Issue 21, 1989

The mechanism of biological C–C bond formation to methoxy groups; biomimetic cyclisation via alkyloxyl radicals

Abstract

Aryl(methylene)oxyl radicals generated by decarboxylation of the thiohydroxamate ester (8) undergo 6-endo cyclisation, yielding ketones (9) and (11), mimicking an unusual biosynthetic conversion.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1989, 1613-1615

The mechanism of biological C–C bond formation to methoxy groups; biomimetic cyclisation via alkyloxyl radicals

S. A. Ahmad-Junan, A. J. Walkington and D. A. Whiting, J. Chem. Soc., Chem. Commun., 1989, 1613 DOI: 10.1039/C39890001613

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