Examples of 'stereoselective' in a sentence

Meaning of "stereoselective"

stereoselective (adjective) - In chemistry, stereoselective refers to a reaction or process that produces a specific stereoisomer in preference to others
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  • Of a chemical reaction in which the production of one stereoisomer is favoured over all others.

How to use "stereoselective" in a sentence

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stereoselective
Stereoselective fluorinations may be either diastereoselective or enantioselective.
The pharmacokinetics of zopiclone in humans are stereoselective.
Stereoselective synthesis allows one form to predominate.
That document does not teach a stereoselective method.
Stereoselective process and crystalline forms of a camptothecin.
Such techniques are referred to as stereoselective synthesis.
Process for the stereoselective transformation of a diol to an alcohol.
The reaction is regioselective and stereoselective.
Stereoselective synthesis of phosphorus containing actives.
Chlorine or iodobenzene dichloride effected moderately stereoselective chlorodestannylation.
The conditions for stereoselective reduction of pyridine derivatives are described.
And therefore not to be very stereoselective.
This method is believed to be stereoselective if the reactant is a single enantiomer.
Stereoselective protonation of an enolate ion.
There are two important criteria in stereoselective alkylation of amines.

See also

Stereoselective hydrogenation of an enone double bond present in a steroidal compound is described.
This characteristic avoids a stereoselective synthesis of the anomeric center.
The peptide structure allows an intramolecular and stereoselective reaction.
This allows for the stereoselective synthesis of cyclic phosphites.
Its metabolism is highly stereoselective.
Method for the stereoselective preparation of amino acid derivatives.
The enantiomers can be prepared through stereoselective synthetic process.
Therefore a general stereoselective synthesis of cis nucleoside analogues is an important goal.
Such techniques include but are not limited to stereoselective dihydroxylation.
Agonist stimulation was stereoselective and was blocked by addition of a specific antagonist.
This results in a stronger nucleophile that initiates a stereoselective aldol reaction.
These results were confirmed by stereoselective synthesis of the enantiomers of tranylcypromine.
Glucuronidation in human liver microsomes like in rat liver microsomes is stereoselective.
Thus the selectivity of the stereoselective hydrogenation can be determined indirectly.
Example of an enantiomeric pair with different affinity for a stereoselective receptor.
Two exemplary stereoselective schemes will be discussed in the present disclosure.
Example of an enantiomeric pair with different affinities for a stereoselective receptor.
This allows for the stereoselective synthesis of cyclic phosphoramidites of prodrugs.
The direct insertion of magnesium into alkenyl halides is not stereoselective.
Peptidomimetic compounds may be prepared by stereoselective synthetic processes described herein.
Stereoselective reduction may be accomplished by use of chiral reagents known in the art.
Respective optical isomers can be prepared through stereoselective synthetic process.
Curran is also a pioneer in stereoselective radical reactions and radical translocation reactions.
These processes preferably employ watersoluble enzymes capable of catalyzing stereoselective hydrolysis.
It is therefore possible to do stereoselective synthesis using the method of the present invention.
Therefore it is a big challenge to perform the hydrogenation both in a stereoselective and chemoselective manner.
The stereoselective synthesis of the invention can be carried out at atmospheric pressure.
Reduction of alkynes is a useful method for the stereoselective synthesis of disubstituted alkenes.
The stereoselective binding to serum albumin of the two conformations has been reported to differ.
The novel method provides a commercially viable stereoselective synthesis of benzimidazole sulfoxides.
The stereoselective reduction of a substrate may occur with or without high yields of product.
Said intermediate is then subjected to a stereoselective resolution process to obtain the suitable enantiomer.
A stereoselective reaction can be carried out by selecting a reagent and a leaving group to be used.
This reference states that terfenadine does not undergo any stereoselective isomeric interconversion in man.
The stereoselective reaction should also be simple to perform and applicable on an industrial scale.

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