Publisher
Florida Atlantic University
Description
In this research it was found that strongly
nucleophilic aromatic compounds, like phenol, resorcinol,
anisole, N,N-dimethylaniline, mes.l.tylene, thiophene,
thianaphthene, N-methylpyrrole, indole and ferrocene, are
ferrocenylmethylated on a ring-carbon by (ferrocenylmethyl)-
trimethylammonium iodide. The ferrocenylmethylation of aniline, N-methylaniline
and acetanilide yielded N-, o- and p-ferrocenylmethylated
products. The N-ferrocenylmethylated compounds have been
shown to undergo acid catalyzed intermolecular rearrangements
to their corresponding o- and p-ferrocenylmethyl
isomers. NMR was especially useful in structure analysis.
Note
Thesis (M.S.)--Florida Atlantic University, 1972.
Extension
FAU
FAU
admin_unit="FAU01", ingest_id="ing1508", creator="staff:fcllz", creation_date="2007-07-19 01:09:14", modified_by="staff:fcllz", modification_date="2011-01-06 13:08:48"
Person Preferred Name
PENNIE, JOHN THOMAS.
Graduate College
Title Plain
FERROCENYLMETHYLATION OF AROMATIC COMPOUNDS
Use and Reproduction
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Physical Location
Florida Atlantic University Libraries
Title
FERROCENYLMETHYLATION OF AROMATIC COMPOUNDS
Other Title Info
FERROCENYLMETHYLATION OF AROMATIC COMPOUNDS