Examples of 'amino protecting group' in a sentence
Meaning of "amino protecting group"
Amino protecting group : In chemistry, an amino protecting group is a molecular structure that is used to temporarily mask or protect the amino group of an organic molecule during chemical reactions, preventing unwanted reactions at that site
How to use "amino protecting group" in a sentence
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amino protecting group
Example of such an amino protecting group is acetyl.
An amino protecting group that can be used is a benzoyl group.
X may be hydrogen or a hydroxlyzable amino protecting group.
A preferred amino protecting group is carbobenzoxy.
This step is optional before removing the amino protecting group.
A preferred amino protecting group is trityl.
The reaction conditions depend on nature of the amino protecting group.
The amino protecting group is acceptable in the art.
Y may be any suitable amino protecting group.
The amino protecting group may then be removed by conventional procedures.
Is hydrogen or an amino protecting group and.
Said amino protecting group is removed after completion of the esterification.
P represents a suitable amino protecting group.
Examples of cyclic amino protecting group are phthaloyl group and nitrophthaloyl group.
This protection can be by means of any conventional amino protecting group.
See also
Another suitable amino protecting group is a carbobenzoxy group.
Hydroxy or amino groups may be protected with any hydroxy or amino protecting group.
A particularly suitable amino protecting group is the allyloxycarbonyl group.
The reaction conditions for the deprotection depend on the amino protecting group used.
It should be understood that an amino protecting group may remain on an end product.
The amino protecting group used in this step is not particularly limited.
Is a hydrogen or an amino protecting group.
Virtually any amino protecting group can be used to put the invention into practice.
Wherein R is an amino substituted by an amino protecting group.
Introduction of the amino protecting group is known to the skilled in the art.
A compound of the structure wherein P is an amino protecting group.
Preferably the amino protecting group is cleaved off prior to the next coupling step.
In certain embodiments, the substituent present on the nitrogen atom is an amino protecting group.
Each amino protecting group can be attached using techniques well known in the art.
Each PG independently refers to an amino protecting group such as phthalamide.
The amino protecting group can be any suitable protecting group known to the skilled person.
Wherein PG is an amino protecting group.
The amino protecting group can be any conventional amino protecting group utilized in peptide synthesis.
Again, the preferred amino protecting group is phthalimido.
An amino protecting group is preferably t-butoxycarbonyl or benzyloxycarbonyl.
A process according to claim 11 wherein the amino protecting group is an acetyl or an aryloxycarbonyl.
The amino protecting group in adenine, guanine and cytosine was removed from the oligomer.
Following the above reaction, the amino protecting group is removed by known procedures.
The 7-amino group of the cephalosporin is optionally protected with a conventional amino protecting group.
Preferably the amino protecting group is metyl carbamate or CBZ.
In step b - protection of the amino group, any suitable amino protecting group may be used.
Preferable Pro is amino protecting group which can be removed under the acid condition.
The free nitrogen of the piperidine moiety is protected with an amino protecting group PG2.
A preferable amino protecting group is para-methoxybenzyl.
In one embodiment, Y is a suitable amino protecting group.
The preferred amino protecting group is tert-butyloxycarbonyl.
X is oxygen or nitrogen ; and is H or an amino protecting group.
A preferred amino protecting group is t - butyloxycarbonyl.
In 2 the group R denotes an amino protecting group.
If required, the amino protecting group can be removed group following general synthetic method 5.
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