Issue 7, 2001

Novel bis(tetrahydropyrrolo[3,4-b]carbazoles) linked with aliphatic chains: synthesis and structural aspects

Abstract

Syntheses of novel bis(tetrahydropyrrolo[3,4-b]carbazoles) by a [4+2]cycloaddition reaction are described. By variation of dienophiles bis(tetrahydropyrrolo[3,4-b]carbazoles) of varying aliphatic spacer length could be obtained in high yields. These conformationally highly flexible molecules represent an interesting class of compounds, believed to have an affinity towards DNA, as potential DNA ligands.

Graphical abstract: Novel bis(tetrahydropyrrolo[3,4-b]carbazoles) linked with aliphatic chains: synthesis and structural aspects

Article information

Article type
Paper
Submitted
05 Dec 2000
Accepted
19 Feb 2001
First published
20 Mar 2001

J. Chem. Soc., Perkin Trans. 1, 2001, 695-700

Novel bis(tetrahydropyrrolo[3,4-b]carbazoles) linked with aliphatic chains: synthesis and structural aspects

K. U. Meyer and U. Pindur, J. Chem. Soc., Perkin Trans. 1, 2001, 695 DOI: 10.1039/B009731O

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