Issue 18, 2003
From the journal:

Chemical Communications

Benzoylbiliverdins from chemical oxidation of dodeca-substituted porphyrins†

Owendi Ongayi,a   Frank R. Fronczeka  and  M. Graça H. Vicente*a  

* Corresponding authors

a Department of Chemistry, Louisiana State University, Baton Rouge, LA 70803, USA

Abstract

Oxidation of dodeca-substituted porphyrin 1 in the presence of NaNO2/TFA and air afforded benzoylbiliverdin 3 in 77% yield; under similar conditions the Ni(II)-porphyrin 2 was mainly nitrated at a cyclohexenyl ring; key X-ray structures are presented.

Graphical abstract: Benzoylbiliverdins from chemical oxidation of dodeca-substituted porphyrins

About
Cited by
Related
Download options Please wait...

Supplementary files

Additions and corrections

Article information

DOI
https://doi.org/10.1039/B306586C
Article type
Communication
Submitted
09 Jun 2003
Accepted
17 Jul 2003
First published
04 Aug 2003

Chem. Commun., 2003, 2298-2299

Permissions

Request permissions

Benzoylbiliverdins from chemical oxidation of dodeca-substituted porphyrins

O. Ongayi, F. R. Fronczek and M. G. H. Vicente, Chem. Commun., 2003, 2298 DOI: 10.1039/B306586C

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