Issue 20, 1999
From the journal:

Chemical Communications

Reduction of N-arylporphyrins to N-arylphlorins: opposite stereochemical courses as a function of the reducing agent

Romain Ruppert,   Christophe Jeandon,   Anna Sgambati  and  Henry J. Callot  

Abstract

Electrochemical or Na2S2O4 reduction of N-arylporphyrins gives stable phlorins epimeric to those obtained by tosylhydrazine or NaBH4 reduction.

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Article information

DOI
https://doi.org/10.1039/A905676I
Article type
Paper

Chem. Commun., 1999, 2123-2124

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Reduction of N-arylporphyrins to N-arylphlorins: opposite stereochemical courses as a function of the reducing agent

R. Ruppert, C. Jeandon, A. Sgambati and H. J. Callot, Chem. Commun., 1999, 2123 DOI: 10.1039/A905676I

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