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It was established that photodecarbonylation of o-benzoquinones occurs by irradiation not only by UV-light, but visible light (λ>520nm) too. Study of the series of 4,5-di-substituted 3,6-di-tert-butyl-o-benzoquinones detected that the only product of photoreaction is the corresponding 3,4-di-substituted 2,5-di-tert-butyl-cyclopentadienone, which is formed in a yield close to quantitative. NMR monitoring...
Photoreduction of 9,10-phenanthrenequinone (PQ) in the presence of p-substituted N,N-dimethylanilines and polymethylbenzenes affords corresponding phenolethers as primary products. In the subsequent process shielded from light, phenolethers, which were formed by photoreaction of PQ with N,N-dimethylanilines, were quantitatively converted to give corresponding ketols. Phenolethers of 9,10-phenanthrenequinone...
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