Examples of 'nitrogen protecting' in a sentence

Meaning of "nitrogen protecting"

Nitrogen protecting - Refers to the process of using nitrogen gas as a protection method in industries like welding, food packaging, electronics to prevent oxidation

How to use "nitrogen protecting" in a sentence

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nitrogen protecting
Most preferred nitrogen protecting group is benzyl.
Nitrogen protecting groups are well known in the art.
When present is hydrogen or a nitrogen protecting group.
Q is a nitrogen protecting group.
The tetrazoles and triazoles are optionally protected with a nitrogen protecting group.
A preferred nitrogen protecting group is benzyl.
Certain intermediates described in the following preparations may contain one or more nitrogen protecting groups.
Of course any operable nitrogen protecting group is included.
Nitrogen protecting groups useful for this reaction are well known to the skilled artisan.
Examples of typical nitrogen protecting groups are described below.
Nitrogen protecting groups can be used for protecting amine groups present in the described compounds.
Examples of typical nitrogen protecting groups are described above.
Nitrogen protecting groups Nitrogen protecting groups are well known in the art.
Suitable examples of imidazole nitrogen protecting groups include tetrahydropyranyl.
In certain aspects of the present disclosure, carbamates are used as nitrogen protecting groups.

See also

Pg is a suitable nitrogen protecting group.
Nitrogen protecting groups, as well as protection and deprotection methods are known in the art.
Several well known nitrogen protecting groups can be used.
Additionally, the intermediates described in the following schemes contain a number of nitrogen protecting groups.
In situ cleavage of the benzoyl nitrogen protecting group was observed.
PG is a nitrogen protecting group such as CBz or boc.
PG is selected from suitable nitrogen protecting groups.
Other suitable nitrogen protecting groups and nitrogen protecting group reagents are disclosed in Greene.
Is an appropriate enzyme labile nitrogen protecting group ;.
Removal of the nitrogen protecting group provides the required Formula III intermediate.
Is an appropriate photolabile nitrogen protecting group ;.
Exemplary nitrogen protecting groups include carbobenzyloxy or t-butoxycarbonyl.
In certain other exemplary embodiments, nitrogen protecting groups are utilized.
G is a nitrogen protecting group or hydrogen ;.
After the alkylation reaction has been completed, the nitrogen protecting group is removed.
A preferred nitrogen protecting group is Fmoc.
The term " protected amino " refers to a primary or secondary amine having a nitrogen protecting group.
Removal of the trifluoroacetyl nitrogen protecting group yields the desired compound of the formula IE.
Additionally, the formation of such salts can occur concomitantly with deprotection of a nitrogen protecting group.
Removal of the trifluoroacetyl nitrogen protecting group yields the desired compound of the formula IG.
The oxazolidine may be hydrolyzed back to the nor-compound so could act a nitrogen protecting group.
Protecting the azetidine nitrogen with a nitrogen protecting group P to form a compound of the formula.
Additionally, the formation of such salts can occur simultaneously upon deprotection of a nitrogen protecting group.
The preferred nitrogen protecting group is BOC.
Nitrogen protecting group ( Prot ) means a group capable of protecting a nitrogen from a reaction.
PG refers to a suitable nitrogen protecting group such as BOC.
The nitrogen protecting group Q is preferably a trifluoroacetyl group or a t - butoxy carbonyl group.
Removal of the nitrogen protecting group ;.
Also, the process of the present invention is carried wherein R2 is a nitrogen protecting group.
Preferably, the nitrogen protecting group is benzyloxycarbonyl.
The process of claim 1 further comprising removing the nitrogen protecting group P.
Removal of the nitrogen protecting group e . g.
Pyrazole 77 is obtained by removal of the pyrazole nitrogen protecting group.
When the nitrogen protecting group is no longer needed, it may be removed.
Diastereoselectivity of this reaction depends on the nitrogen protecting group, and on the imine substituent.

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