Issue 0, 1966

Cyclitols. Part XXIII. Suppression of epoxide migration. Synthesis of mucoinositol

Abstract

A strong-base ion-exchange resin converts 1-O-toluene-p-sulphonylmyoinositol into 1,2-anhydro-(±)-inositol but, unlike sodium hydroxide, does not cause subsequent epoxide migration. Acid hydrolysis of the anhydro-compound gives mainly mucoinositol. The configurations of “bromoscylloquercitol” and “bromoviboquercitol” have been established.

Article information

Article type
Paper

J. Chem. Soc. C, 1966, 798-800

Cyclitols. Part XXIII. Suppression of epoxide migration. Synthesis of mucoinositol

S. J. Angyal, V. Bender and J. H. Curtin, J. Chem. Soc. C, 1966, 798 DOI: 10.1039/J39660000798

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