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Pinacol-type epoxide ring

Although hydroxylation of phenylalanine to tyrosine looks like a typical electrophilic aromatic substitution, scientists at the U.S. National Institutes of Health discovered that the biochemical pathway combines epoxidation of the benzene ring followed by epoxide ring-opening with rearrangement. This rearrangement, which is the biochemical analog of the pinacol-type reactions described earlier, is known as the NIH shift. ... [Pg.722]


See other pages where Pinacol-type epoxide ring is mentioned: [Pg.466]    [Pg.466]    [Pg.1127]    [Pg.787]    [Pg.158]    [Pg.434]    [Pg.286]    [Pg.6580]    [Pg.6579]    [Pg.510]    [Pg.645]    [Pg.144]    [Pg.116]    [Pg.126]    [Pg.654]   


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Pinacol

Pinacolate

Pinacolation

Pinacolizations

Pinacols

Ring epoxides

Ring type

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