Issue 24, 1996

A new ring system: 3-H-pyrazolo[3,4-h]isoquinoline. An unexpected product from diazotization of an aminoisoquinoline

Abstract

Diazotization of 7-amino-5,8-dimethyl-6-thiophenylisoquinoline with sodium nitrite in acetic acid gives a mixture of 6-thiaellipticine and 5-methyl-4-thiophenyl-3H-pyrazolo[3,4-h]isoquinoline, a new heterocyclic ring system whose crystal structure is presented.

Article information

Article type
Paper

Chem. Commun., 1996, 2711-2712

A new ring system: 3-H-pyrazolo[3,4-h]isoquinoline. An unexpected product from diazotization of an aminoisoquinoline

R. B. Miller, J. G. Stowell, C. W. Jenks, S. C. Farmer, C. E. Wujcik and M. M. Olmstead, Chem. Commun., 1996, 2711 DOI: 10.1039/CC9960002711

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.

Social activity

Spotlight

Advertisements