Issue 0, 1980

Oxidative coupling of phenols and phenolic ethers. Part 4. Synthesis of dibenz[d,f]azonines and a dibenz[d,f]azacine, via direct coupling

Abstract

Two series of amides, the N-phenethylphenylacetamides (9) and the bisphenethylamides (11), including diphenolic monophenolic, and non-phenolic types, were treated with a range of one-electron oxidants. With the tetramethoxy-derivative (11e) intramolecular coupling yielded a dibenzazonine (16) in 36% yield. Similar oxidation of the homologue (18) gave a dibenzazecine (19) in 60% yield.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1980, 1104-1108

Oxidative coupling of phenols and phenolic ethers. Part 4. Synthesis of dibenz[d,f]azonines and a dibenz[d,f]azacine, via direct coupling

E. McDonald and R. D. Wylie, J. Chem. Soc., Perkin Trans. 1, 1980, 1104 DOI: 10.1039/P19800001104

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