nucleophile การใช้
- This occurs even if the equivalents of nucleophile are closely controlled.
- ATase is the only PRTase that has ammonia as a nucleophile.
- This is followed by a rapid reaction with the nucleophile.
- The nucleophile will attack the mercurinium ion at this time.
- With a sterically hindered, making it a weak nucleophile.
- The second nucleophile is methylmagnesium bromide expulsing the pyrazole group.
- This strong nucleophile can then be used as such with other electrophiles.
- Which is a better nucleophile, OH-or NH3?
- The chiral ketene enolate nucleophile attacks electrophilic carbon of the imine group.
- Here, sodium amide is used as the nucleophile yielding 2-aminopyridine.
- In humans, the nucleophile of the hydrolysis reaction is Glu-268.
- First it acts as a general base to activate water as a nucleophile.
- The first equivalent of nucleophile acts as a base and deprotonates the acid.
- Here, a prenyl ester serves as both the nucleophile and electrophile precursor.
- This observation is most often noted when the base is also a nucleophile.
- Is it because it's a good nucleophile?
- The electrophiles are attacked by the most electron-populated part of one nucleophile.
- For families are designated by their catalytic nucleophile ( S = serine proteases ).
- The reaction makes use of phloroglucinol as nucleophile.
- For families are designated by their catalytic nucleophile ( C = cysteine proteases ).
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