Issue 0, 1968

Periodate oxidation of 4,4,6,6-tetramethylcyclohexane-1,2,3-triol

Abstract

The periodate oxidation of 4,4,6,6-tetramethylcyclohexane-1,2,3-triol in neutral or acidic aqueous solution did not give the expected 2,2,4,4-tetramethylpentane-1,5-dial, but exo-7-hydroxy-2,2,4,4-tetramethyl-6,8-dioxabicyclo[3,2,1]octane, produced by a partial oxidation to the hydroxy-dialdehyde, followed by closure of two intramolecular acetal linkages to give the observed product.

Article information

Article type
Paper

J. Chem. Soc. C, 1968, 7-8

Periodate oxidation of 4,4,6,6-tetramethylcyclohexane-1,2,3-triol

J. S. McConaghy and J. J. Bloomfield, J. Chem. Soc. C, 1968, 7 DOI: 10.1039/J39680000007

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