Issue 2, 1988

Thermolysis of polyazapentadienes. Part 9. Gas phase thermolyses of some dienamines, enaminones, and enaminothiones

Abstract

Thermolysis of the title compounds gives low yields of pyrroles by a hydrogen-transfer–cyclisation–aromatisation sequence. The results are best explained by a dipolar mechanism for the hydrogen-transfer step: competitive aromatisation routes account for the range of substituted pyrroles which were obtained.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1988, 339-342

Thermolysis of polyazapentadienes. Part 9. Gas phase thermolyses of some dienamines, enaminones, and enaminothiones

C. L. Hickson and H. McNab, J. Chem. Soc., Perkin Trans. 1, 1988, 339 DOI: 10.1039/P19880000339

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