Issue 5, 1972

The chemistry of reactive lignin intermediates. Part I. Transients in coniferyl alcohol photolysis

Abstract

Photolysis of coniferyl alcohol produces a transient quinone methide. The rates of decay of this quinone methide have been measured in water, acetic acid, and propane-1,2-diol. The possible significance of the quinone methide in lignin biosynthesis is discussed.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 2, 1972, 640-642

The chemistry of reactive lignin intermediates. Part I. Transients in coniferyl alcohol photolysis

G. Leary, J. Chem. Soc., Perkin Trans. 2, 1972, 640 DOI: 10.1039/P29720000640

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