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Issue 11, 2001
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A one-step synthesis of a free base secochlorin from a 2,3-dimethoxy porphyrin

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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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Publication details

The article was received on 07 Mar 2001, accepted on 05 Apr 2001 and first published on 10 May 2001


Article type: Communication
DOI: 10.1039/B102139G
Citation: Chem. Commun., 2001,0, 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, 0, 968
    DOI: 10.1039/B102139G

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