Azaanthraquinoneassembly from N-propargylamino quinoneviaiodine-induced 6-endo-dig electrophilic cyclization†
Abstract
An efficient methodology taking advantage of the excellent nucleophilicity of
* Corresponding authors
a
School of Chemistry and Chemical Engineering, State Key Laboratory of Coordination Chemistry, Nanjing University, Nanjing 210093, P. R. China
E-mail:
wangsz@nju.edu.cn
Fax: +86 25 83317761
Tel: +86 25 83593732
b Modern Analytical Center of Nanjing University, Nanjing 210093, P. R. China
An efficient methodology taking advantage of the excellent nucleophilicity of
N. Fei, Q. Hou, S. Wang, H. Wang and Z. Yao, Org. Biomol. Chem., 2010, 8, 4096 DOI: 10.1039/C004896H
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.
Fetching data from CrossRef.
This may take some time to load.
Loading related content