3-Hydroxypyrroles and 1H-pyrrol-3(2H)-ones. Part 4. Oxidation of 2-monosubstituted and 2-unsubstituted pyrrolones, with an electron spin resonance study of a dimeric intermediate
作者:Hamish McNab、Lilian C. Monahan、John C. Walton
DOI:10.1039/p29880000759
日期:——
Oxidation of 2-substituted 1H-pyrrol-3(2H)-ones in air gives 2-hydroxy derivatives, which can exist in solvent-dependent equilibrium with open-chain acyl enaminones. Oxidation of 2-unsubstitued analogues by irradiation in the presence of di-t-butyl peroxide gives rise to persistent radicals, identified as pyrrolone dimers [e.g.(21)] by e.s.r. spectroscopy. The formation of the various products is rationalised
Thermal functionalisation of nitrogen substituents: formation of dihydropyrrol-3-ones, quinolin-4-ones, and enaminoenaminones by gas-phase hydrogen transfer reactions
作者:Helen J. Gordon、Jane C. Martin、Hamish McNab
DOI:10.1039/c39830000957
日期:——
(5-aminomethylene-2,2-dimethyl-1,3-dioxane-4,6-dione)(1), (7), (11), and (12) causes hydrogentransferreactions which result in specific functionalisation of the amino substituent: tertiary amino substrates give 1,2-dihydropyrrol-3-ones (60%) by ring closure, while secondary amino substrates give quinolin-4-ones (90%) or enaminoenaminones (90%).