| Literature DB >> 20838686 |
Robert Lechner1, Susanne Kümmel, Burkhard König.
Abstract
We report the photocatalytic oxidation of benzylic carbon atoms under mild conditions using riboflavin tetraacetate as photocatalyst and blue-emitting LEDs (440 nm) as light source. Oxygen is the terminal oxidant and hydrogen peroxide appears as the only byproduct in most cases. The process oxidizes toluene derivatives, stilbenes, styrenes and phenylacetic acids to their corresponding benzaldehydes. A benzyl methyl ether and acylated benzyl amines are oxidized directly to the corresponding methyl ester or benzylimides. The mechanism of the reactions has been investigated and the results indicate that oxygen addition to benzyl radicals is a key step of the oxidation process in the case of phenylacetic acids.Entities:
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Year: 2010 PMID: 20838686 DOI: 10.1039/c0pp00202j
Source DB: PubMed Journal: Photochem Photobiol Sci ISSN: 1474-905X Impact factor: 3.982