Issue 15, 1971

Activation of electrophilic aromatic substitution by a methyleneiron carbonyl substituent

Abstract

Deuteriation of the aromatic ring of benzyldicarbonyl-π-cyclopentadienyliron occurs more readily than does the deuteriation of anisole under comparable conditions; i.e., the group –CH2Fe(CO)2π-C5H5 is more highly activating than is the methoxy-group in aromatic electrophilic substitution.

Article information

Article type
Paper

J. Chem. Soc. D, 1971, 779-780

Activation of electrophilic aromatic substitution by a methyleneiron carbonyl substituent

S. N. Anderson, D. H. Ballard and M. D. Johnson, J. Chem. Soc. D, 1971, 779 DOI: 10.1039/C29710000779

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