The regiospecific p-deiodination of 2,4-di-iodo phenols; a new synthesis of aflatoxin B2
Abstract
An o-iodinated phenolic tetrahydrofurobenzofuran intermediate has been prepared with the correct regiochemistry and converted into aflatoxin B2.
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Article information
- Article type
- Paper
J. Chem. Soc., Chem. Commun., 1990, 39-41
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The regiospecific p-deiodination of 2,4-di-iodo phenols; a new synthesis of aflatoxin B2
S. Horne, G. Weeratunga and R. Rodrigo, J. Chem. Soc., Chem. Commun., 1990, 39 DOI: 10.1039/C39900000039
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