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Alcoholysis nucleophilic acyl substitution

To begin with, it seems very likely that chymotrypsin acts in two stages. In the first stage, acting as an alcohol, it breaks the peptide chain. We recognize this as alcoholysis of a substituted amide nucleophilic acyl substitution. The products are an amine—the liberated portion of the substrate molecule—and, as we shall... [Pg.1165]


See other pages where Alcoholysis nucleophilic acyl substitution is mentioned: [Pg.55]    [Pg.574]    [Pg.101]    [Pg.101]    [Pg.459]    [Pg.2]    [Pg.199]    [Pg.2522]    [Pg.422]   


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