Issue 6, 2009

New domino reaction for the selective synthesis of tetracyclic cinnolino[5,4,3-cde]cinnolines

Abstract

A new domino reaction for the highly selective synthesis of tetracyclic cinnolino[5,4,3-cde]cinnolines using steric control was described. In this reaction, the use of anthenes with aliphatic groups (R1) leads to cinnolino[5,4,3-cde]cinnolines whereas anthenes with aryl groups (R1) result in N-amino-1,8-dioxoacridines.

Graphical abstract: New domino reaction for the selective synthesis of tetracyclic cinnolino[5,4,3-cde]cinnolines

Supplementary files

Article information

Article type
Paper
Submitted
13 Oct 2008
Accepted
15 Dec 2008
First published
29 Jan 2009

Org. Biomol. Chem., 2009,7, 1171-1175

New domino reaction for the selective synthesis of tetracyclic cinnolino[5,4,3-cde]cinnolines

B. Jiang, W. Hao, J. Zhang, S. Tu and F. Shi, Org. Biomol. Chem., 2009, 7, 1171 DOI: 10.1039/B817930A

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