| Literature DB >> 32049541 |
Thomas J Paniak1, Marisa C Kozlowski1.
Abstract
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.Entities:
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Year: 2020 PMID: 32049541 PMCID: PMC7060808 DOI: 10.1021/acs.orglett.0c00046
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005