posted on 2020-02-12, 20:21authored byThomas
J. Paniak, Marisa C. Kozlowski
The cross-coupling
of N,N-dialkyl
aniline and aminonaphthalenes
with phenols and naphthols using a Cr–salen catalyst under
aerobic conditions was developed. Notably, air serves as an effective
oxidant affording products in high selectivity. Initial mechanistic
studies suggest an outer-sphere oxidation of the aniline/aminonaphthalene
partner, followed by nucleophilic attack of the phenol/naphthol. Single
products were observed in most cases, whereas mixtures of C–C
and C–O coupled products arose from reactions involving aminonapthalene
and sterically unencumbered phenols.