Issue 16, 1998

Synthesis of aminoquinolones from triazoles via carboxamidoketenimine and amidinoketene intermediates

Abstract

1-Aryl-1H-1,2,3-triazole-4-carboxamides 7d–f have been synthesized and converted to 2-dimethylamino-4-quinolones 12d–f by flash vacuum thermolysis (FVT). The reaction takes place via carboxamidoketenimine 9 and amidinoketene intermediates 10. The former are observed by FTIR spectroscopy at 77 K or in Ar matrices at 12 K.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1998, 2583-2586

Synthesis of aminoquinolones from triazoles via carboxamidoketenimine and amidinoketene intermediates

V. V. Ramana Rao and C. Wentrup, J. Chem. Soc., Perkin Trans. 1, 1998, 2583 DOI: 10.1039/A802768D

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