Examples of 'deprotonation' in a sentence
Meaning of "deprotonation"
Deprotonation (noun): Deprotonation is a chemical process where a proton is removed from a molecule, resulting in the formation of a conjugate base. It is a fundamental concept in acid-base reactions and organic chemistry
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- The removal of a proton (hydrogen ion) from a molecule to form a conjugate base.
How to use "deprotonation" in a sentence
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deprotonation
Deprotonation of a carboxyl group gives a carboxylate anion.
Instead the extent of deprotonation is expected to decrease.
Deprotonation of dimethylamine can be effected with organolithium compounds.
Basic ether cleavage is induced by deprotonation in α position.
Simple deprotonation affords the pure enantiomer.
Moreover it is sensitive to the deprotonation of its imide function.
Through a deprotonation reaction or some other modification.
A carboxylate can be easily made by deprotonation of carboxylic acids.
Deprotonation of acetic acid by a hydroxide ion.
It is the product of deprotonation of formic acid.
The deprotonation may be accomplished using an appropriate base.
The base functions as a deprotonation agent.
Deprotonation typically increases the reactivity of the nucleophiles.
This leads to substantial deprotonation of the accumulated ionizable lipid.
Deprotonation appear to be partially reversed when washed in acid.
See also
Azomethine ylides can also be formed directly by deprotonation of iminiums.
Deprotonation was allowed to proceed at room temperature.
A base can be used to facilitate the deprotonation of the phenol.
Deprotonation of sigma complex to restore aromaticity.
Acid boronates have a stoichiometry consistent with single deprotonation.
Deprotonation triggers water entry to the binding sites.
A preferred strong base for the deprotonation reaction is lithium diisopropylamide.
Deprotonation reactions can be varied within a relatively wide range.
It has not been determined if deprotonation occurs prior to or after oxygen coordination.
Deprotonation of the carbocation.
These ions undergo efficient cyclization and deprotonation to give benzothiophenes.
This deprotonation step is the driving force for this reaction.
The conjugate base resulting from deprotonation of the amine is rarely observed.
Deprotonation by strong bases.
The carbon atom at which the initial deprotonation takes place is a stereocenter.
Deprotonation of the radical was dependent on the concentration of water as proton acceptor.
It is appreciated that more than one deprotonation or protonation event may occur.
Deprotonation occurs on the amine groups of the hydrogel network at high pH.
Any sufficiently strong base can be used for the initial deprotonation.
Kinetic controlled deprotonation requires a base that is sterically hindered.
It is also soluble in strongly alkaline aqueous solutions due to deprotonation of the phenol.
The anion produced by deprotonation of the alcohol group is known as benzylate or benzyloxide.
The diazomethane is a very reactive source of methyl after deprotonation of the acid.
This deprotonation plays a role in the reduction of the pendant ester group.
Both of these reactions are carried out in a basic medium with a deprotonation agent.
Deprotonation by pyridine.
The overall reaction sequences are known as the deprotonation grafting reaction of this invention.
Deprotonation of tropinone with chiral lithium amides proceeded with modest enantioselectivity.
The same phenomenon was observed for the anilide complex obtained through deprotonation.
The extent of deprotonation may vary according to the environment of the complex.
The initial stages in the reaction appear to involve deprotonation of the isothiazolium salt.
Deprotonation by water.
Z must be powerful enough to facilitate deprotonation to the enolate ion even with a mild base.
The deprotonation of carbon acids can proceed with either kinetic or thermodynamic reaction control.
Loss of water from this oxonium ion and subsequent deprotonation gives the ester.
