Issue 0, 1974

The major tautomers of the pseudobases of 1,5- and 1,8-naphthyridine dications

Abstract

A recent interpretation of the structures of the pseudobases of the 1,5-dimethyl-1,5-naphthyridine and 5,6-dihydroimidazo[1,2,3-ij][1,8]naphthyridine dications which involves species bearing bridgehead hydrogen atoms is shown to be in error. The spectral data are consistent with the major pseudobase species being the expected 1,2-dihydro-2-hydroxynaphthyridines.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1974, 1833-1835

The major tautomers of the pseudobases of 1,5- and 1,8-naphthyridine dications

J. W. Bunting, J. Chem. Soc., Perkin Trans. 1, 1974, 1833 DOI: 10.1039/P19740001833

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