Issue 8, 2007
From the journal:

Chemical Communications

Free-base tripyrrins†

Martin Bröring,*a   Serguei Prikhodovskia  and  Esther Cónsul Tejeroa  

* Corresponding authors

a Fachbereich Chemie, Philipps-Universität, Marburg, Germany
E-mail: Martin.Broering@chemie.uni-marburg.de
Fax: +49 6421 282 5356
Tel: +49 6421 282 5418

Abstract

The hitherto unavailable free-base tripyrrins HTrpy have been prepared by cyanide promoted demetallation of a nickel(II) tripyrrin and by acid-induced condensation of a diformylpyrrole and an alkylpyrrole with a sterically shielded α-position.

Graphical abstract: Free-base tripyrrins

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/B615935D
Article type
Communication
Submitted
02 Nov 2006
Accepted
28 Nov 2006
First published
11 Dec 2006

Chem. Commun., 2007, 876-877

Permissions

Request permissions

Free-base tripyrrins

M. Bröring, S. Prikhodovski and E. C. Tejero, Chem. Commun., 2007, 876 DOI: 10.1039/B615935D

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.

Social activity

Spotlight

Advertisements