Examples of 'hydrolysis of the ester' in a sentence
Meaning of "hydrolysis of the ester"
hydrolysis of the ester - This phrase is used in chemistry to describe a chemical reaction in which an ester compound is broken down into its constituent molecules by the addition of water. It involves the cleavage of the ester bond, resulting in the formation of an alcohol and a carboxylic acid
How to use "hydrolysis of the ester" in a sentence
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hydrolysis of the ester
Hydrolysis of the ester group of b yields acid c.
A base is used in the hydrolysis of the ester groups.
The hydrolysis of the ester may be carried out in an acidic or basic medium.
The reaction proceeds together with hydrolysis of the ester.
Selective hydrolysis of the ester.
Such polyesters liberate the peptide in vivo by hydrolysis of the ester bond.
Conventional hydrolysis of the ester produces the half acid.
The conditions employed during some of the stages cause hydrolysis of the ester.
Simple alkaline hydrolysis of the ester functionality provides the acidic junction.
Human insulin is produced through transpeptidation followed by hydrolysis of the ester bond formed.
Base hydrolysis of the ester to the acid was followed by coupling of a sulfonamide derivative.
Hydrolysis of the phospholipids refers to hydrolysis of the ester bond of the phospholipid.
Hydrolysis of the ester and treatment with thionyl chloride provides the desired acid chloride.
At this time TLC indicated that the hydrolysis of the ester was complete.
Simple alkaline hydrolysis of the ester functionality provides the acidic function.
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Amino pyrazole intermediates of this invention can be obtained by hydrolysis of the ester 2b.
After mild basic hydrolysis of the ester will give the desired amidino carboxylic acids.
Copper-catalyzed Ullmann coupling reaction followed by hydrolysis of the ester produces the compounds Ib.
Hydrolysis of the ester under basic conditions provides the pyrazole acid intermediate XVII.
In addition, the water content accelerates the hydrolysis of the ester oil, thus forming sludge.
Hydrolysis of the ester group in the resultant linked product C generates the target compound.
Deprotection to the aniline followed by hydrolysis of the ester in C3 gives acid C4.
Further hydrolysis of the ester LXI gives compound Io.
The incubation is carried out at pH 7.0 to minimise spontaneous hydrolysis of the ester bond.
Hydrolysis of the ester LXXV gives the compound of interest Iu.
Also, the carbomethoxyanilides 1d and 1e undergo cyclization without subsequent hydrolysis of the ester function.
Selective alkaline hydrolysis of the ester group of compounds V yielded the corresponding secondary alcohols VI.
Purification was performed by crystallization followed by hydrolysis of the ester to the A-9-tetrahydrocannabinol.
Base hydrolysis of the ester of Formula XII forms the carboxylic acid of Formula XIII.
The final product ( 34 mg ) was obtained after NaOH hydrolysis of the ester.
Hydrolysis of the ester of a compound of the formula,.
Reduction of the double bond and hydrolysis of the ester affords acid 21-4.
Basic hydrolysis of the ester grouping then affords 7.
Subsequent catalytic reduction of Compound 5.1 and hydrolysis of the ester yields DCA ( Scheme 5 ).
Followed by hydrolysis of the ester to form a compound of formula,.
Hydrolysis of the ester affords the pyrazole acids 4f.
Followed by the hydrolysis of the ester of racemic thioctic acid ;.
Hydrolysis of the ester affords the pyrazole acids 4d.
Preferably, the hydrolysis of the ester group is catalyzed by base or acid.
Hydrolysis of the ester with either trifluoroacetic acid or NaOH affords carboxylic acid 21.
In the final step hydrolysis of the ester groups gives the anti-diol.
Hydrolysis of the ester group follows a triple mechanism, resulting in an acid and a base.
Stage 2 requires the hydrolysis of the ester group to form the corresponding acid.
Hydrolysis of the ester with aqueous lithium hydroxide as described previously gives the acid 1b.
Stage c, hydrolysis of the ester.
Hydrolysis of the ester and removal of the amine protecting group affords amino acids 23.
Thereafter, hydrolysis of the ester moieties was made using trifluoro acetic acid.
Hydrolysis of the ester and subsequent conversion into the hydroxamic acid then provides compounds 1.
Acid hydrolysis of the ester obtained in step ( i ).
Hydrolysis of the ester and reaction with hydroxylamine hydro-chloride would then give the invention compound.
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Are obtained immediately after hydrolysis of inulin or oligofructose
Hydrolysis is an important reaction controlling abiotic degradation
Thus photolysis and hydrolysis are not significant
Examples of using Ester
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The ester pentachlorophenyl laurate was used in textiles
It is an analogous dimethyl ester and an organothiophosphate acaricide
Ester did not have a mass in her heart
