Issue 0, 1968

Assignment of configurations to the 1,3,4,7-tetramethylisoindolines by use of nuclear magnetic resonance spectroscopy

Abstract

The configurations of the 1,3,4,7-tetramethylisoindolines have been assigned on the basis of the equivalence or otherwise of the methylene protons in the N-benzyl and N-neopentyl derivatives. The isomer of lower m.p. has the cis-configuration. The acid-catalysed thermal equilibration of the isomers has been demonstrated.

Article information

Article type
Paper

J. Chem. Soc. C, 1968, 2186-2188

Assignment of configurations to the 1,3,4,7-tetramethylisoindolines by use of nuclear magnetic resonance spectroscopy

C. O. Bender and R. Bonnett, J. Chem. Soc. C, 1968, 2186 DOI: 10.1039/J39680002186

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