Examples of 'isomers can' in a sentence
Meaning of "isomers can"
isomers can: This phrase is used to suggest the ability or potential of isomers in a chemical context. It implies that isomers have the capability to exhibit certain properties or reactions
How to use "isomers can" in a sentence
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isomers can
The isomers can be separated by gas chromatography.
Several positional isomers can be distinguished.
Isomers can be prepared using conventional methods.
Mixtures of any of the isomers can also be used.
The isomers can be separated by gas chromatographic methods.
A pure butene or a mixture of butene isomers can also be introduced.
The isomers can be separated by methods known per se.
In case mixtures of isomers are obtained these isomers can be separated by chromatography.
Geometric isomers can exist in the present compounds.
With other starting materials the respective isomers can be obtained.
Optical isomers can be produced by a per se known method.
Both racemic mixtures and optically active isomers can be used as precursors.
The individual isomers can be obtained by chromatographic separation.
What follows looks at some of the ways that structural isomers can arise.
The two isomers can than be readily separated.
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Under optimized conditions the formation of mainly one of the two isomers can be achieved.
The various isomers can be obtained by standard methods.
In the present invention, either of the isomers can be employed.
The ratio of the isomers can be adjusted by controlling pH.
If desired, subsequently separation of the optical isomers can take place.
Both optical isomers can thus be selectively prepared.
Furthermore, the pharmacological activity of the two isomers can differ considerably.
The isomers can be resolved by methods known per se.
The isomeric ratio of MDI isomers can vary in wide ranges.
Such isomers can also be isolated by resolving racemic mixtures.
Certain oligosaccharide isomers can be resolved using HPAEC.
Other isomers can be obtained by appropriate use of blocking groups.
Accordingly, any isomers can be included.
These isomers can be separated by any known separation method.
Piperine metabolites, analogues and isomers can be prepared synthetically.
The two isomers can then be readily separated.
In the present invention, all these optically active isomers can be used.
Related isomers can have very different effects.
When available, the corresponding isomers and optical isomers can be used.
The two isomers can be separated by silica gel chromatography.
When optically active starting materials are used, pure diastereomers and optical isomers can be obtained.
All of the isomers can be employed in the present invention.
The separation of the diastereoisomers and / or optical isomers can be effected by known methods E.
The isomers can be separated according to methods known per se.
The equilibrium between conformational isomers can be observed using a variety of spectroscopic techniques.
Isomers can be separated at this step or at a later step in the process.
The entire set of geometrical isomers can be prepared in the laboratory by photolysis.
The isomers can be separated using art recognized techniques such as crystallization or chromatography.
Naturally occurring or synthetic isomers can be separated in several ways known in the art.
These isomers can be isolated by a conventional method or produced by using various starting compounds.
Each of the cis and trans isomers can have two optical configurations.
These isomers can be separated into individual components by conventional means.
For instance, non-limiting examples of octyl isomers can include 2-ethyl hexyl and neooctyl.
Such isomers can be used as active ingredient compounds as well.
In the compounds of formula ( I ) cis-trans type isomers can also be present.
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