Issue 17, 1976

Photosensitised oxidation of 1-naphthols

Abstract

Whereas oxidation of 1-naphthols with Fremy's salt often affords significant amounts of the corresponding 1,2-naphthoquinone dye-sensitised photo-oxidation gives exclusively the 1,4-naphthoquinone via the addition of singlet oxygen to the naphthalene ring.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1976, 676-677

Photosensitised oxidation of 1-naphthols

J. Griffiths, K. Chu and C. Hawkins, J. Chem. Soc., Chem. Commun., 1976, 676 DOI: 10.1039/C39760000676

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