| 1. | This occurs even if the equivalents of nucleophile are closely controlled.
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| 2. | ATase is the only PRTase that has ammonia as a nucleophile.
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| 3. | This is followed by a rapid reaction with the nucleophile.
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| 4. | The nucleophile will attack the mercurinium ion at this time.
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| 5. | With a sterically hindered, making it a weak nucleophile.
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| 6. | The second nucleophile is methylmagnesium bromide expulsing the pyrazole group.
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| 7. | This strong nucleophile can then be used as such with other electrophiles.
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| 8. | Which is a better nucleophile, OH-or NH3?
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| 9. | The chiral ketene enolate nucleophile attacks electrophilic carbon of the imine group.
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| 10. | Here, sodium amide is used as the nucleophile yielding 2-aminopyridine.
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