Examples of 'relative stereochemistry' in a sentence
Meaning of "relative stereochemistry"
relative stereochemistry: In chemistry, this term refers to the arrangement of atoms in space within molecules and their relationship to one another
How to use "relative stereochemistry" in a sentence
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relative stereochemistry
In this manner relative stereochemistry is conveyed unambiguously.
The solid and dotted wedges are also used to indicate relative stereochemistry.
The stereochemistry listed is relative stereochemistry unless otherwise noted.
Relative stereochemistry was not assigned.
Racemic compounds possessing such indicated relative stereochemistry are marked with.
The relative stereochemistry has been confirmed by NOE experiments unequivocally.
The stereochemistry indicated in compound XII is intended to reflect relative stereochemistry only.
The descriptors only describe relative stereochemistry rather than absolute stereochemistry.
Relative stereochemistry can be deduced from nOe 's and interproton coupling.
It is important mention that the relative stereochemistry was unambiguous determined by x-ray crystallography.
The use of a chiral auxiliary may assist control of absolute and / or relative stereochemistry.
Rearrangements where the relative stereochemistry of the ligand change within the coordination sphere.
R / S stereochemical assignments have been used to define the relative stereochemistry of molecules.
The relative stereochemistry at Se alternates along the polymer chain syndiotactic.
The compounds of the present invention have the relative stereochemistry shown in structure ( I ).
See also
The indicated relative stereochemistry was assigned on the basis of NOE studies.
A compound according to claim 1 wherein the R4a and R10a substituents have a trans relative stereochemistry.
The relative stereochemistry of the pyrimidine side chain was confirmed via nuclear Overhauser enhancement study.
Compounds designated ( R / S ) are racemic compounds where the relative stereochemistry is as drawn.
Cis / trans relative stereochemistry was assigned based on NMR.
This material is a single diastereomer ( > 6:1 diastereomeric ratio but unconfirmed relative stereochemistry at the aminal center ).
Assignment of relative stereochemistry was made by X-ray crystallographic structure determination.
The separation, 1H n . m . r . spectroscopy, and relative stereochemistry of the diastereoisomers are discussed.
The relative stereochemistry of these compounds was assessed vÃa NMR studies and / or X-ray diffraction.
Formula ( I ) shows the relative stereochemistry of the chiral centres.
Relative stereochemistry was assigned based on 1H NMR and NOE studies.
Both the ratio and relative stereochemistry was demonstrated through X-ray analysis.
The relative stereochemistry of the two diastereomers of EXAMPLE 1 is shown in the figure below.
Dia 1 and Dia 2 display a trans relative stereochemistry, Dia 3 and Dia 4 display a cis relative stereochemistry.
The relative stereochemistry of the major isomer was determined to be cis by 2D NMR.
Therefore, the relative stereochemistry of the H10 and H11 protons in compound 7 had to be cis.
The relative stereochemistry was determined using Nuclear Overhauser Effect ( NOE ) experiment.
The relative stereochemistry of the products has been established by analysis of 1H and 13C NMR spectra.
The relative stereochemistry that is obtained is shown in formulae ( XI ) and ( XII ).
The relative stereochemistry anti has been determined by dipolar correlations between CH ( 9 ) and CH2 ( 5 ) ax.
The relative stereochemistry of the substituents on C-1 and C-9 is determined as cis by NOE-experiments.
The relative stereochemistry of the substituents on C-1 and C-9 is determined as trans by NOE-experiments.
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Examples of using Stereochemistry
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Indicate whether the stereochemistry is absolute or relative
He is best known for his work in stereochemistry
The stereochemistry of this transport model is discussed
