Issue 11, 2001
From the journal:

Chemical Communications

A one-step synthesis of a free base secochlorin from a 2,3-dimethoxy porphyrinElectronic supplementary information (ESI) available: experimental details. See http://www.rsc.org/suppdata/cc/b1/b102139g/

Jonathan L. Sessler,*a   Sergiy V. Shevchuk,a   Wyeth Callawaya  and  Vincent Lyncha  

* Corresponding authors

a Department of Chemistry and Biochemistry, Institute for Cellular and Molecular Biology, The University of Texas at Austin, Austin, USA.
E-mail: sessler@mail.utexas.edu;
Fax: 1-512-471-7550

Abstract

The synthesis and X-ray structure of a C2 symmetric secochlorin 2, obtained by a photosensitized oxidative ring opening of a 2,3-dimethoxy porphyrin, is described.

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Article information

DOI
https://doi.org/10.1039/B102139G
Article type
Communication
Submitted
07 Mar 2001
Accepted
05 Apr 2001
First published
10 May 2001

Chem. Commun., 2001, 968-969

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A one-step synthesis of a free base secochlorin from a 2,3-dimethoxy porphyrin

J. L. Sessler, S. V. Shevchuk, W. Callaway and V. Lynch, Chem. Commun., 2001, 968 DOI: 10.1039/B102139G

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