Examples of 'deprotection' in a sentence
Meaning of "deprotection"
Deprotection is a term used in organic chemistry that refers to the removal of protecting groups from functional groups to expose them for further reactions
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- The removal of a protecting group when it is no longer needed.
How to use "deprotection" in a sentence
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deprotection
Total deprotection of the compound obtained in step g.
This step can be performed by general deprotection.
Deprotection of the imidazoles of the copolymer polyE.
It was assumed that the deprotection had gone to completion.
The deprotection is carried out as mentioned above.
The glycosylation may occur before deprotection.
This deprotection may be carried out by hydrolysis.
Acidic or basic hydrolysis will provide deprotection.
This deprotection is carried out in a conventional manner.
The process of the invention is a deprotection reaction.
The deprotection is carried out as indicated above.
Fmoc groups are subsequently removed by deprotection methods.
Cleavage and deprotection of support bound oligomer.
It is used in the fluorination of steroids and in deprotection of peptides.
Side chain deprotection and cleavage reaction.
See also
The expected compound is obtained after a deprotection step.
After deprotection the desired product is obtained.
In such a case a subsequent deprotection step will be necessary.
Deprotection if necessary results in the desired compound.
An example of the deprotection of glucose is shown below.
Deprotection may be performed under standard conditions.
At present a better method of deprotection and complexation is being explored.
Final deprotection of this peptide was accomplished by saponification.
This may be followed by deprotection of the protecting groups.
Deprotection can provide the complete subunit.
Several routes for deprotection of the carbonyl are possible.
Deprotection would lead to the final compounds.
Standard protection and deprotection techniques can be used.
Deprotection using hydrazine is described in the examples.
Any suitable acidic deprotection reaction may be performed.
Deprotection then gives a compound of the invention.
Fluoride mediated deprotection of silyl ethers.
The deprotection is carried out by means known per se.
This is a very mild deprotection condition.
Final deprotection and cleavage off resin.
The free oxyamine is generated by deprotection in basic medium.
Optional deprotection to release the free thiol.
The synthesis reaction may be a coupling or deprotection reaction.
Subsequent deprotection results in a compound of formula XVa.
The polymer can be hydrogenated before or after deprotection.
Subsequent deprotection provides a compound of the invention.
In some instances a final standard deprotection step was required.
Global deprotection afforded the desired hexamer.
A colorimetric test is conducted to ensure deprotection.
Subsequent deprotection gives the desired ketone.
This step is often referred to as deprotection.
Selective deprotection of silyl groups is possible in many instances.
Conventional methods of deprotection may be used.
Deprotection can be carried out by hydrogenolysis.
Is added to the neutralized deprotection mixture at room temperature.
