Examples of 'enantiomers can' in a sentence
Meaning of "enantiomers can"
Enantiomers can: This phrase refers to a type of chemical compound that has mirror-image structures but are not superimposable. They are important in the field of chemistry and pharmacology for their different effects on biological systems
How to use "enantiomers can" in a sentence
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enantiomers can
Enantiomers can be separated by chiral chromatographic columns.
Chromatographic resolution of enantiomers can be accomplished on chiral chromatography resins.
Enantiomers can have one or more stereocenters.
Number of stereocentres enantiomers can have one or more stereocenters.
Enantiomers can be mentioned as an example of isomers.
The salts of the sulfoxide enantiomers can be prepared by conventional means.
Enantiomers can also be separated by classical resolution techniques.
Any separation into diastereoisomers and enantiomers can be carried out by conventional methods.
The enantiomers can be separated by silica column chromatography.
Once the diastereomers are separated by chromatography, the individual enantiomers can be regenerated.
Unnatural enantiomers can also be used.
Under the most suitable conditions, complete baseline separation of both enantiomers can be observed.
The enantiomers can be separated using chiral chromatography.
The ratio, the purity, and the concentration of two enantiomers can be measured via polarimetry.
Preferred enantiomers can also be prepared by asymmetric syntheses.
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The bioavailability of S ( + ) ketoprofen and other S ( + ) enantiomers can also be determined using this protocol.
The enantiomers can be prepared through stereoselective synthetic process.
Individual diastereoisomers or individual enantiomers can also be obtained by Supercritical Fluid Chromatography ( SCF ).
Such enantiomers can be used to prevent unwanted angiogenesis in a human or animal.
Alternatively, the single enantiomers can be prepared by an asymmetric synthesis.
Enantiomers can also be directly separated using chiral chromatographic techniques.
Resolution of 1 into its enantiomers can be achieved through chiral HPLC.
The enantiomers can be obtained by resolution of the racemates according to known methods.
Alternatively, both individual enantiomers can be isolated or synthesized by conventional techniques if so desired.
The enantiomers can be separated by conventional techniques known in the art.
Separation of enantiomers can be carried out at any of several steps.
Enantiomers can also be separated by use of chiral HPLC column.
Said individual enantiomers can be separated by means of conventional techniques.
Enantiomers can also be separated by use of a commercially available chiral HPLC column.
In some cases, enantiomers can have opposite pharmacological effects.
Enantiomers can then be separated by HPLC.
In one embodiment, enantiomers can be separated by chiral chromatographic columns.
Enantiomers can be produced using various techniques e . g.
Mixtures of the different enantiomers can be called catechin or DL-catechin and epicatechin or DL-epicatechin.
Enantiomers can also be separated by use of a chiral HPLC ( high pressure liquid chromatography ) column.
Alternatively, the enantiomers can be separated following conversion to Formula I.
Enantiomers can also be separated, for example, by use of chiral HPLC column.
The individual enantiomers can be separated by resolution of the racemate by classical methods.
The enantiomers can also be prepared by separation via chiral phase chromatography.
Diastereoisomers and enantiomers can be separated by conventional techniques such as chromatography or fractional crystallization.
The enantiomers can be used as pure D or I compound or as a mixture.
In one case, enantiomers can be separated by chiral chromatographic columns.
The enantiomers can be bases in which case the co-crystallization agents typically will be acids.
For example, the enantiomers can be resolved from the racemate using chiral chromatography or recrystallization.
The enantiomers can be prepared from the chiral precursors of the compound of formula ( III ).
The single enantiomers can be obtained in a crystalline form using the following procedure.
The single enantiomers can be separated from these mixtures by methods known in literature.
The separated enantiomers can be isolable and stable under appropriate storage and handling conditions.
These enantiomers can be used to make dimers per the above procedures, mutatis mutandis.
Pure enantiomers can be resolved from the pairs of enantiomers and the mixtures thereof ( racemates ).
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They may therefore exist as enantiomers or diastereoisomers
And enantiomers are just the mirror images
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