Issue 0, 1972

Carcinogenic nitrogen compounds. Part LXXIX. A route to new condensed acridines containing a cyclopent[kl]acridine nucleus

Abstract

The reaction of 7-o-chlorophenylbenz[c]acridine with sodium hydroxide in benzo[h]quinoline affords a mixture of 7-phenylbenz[c]acridine, benz[c]indeno[1,3-kl]acridine, and benz[c]indeno[1,3-mn]acridine; a similar cyclisation of 7-o-chlorophenyldibenz[c,h]acridine leads to dibenz[c,h]indeno[1,3-kl]acridine, whereas the isomeric 14-o-chlorophenyldibenz[a,h]acridine gives a mixture of dibenz[a,h]acridine and benzo[h]phenanthro-[9,10,1-mna]acridine.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1972, 1263-1266

Carcinogenic nitrogen compounds. Part LXXIX. A route to new condensed acridines containing a cyclopent[kl]acridine nucleus

N. P. Buu-Hoï, O. Périn-Roussel, P. Jacquignon and A. Cheutin, J. Chem. Soc., Perkin Trans. 1, 1972, 1263 DOI: 10.1039/P19720001263

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