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Electrophilic aromatic substitution reactions epoxide substrate

The high-valent iron-oxo sites of nonheme iron enzymes catalyze a variety of reactions (halogenation and hydroxylation of alkanes, desaturation and cyclization, electrophilic aromatic substitution, and cis-dihydroxylation of olefins) [lb]. Most of these (and other) reactions have also been achieved and studied with model systems [Ic, 2a-c]. With the bispidine complexes, we have primarily concentrated on olefin epoxidation and dihydroxylation, alkane hydroxylation and halogenation, and sulfoxidation and demethylation processes. The focus in these studies so far has been on a thorough analysis of the reaction mechanisms rather than the substrate scope and catalyst optimization. [Pg.132]


See other pages where Electrophilic aromatic substitution reactions epoxide substrate is mentioned: [Pg.259]    [Pg.259]    [Pg.376]    [Pg.602]    [Pg.107]    [Pg.259]    [Pg.150]    [Pg.150]    [Pg.241]    [Pg.259]   
See also in sourсe #XX -- [ Pg.7 ]




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Aromaticity electrophilic aromatic substitution

Aromatics electrophilic substitution

Electrophile Electrophilic aromatic substitution

Electrophile reactions Electrophilic aromatic

Electrophiles epoxides

Electrophilic aromatic reactions

Electrophilic substitution reaction

Epoxide reaction

Epoxides reactions

Epoxides substituted

Epoxides substrates

Reactions aromatic substrates

Reactions epoxidation

Substitution electrophilic aromatic

Substitution electrophilic aromatic substitutions

Substitution reactions aromatic

Substitution reactions electrophile

Substitution reactions electrophilic aromatic

Substitution reactions substrate

Substrate reaction

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