Examples of 'pure enantiomers' in a sentence
Meaning of "pure enantiomers"
pure enantiomers: Refers to a set of molecular compounds that are mirror images of each other but cannot be superimposed, often used in chemistry and pharmacology contexts
How to use "pure enantiomers" in a sentence
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pure enantiomers
Pure enantiomers may also be synthesized directly.
Also included are the essentially pure enantiomers.
The two pure enantiomers are recovered in a following stage.
Especially preferred are the pure enantiomers.
The pure enantiomers possess higher inhibitory activities.
Yielding the two title compounds as pure enantiomers.
Optically pure enantiomers of mandelic acid are commercially available.
Four more recrystallizations yielded the respective pure enantiomers.
The pure enantiomers allow an optically active polymer to be prepared.
Racemates obtained can be separated into the pure enantiomers.
The two pure enantiomers of the diphosphine are recovered by carrying out the decomplexation.
These compounds may exist as mixtures of enantiomers or as pure enantiomers.
Optically pure enantiomers of irinotecan can be prepared by methods well known in the art.
Hydrolyzing the individual diastereomers to the corresponding pure enantiomers.
Optically pure enantiomers of didesmethylsibutramine can be prepared using techniques known in the art.
See also
This invention pertains to racemic mixtures and to pure enantiomers.
This invention provides both the pure enantiomers or diasteromers and mixtures thereof.
Chiral compounds can be employed as racemic mixtures or as pure enantiomers.
This invention claims the pure enantiomers and diastereomers as well as the mixtures.
An optically active polymer can be prepared using the pure enantiomers.
To obtain pure enantiomers chiral chromatography is a promising technique which produces high purity enantiomers.
The racemate was subjected to chiral separation so to obtain the pure enantiomers.
The racemates and the pure enantiomers of these compounds also form part of this invention.
As their racemates or in enantiomerically enriched form preferably the pure enantiomers.
It will be appreciated that pure diastereomers and pure enantiomers represent preferred embodiments.
None of these documents refer to any enantiomerically enriched compounds or pure enantiomers.
Both the pure enantiomers and racemic mixtures are within the scope of the present invention.
Optically active compounds can be employed as racemic mixtures or as pure enantiomers.
The pure enantiomers La and Ib be obtained by chiral separation using a chiral column.
A process by which a racemic mixture is separated into its two pure enantiomers.
The pure enantiomers La and Ib may be obtained by chiral separation using chiral columns.
Neither crystalline lactic acid esters nor pure enantiomers thereof are described.
Preferably chiral long acting anticholinergics are present in form of one of their pure enantiomers.
The same applies for the pure enantiomers of formula I and salts thereof.
Diastereomer crystallization is widely used for the industrial synthesis of pure enantiomers.
As pure enantiomers or stereoisomers as well as mixtures of different isomers such as e . g.
The diastereomers may then be separated in order to recover the optically pure enantiomers.
Accordingly, the pure enantiomers and the salts thereof are also part of the invention.
In this case a separate enzyme system can be employed to produce optically pure enantiomers.
Pure enantiomers can be resolved from the pairs of enantiomers and the mixtures thereof ( racemates ).
Eluted with ethanol in heptane and concentrated the fractions to provide pure enantiomers.
When optically pure enantiomers are used, those in S-configuration are preferred.
The auxiliary group can then be cleaved to provide the desired pure enantiomers.
They may therefore be in the form of pure enantiomers or of their mixtures . STR3.
These melting points are often lower than those of the corresponding pure enantiomers.
To produce pure enantiomers of compounds of Formula I where R3 is hydroxy, Scheme 5 may be used.
Compounds with stated absolute stereochemistry were obtained as pure enantiomers of the depicted structure.
Thus, optically pure enantiomers of 100 % purity can be obtained under the described conditions.
Numerous methods exist for separating a racemic mixture into its two pure enantiomers.
Compound 4 was separated into the pure enantiomers 4a, and 4b by using a chiral column.
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Examples of using Enantiomers
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Not all enantiomers have distinguishable odors
They may therefore exist as enantiomers or diastereoisomers
And enantiomers are just the mirror images
Examples of using Pure
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Pure distilled water or softened water is being used
Quality clothing of pure camel hair in mongolia
Pure commercial relationships are often not possible
