Issue 44, 2012
From the journal:

Organic & Biomolecular Chemistry

An efficient synthesis of heptaaryldipyrromethenes from tetraarylcyclopentadienones and ammonium acetate and their extension to the corresponding BODIPYs†

Jichao Li,a   Binbin Hu,a   Gongfang Hu,a   Xihui Li,a   Ping Lu*a  and  Yanguang Wang*a  

* Corresponding authors

a Department of Chemistry, Zhejiang University, Hangzhou 310027, P. R. China
E-mail: pinglu@zju.edu.cn
Fax: (+86) 571-87952543

Abstract

Heptaaryldipyrromethenes are efficiently prepared from ammonium acetate and tetraarylcyclopentadienones in a one-pot cascade process and can be converted into heptaaryl BODIPYs with fluorescent response to environmental acidity.

Graphical abstract: An efficient synthesis of heptaaryldipyrromethenes from tetraarylcyclopentadienones and ammonium acetate and their extension to the corresponding BODIPYs

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Article information

DOI
https://doi.org/10.1039/C2OB26509E
Article type
Paper
Submitted
01 Aug 2012
Accepted
17 Sep 2012
First published
18 Sep 2012

Org. Biomol. Chem., 2012,10, 8848-8859

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An efficient synthesis of heptaaryldipyrromethenes from tetraarylcyclopentadienones and ammonium acetate and their extension to the corresponding BODIPYs

J. Li, B. Hu, G. Hu, X. Li, P. Lu and Y. Wang, Org. Biomol. Chem., 2012, 10, 8848 DOI: 10.1039/C2OB26509E

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