Examples of 'stereoselective synthesis' in a sentence
Meaning of "stereoselective synthesis"
stereoselective synthesis: In chemistry, this term describes a reaction that generates one stereoisomer in preference to others
How to use "stereoselective synthesis" in a sentence
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stereoselective synthesis
Stereoselective synthesis allows one form to predominate.
Such techniques are referred to as stereoselective synthesis.
Stereoselective synthesis of phosphorus containing actives.
This characteristic avoids a stereoselective synthesis of the anomeric center.
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.
A process for the stereoselective synthesis of the amines and their precursors could provide certain advantages.
The novel method provides a commercially viable stereoselective synthesis of benzimidazole sulfoxides.
The stereoselective synthesis of the alkylated oxindole 2a or 2b is an exothermic reaction.
The present invention relates to the enantiomeric enrichment and stereoselective synthesis of chiral amines.
This allows for the stereoselective synthesis of cyclic phosphites.
S-mirtazapine can also be obtained by stereoselective synthesis.
Therefore a general stereoselective synthesis of cis nucleoside analogues is an important goal.
The structural specificity and instability under a basic condition make the stereoselective synthesis of voriconazole difficult.
This allows for the stereoselective synthesis of cyclic phosphoramidites of prodrugs.
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Hence, transaminases are useful for the enantiomeric enrichment and stereoselective synthesis of chiral amines.
Scheme 2 presents a stereoselective synthesis of the linker portion of the macrocycle.
For example, cis / trans mixtures can be separated into the individual stereoisomers by stereoselective synthesis.
These results were confirmed by stereoselective synthesis of the enantiomers of tranylcypromine.
Stereoselective synthesis of vinyl iodide 24.
It is therefore possible to do stereoselective synthesis using the method of the present invention.
The invention described herein relates to a chemical process for the stereoselective synthesis of R - ( - ) - carnitine.
Thus, a stereoselective synthesis for preparation of these compounds would be highly desirable.
The present inventors have also devised a stereoselective synthesis route for the stereoisomers of interest.
Stereoselective synthesis of aldehyde 35.
The following shows a general reaction scheme for the stereoselective synthesis of various phenylcyclobutyl derivatives.
The stereoselective synthesis of the invention is carried out at a temperature of 5°C to 30°C.
The techniques for carrying out the stereoselective synthesis do not present any unusual difficulties.
Key words, renin, inhibitor, peptidomimetic, stereoselective synthesis.
A method for the stereoselective synthesis of the valnoctamide according to claim 9 wherein.
Preferably, the method that is used results in the stereoselective synthesis of a compound described herein.
A process for the stereoselective synthesis of physostigmine of the formula wherein the process comprises,.
The experimental section presents the development of a stereoselective synthesis to obtain 7'-hydroxylignanolactones.
A method for the stereoselective synthesis of the 2S stereoisomer of propylisopropyl acetamide comprising ;.
For examples of other organometallic reagents for the stereoselective synthesis of secondary alcohols from aldehydes,.
A method for the stereoselective synthesis of the 2R stereoisomer of propylisopropyl acetamide comprising ;.
The hydride reduction of the 4-carbonyl groups allows the stereoselective synthesis of substituted 2-hydroxy butyrolactones.
A method for stereoselective synthesis of an ( R ) - N - methylnaltrexone salt comprising,.
The present invention discloses a stereoselective synthesis of certain compounds of formula ( I ).
Therefore, a general stereoselective synthesis of biologically active B-nucleoside analogues is an important goal.
This stereospecificity can be exploited in a stereoselective synthesis of prodrug derivatives of Formula ( I ).
A process for stereoselective synthesis of a compound of Formula ( I ) wherein,.
The present invention discloses an efficient stereoselective synthesis of certain compounds of Formula ( I ).
The instant invention provides a stereoselective synthesis for the ring-substituted analogs of gabapentin.
This Example provides a concise, stereoselective synthesis of Compound 101.
An application is given with the stereoselective synthesis of a trisubstitued ethylenic? - diol with a Z configuration.
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Stereoselective fluorinations may be either diastereoselective or enantioselective
The pharmacokinetics of zopiclone in humans are stereoselective
Stereoselective synthesis allows one form to predominate
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Compilation and synthesis of fourth national communications
Two other documents complete this synthesis
Third synthesis report on activities implemented jointly
