Examples of 'single enantiomer' in a sentence
Meaning of "single enantiomer"
Single enantiomer: A single enantiomer refers to a molecule that exists in only one chiral form, meaning it does not have a mirror image. This term is commonly used in the context of chemistry and drug development
How to use "single enantiomer" in a sentence
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single enantiomer
Wherein the chiral ligand is a single enantiomer.
Chiral drugs of single enantiomer have been widely used.
The product was isolated as a single enantiomer.
A sample with only a single enantiomer is an enantiomerically pure or enantiopure compound.
The product was islated as a single enantiomer.
The HCl salt of the single enantiomer remained as the thermodynamically stable anhydrous form.
The ligand of the present invention is a single enantiomer.
Some compounds have been obtained as a single enantiomer without knowing their absolute configuration.
This method is believed to be stereoselective if the reactant is a single enantiomer.
It is often desired to obtain a single enantiomer of a racemic lactam ester.
Fractional crystallization is another technique which may be employed to isolate a single enantiomer.
Other approaches involve optical resolution of a single enantiomer or diastereomer from a mixture.
This occurs when the racemic compound has relatively high solubility compared to the single enantiomer.
For any of the above compounds use of a single enantiomer is preferred herein.
A single enantiomer was observed by chiral HPLC analysis.
See also
Duloxetine is administered as a single enantiomer.
This salt was a single enantiomer by chiral HPLC.
The phosphorus ligands are preferably used in their single enantiomer form.
The product was a single enantiomer by chiral HPLC.
Preferably it is resolved by crystallisation in the presence of a single enantiomer of a chiral acid.
This salt was a single enantiomer by chiral CE.
It is preferred that a compound of the present invention exists as a single enantiomer or diastereomer.
Enantiomer A or enantiomer B refer to a single enantiomer whose absolute stereochemistry was not characterised.
This method can be carried out for both the racemate or a single enantiomer.
Typically, only a single enantiomer is pharmacologically active.
Debenzylating said enantiomer and recovering a single enantiomer of albuterol.
The single enantiomer emtricitabine has the structure,.
The procedure can be carried out for both the racemate or a single enantiomer.
Adding one equivalent of a single enantiomer of mandelic acid ;.
This chemistry can be carried out for both the racemate or a single enantiomer.
They may be in the form of a single enantiomer or diastereomer, or a racemate.
Determine optical purity by chiral SFC to show a single enantiomer.
Thus, synthetic routes to single enantiomer lipoic acid have been sought.
HPLC confirmed that this product consisted of a single enantiomer.
Thus, it may be preferable to use a single enantiomer for therapeutic applications.
Compounds as claimed in any of claims 1 to 5 which consist of a single enantiomer.
Optically pure compound - a single enantiomer which rotates plane polarized light.
Lactones of type 3 can be prepared in single enantiomer form.
A sample with only a single enantiomer is an enantiomerically pure, enantiopure or homochiral compound.
In this case cyclization of compound V will give a single enantiomer of formula II.
A method for obtaining a single enantiomer useful as a precursor for albuterol, comprising,.
In other embodiments, the compound is a pure single enantiomer.
Liberating said single enantiomer from said salt by treatment with a base ;.
A topical composition comprising substantially single enantiomer l-threo - methylphenidate.
The single enantiomer compounds of the present invention provide a cool / refreshing feeling.
A compound of any preceding claim, in the form of a single enantiomer or diastereomer.
If the case, either as a single enantiomer or mixture thereof and its pharmaceutically acceptable salts.
Formoterol and ritodrine may be racemic, or may be a substantially single enantiomer.
The process of the invention for preparing a single enantiomer of cyclohexylphenyl glycolic acid comprises,.
Consequently, there is a need for a process to produce that single enantiomer.
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Purification of the crude enantiomer crystals is easy
Simple deprotonation affords the pure enantiomer
Differences in enantiomer potency were also observed in vivo
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