Examples of 'azides' in a sentence
Meaning of "azides"
azides (noun) - chemical compounds containing the N3- ion, commonly used in organic synthesis and pharmaceuticals
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- plural of azide
How to use "azides" in a sentence
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azides
Organic azides engage in useful organic reactions.
Process for the preparation of organic azides.
The dominant application of azides is as a propellant in air bags.
Acyl azides are used as chemical reagents.
It is one of the prototypical organic azides.
Photolysis or thermolysis of azides are good ways to generate nitrenes.
Azides of various protecting groups.
Alkali metal azides may be used.
It is used to make other azides.
Such heavy metal azides are explosive in dry form.
Dipolar cycloaddition with azides.
Acyl azides are in this category.
Propellants containing azides are poisonous.
The azides were reduced using the tin reagent described above.
Inflators containing azides.
See also
Low molecular weight azides are considered especially hazardous and are avoided.
This method is a variation on nitrogen expulsion in azides with formation of a nitrene.
Preparation of the composition of the present invention using aryl azides.
Reaction of organic azides with metal carbenoids produced from diazocarbonyl compounds.
Salts of inorganic acids or peroxoacids excluding azides and double or complex silicates.
Some azides are produced by treating the carbonate salts with hydrazoic acid.
Suitable examples of such phosphoryl azides may for example be diphenylphosphoryl azide.
Azides IIbb can be prepared by reaction of amides IIba with sodium azide.
According to the invention the azides can contain any electron acceptor groups.
Used in conjunction with NaI in acetonitrile to mildly reduce organic azides to primary amines.
Polyglycidyl azides comprising an acyloxy terminal group and an azide terminal group.
One reason is that the isonitrile oxides are typically less stable than azides.
Alkali metal azides or alkali metal cyanides can be used in this reaction stage.
Additional hydroxyl functionality is envisioned through use of propanediol or glycerol based aliphatic azides.
Examples of suitable alkali metal azides include sodium azide and lithium azide.
Aryl azides conjugated to oligomers will effect crosslinking with nucleic acids and proteins upon irradiation.
Acyl chlorides condense with vinyl azides in the presence of aluminum chloride to yield oxazoles.
Amines Law can be prepared by hydrogenation of azides IIbb.
Especially preferred azides are those as mentioned in the Examples.
The Curtius Rearrangement is the thermal decomposition of carboxylic azides to produce an isocyanate.
Aryl azides conjugated to PNA will effect crosslinking with nucleic acids and proteins upon irradiation.
Reactions with Azides.
The required azides LXXXIX are readily available.
Other salts of inorganic acids or peroxoacids, excluding azides.
However, the azides and alkynes are both kinetically stable.
Of these, we prefer the diarylphosphoryl azides.
However, sulfonyl azides and other azides can be shock sensitive.
By proper choice of reactions, it is possible to obtain either of the stereoisomeric azides.
Typically, alkali or tetraalkyl azides are used as a common source for azide.
Such azides are not ideal, since they can be dangerously unstable.
Some acyl, sulfonyl and pyridyl azides are also commercially available.
Azides commonly used are alkaliazides like sodium azide in amounts of 1 to 2 equivalents.
Figure 3 depicts a common synthetic route for the preparation of azides.
Dye sulfonyl azides are for example also used in dyeing processes e . g.
The traditional photo-reactive groups in these reagents are aryl azides.
