Publisher
Florida Atlantic University
Description
The ferrocenylrnethylation of the following compounds was studied
using (ferrocenylmethyl)trimethylammonium iodide: 1, 1-di(p-anisyl)-
ethene (I), 1, 1-di(p- anisyl)propene (II), 1- (p- anisyl)-1-phenylethene
(III), 1, 1- diphenylethene (IV), 1, 1- di(p- dimethylaminophenyl )ethene
(V) and 1, 1-di(p-dimethylaminophenyl)propene (VI). I is ferrocenylmethylated
exclu,sively on its side-chain, one or both vinyl hydrogens
being replaced by ferrocenylmethyl groups depending on the ratio of
ferrocenylmethylating agent to I, concentration of the reaction mixture,
reaction time, solvent and temperature. II is substituted only on its
side-chain to give a mono-ferrocenylmethylated product. III is ferrocenylmethylated
slowly. IV fails to react. Mono-ferrocenylmethylation
of V occurs principally on its side- chain; more extensive ferrocenylmethylation
occurs both on the side-chain and on the rings at the
position ortho to dimethylamino. VI reacts quite indiscriminately both
on the side-chain and on the rings.
Note
Thesis (M.S.)--Florida Atlantic University, 1977.
Extension
FAU
FAU
admin_unit="FAU01", ingest_id="ing1508", creator="staff:fcllz", creation_date="2007-07-19 01:42:09", modified_by="staff:fcllz", modification_date="2011-01-06 13:09:05"
Person Preferred Name
FERNANDEZ, ROSA MIRTA
Graduate College
Title Plain
FERROCENYLMETHYLATION OF 1,1-DIARYLALKENES
Use and Reproduction
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Physical Location
Florida Atlantic University Libraries
Title
FERROCENYLMETHYLATION OF 1,1-DIARYLALKENES
Other Title Info
FERROCENYLMETHYLATION OF 1,1-DIARYLALKENES