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Mechanism of enzyme catalysis.

Mechanism of enzyme inactivation at an aqueous-organic interface. Step 1

Mechanism of enzyme inactivation by 7-amino-4-chloroisocoumarins .

Mechanism of enzyme inactivation by peptide chloromethyl ketones.

Mechanism of enzyme inactivation by phosphofluoridates.

Mechanism of enzyme inactivation by yS-lactam inhibitors.

Mechanism of enzyme inhibition by aldehydes.

Mechanism of enzyme inhibition by benzoxazinones .

Mechanism of enzyme inhibition by saccharin based inhibitors. Only if R contains a leaving group, eg. , does the inhibitor progress to a dicovalently linked enzyme.

Mechanism of enzyme-catalyzed organophosphate hydrolysis.

Mechanism of epoxidation by a chiral ketone catalyst.

Mechanism of epoxidation of 6p-hydroxyhyoscyamine.

Mechanism of epoxidation using a manganese complex.

Mechanism of epoxidation using diethylzinc and methylpseudoephedrine.

Mechanism of epoxidation using titanium chiral complex.

Mechanism of epoxide formation from a halohydrin.

Mechanism of epoxide opening by azides

Mechanism of epoxide opening through direct ET

Mechanism of ester bond formation via O-acylisourea.

Mechanism of ester hydrolysis

Mechanism of ester hydrolysis by Breslow s system consisting of two cyclodextrins appended to a mononuclear Cu complex.

Mechanism of ester hydrolysis by yS-cyclodextrin.

Mechanism of ester hydrolysis in acidic media.

Mechanism of ester hydrolysis involves a high energy tetrahedral intermediate. Phos-

Mechanism of ester hydrolysis involves a high energy tetrahedral intermediate. Phosphonates accurately mimic this intermediate and can be used as haptens to induce catalytic antibodies for ester hydrolysis



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