alder reaction of in situ generated enamines of aldehydes with ortho-quinone reagents is reported.