Abstract
When catalytic quantities of superoxide ion (O.-2; or of electrons from electrolysis or of OH-) are introduced into a dry acetonitrile solution that contains excess substrate (RH), ambient air (O2), 1,2-diphenylhydrazine (PhNHNHPh), and iron(II), the substrate is rapidly and efficiently monoxygenated (e.g., triphenylphosphine----triphenylphosphine oxide, benzyl alcohol----benzaldehyde, diphenylsulfoxide----diphenylsulfone) or dehydrogenated (1,4-cyclohexadiene----benzene). The model consists of (i) an O2-activation segment that produces H2O2 from an O.-2-initiated autoxidation of disubstituted hydrazine (a model for reduced flavin), (formula; see text) and (ii) a H2O2-activation segment via the iron(II)-induced formation of ferryl ion (FeO2+), Fe(II) + H2O2----FeO2 + H2O, an effective monoxygenating agent: FeO2+ + RH----Fe(II) + ROH. The combination of i and ii provides a catalytic system for the autoxidation of organic substrates with reaction cycles that are similar to those for cytochrome P-450 monoxygenases.
Full text
PDF


Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Groves J. T., McClusky G. A. Aliphatic hydroxylation by highly purified liver microsomal cytochrome P-450. Evidence for a carbon radical intermediate. Biochem Biophys Res Commun. 1978 Mar 15;81(1):154–160. doi: 10.1016/0006-291x(78)91643-1. [DOI] [PubMed] [Google Scholar]
- Ullrich V. Cytochrome P450 and biological hydroxylation reactions. Top Curr Chem. 1979;83:67–104. doi: 10.1007/BFb0019663. [DOI] [PubMed] [Google Scholar]
- Ullrich V. Enzymatic hydroxylations with molecular oxygen. Angew Chem Int Ed Engl. 1972 Aug;11(8):701–712. doi: 10.1002/anie.197207011. [DOI] [PubMed] [Google Scholar]
- White R. E., Coon M. J. Oxygen activation by cytochrome P-450. Annu Rev Biochem. 1980;49:315–356. doi: 10.1146/annurev.bi.49.070180.001531. [DOI] [PubMed] [Google Scholar]
- White R. E., Groves J. T., McClusky G. A. Electronic and steric factors in regioselective hydroxylation catalyzed by purified cytochrome P-450. Acta Biol Med Ger. 1979;38(2-3):475–482. [PubMed] [Google Scholar]
