Issue 7, 1994

Ozone-mediated nitration of aromatic ketones and related compounds with nitrogen dioxide

Abstract

Alkyl aryl ketones react smoothly with nitrogen dioxide at low temperatures in the presence of ozone to give ortho- and meta-nitro derivatives as the principal products, the former usually being predominant (ortho : meta= 1.1–3.8 : 1.0). No attack was observed on the alkyl side chains.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1994, 903-908

Ozone-mediated nitration of aromatic ketones and related compounds with nitrogen dioxide

H. Suzuki and T. Murashima, J. Chem. Soc., Perkin Trans. 1, 1994, 903 DOI: 10.1039/P19940000903

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