Issue 1, 2006
From the journal:

Organic & Biomolecular Chemistry

Aromatic annulation strategy for naphthalenes fused at 1,2- and 3,4-positions with two heterocycles†

Min Zhang,a   Hui-Ying An,a   Bao-Guo Zhaoa  and  Jian-Hua Xu*a  

* Corresponding authors

a Department of Chemistry, Nanjing University, Nanjing, P. R. China
E-mail: xujh@nju.edu.cn
Fax: (+86)25 8331 7761
Tel: (+86)25 8359 2709

Abstract

An efficient regioselective naphthoannulation strategy able to fuse a newly formed naphthalene ring at its 1,2- and 3,4- positions to two different heterocycles has been developed.

Graphical abstract: Aromatic annulation strategy for naphthalenes fused at 1,2- and 3,4-positions with two heterocycles

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Article information

DOI
https://doi.org/10.1039/B514496E
Article type
Communication
Submitted
14 Oct 2005
Accepted
01 Nov 2005
First published
18 Nov 2005

Org. Biomol. Chem., 2006,4, 33-35

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Aromatic annulation strategy for naphthalenes fused at 1,2- and 3,4-positions with two heterocycles

M. Zhang, H. An, B. Zhao and J. Xu, Org. Biomol. Chem., 2006, 4, 33 DOI: 10.1039/B514496E

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