Examples of 'stereochemical' in a sentence
Meaning of "stereochemical"
Stereochemical relates to the spatial arrangement of atoms in molecules and the effects of this arrangement on the chemical properties of the compound. It is used in chemistry to describe the three-dimensional structure and characteristics of molecules
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- Of or pertaining to stereochemistry
How to use "stereochemical" in a sentence
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stereochemical
Stereochemical exchange that causes sterochemical inversion.
Ladderanes have two types of stereochemical relationships.
All known stereochemical details should be provided.
This arrangement leads to three stereochemical outcomes.
Stereochemical studies indicate that acetoxypalladation is nonstereospecific.
Formoterol can exist in four stereochemical forms.
Stereochemical strain due to polar repulsive forces.
Numerous chemical targets have distinct stereochemical demands.
The stereochemical consequences of electron delocalization in extended π systems.
The relation of a chemical reaction to stereochemical substituent constants.
The stereochemical control is seriously limited.
Be sure to include the stereochemical outcome.
The stereochemical course of the tremulane biosynthesis is discussed.
The synthesis uses a route maintaining stereochemical integrity.
The stereochemical control is very high.
See also
Some compounds also form trans stereochemical isomers.
Stereochemical configurations depicted at asterisk positions indicate absolute stereochemistry.
Polypropylene may vary by stereochemical structure.
The stereochemical forms can be separated or isolated by standard procedures.
Those acyltransferases regulate fatty acid stereochemical distribution.
The stereochemical mixture of d is resolved into peaks containing e and h.
The compounds can hence exist in various stereochemical forms.
Stereochemical isomers are intended to be included within these compound definitions.
This mechanism is in accord with the following stereochemical results.
A stereochemical comparison with trifluoperazine suggests similar calmodulin binding mechanisms.
Analysis of this data led to structural and stereochemical assignments.
The stereochemical outcome is compared with similar reactions in organic solvents.
Or a pharmaceutical acceptable addition salt or a stereochemical isomeric form thereof.
Proper stereochemical outcome may be dependent on the quantity of catalyst employed.
Straight bonds are intended to include all possible stereochemical configurations.
It resolves a key stereochemical difficulty by incorporating a carefully designed synthetic pathway.
The compounds provided herein may encompass various stereochemical forms.
This results in a plethora of stereochemical configurational and conformational structural possibilities.
The compounds of the invention can exist in various stereochemical forms.
A preferred stereochemical configuration around the cyclopropyl ring of phenylcyclopropylamine is trans.
Configurational correlations will elucidate the stereochemical course of uricolytic transformations in vivo.
Here the stereochemical outcome is determined by relaxation of the excited double bond.
The length of the tether affects the stereochemical outcome of the reaction.
A variety of stereochemical and selectivity data suggest that this is an ionic addition.
The data provide information about the stereochemical effects of base methylation.
Kinetic and stereochemical evidence is presented in support of the proposed reaction pathways.
Epimers are diastereomers that differ in stereochemical configuration at only one chiral center.
Proper stereochemical outcome has been found to be dependent on the quantity of catalyst employed.
There are also conformational and stereochemical effects specific to the pyranose ring.
Proper stereochemical outcome has been shown to be dependent on the quantity of catalyst employed.
Other analytical methods for demonstrating stereochemical homogeneity are known in the field.
Subsequent stereochemical studies indicated that both pathways occur and are dependent on chloride concentrations.
The process results in the production of a stereochemical isomer of a dioxolane nucleoside analogue.
Studies on the oxidation of unsaturated carbonyl compounds also provide stereochemical insight.
The invention contemplates all stereochemical forms of the compounds provided herein.
