Issue 16, 1981

Thermal racemization of a chiral arene oxide metabolite: chrysene 3,4-oxide

Abstract

Chrysene 3,4-oxide, a major initial mammalian metabolite of chrysene, now synthesised in optically active form and configurationally assigned, has been found to racemize thermally with an activation energy of 25·2 kcal mol–1, consistent with an earlier perturbational molecular orbital calculation-predicted oxepin intermediate mechanism.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1981, 838-839

Thermal racemization of a chiral arene oxide metabolite: chrysene 3,4-oxide

D. R. Boyd, M. G. Burnett and R. M. E. Greene, J. Chem. Soc., Chem. Commun., 1981, 838 DOI: 10.1039/C39810000838

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements