Examples of 'chiral compounds' in a sentence
Meaning of "chiral compounds"
chiral compounds - This phrase is used in chemistry to refer to molecules that are non-superimposable mirror images of each other. Chiral compounds have different spatial arrangements of atoms
How to use "chiral compounds" in a sentence
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chiral compounds
It is used only when chiral compounds are being analyzed.
Chiral compounds are not mentioned at all.
Substituted binaphthyl derivatives are chiral compounds.
Many of the chiral compounds of this type are amines.
The active ingredients may also be chiral compounds.
Chiral compounds are ubiquitous in nature.
Leukotriene antagonists are chiral compounds.
Therefore chiral compounds are also encompassed by the present invention.
Of particular importance is the potential to reduce waste when resolving chiral compounds.
Chiral compounds can be employed as racemic mixtures or as pure enantiomers.
This invention relates to cycloalkanediols and their use in preparing chiral compounds.
Chiral compounds have the ability to rotate plane polarized light.
There is a large need to find a suitable enzyme for the preparation of these chiral compounds.
The numerals of the chiral compounds refer to the numerals indicated in the text.
The monomer unit VI and its precursor X are chiral compounds.
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All chiral compounds in the tables and schemes are racemic unless specified otherwise.
The compounds of formula 1 are chiral compounds.
The chiral compounds are comprised of carbon atom at center attached to four different substitutes.
The acid-labile proton pump inhibitors are chiral compounds.
Racemic mixtures of chiral compounds of formula I can be separated using chiral HPLC.
So, the same is very useful for the intermediates of other chiral compounds.
Preferred are chiral compounds of formula I.
Crystallization of the diastereomeric salts affords the acid salt of chiral compounds of formula 70.
In addition, both chiral compounds and racemic mixtures are encompassed by the present invention.
Not surprisingly, the enantiomers of such chiral compounds have different activities.
Many biologically active systems, however, involve specific enantiomers or diastereoisomers of chiral compounds.
My work also focuses on chiral compounds and the physical / chemical properties of organochlorine pesticides.
Additionally, such ligands can be used to prepare chiral compounds of high optical purity.
Chiral compounds of formula ( D ) can also be prepared following a similar procedure.
Thus, the catalyst of the invention may be used advantageously to prepare chiral compounds.
The chiral compounds contain at least one N-containing heterocyclic ring.
In addition, chiral intermediate compounds may be resolved and used to prepare chiral compounds.
Chiral compounds of formula ( I ) may also be obtained by enantioselective synthesis through chiral precursors.
Therefore, this method also has a fatal drawback for mass-production of chiral compounds.
Roughly 10 % of racemic chiral compounds crystallize as conglomerates.
Furthermore, chiral intermediates may be resolved and used to prepare chiral compounds of the invention.
These chiral compounds are obtained according to reaction schemes 2-4.
However, only very few esterases suitable for preparing chiral compounds are commercially available.
Chiral compounds according to formula II can e.g. be obtained as follows,.
However, this route has significant disadvantages, especially if one wishes to obtain chiral compounds.
Compound 225 illustrates that chiral compounds can be used to increase potency and selectivity.
This reaction sequence can be applied to achiral, racemic or chiral compounds of formula IC.
The compounds of the formula I are chiral compounds having chiral centers in positions 4a and 10b.
Reaction of a compound of formula 78 with a hydrazine generates chiral compounds of formula 79.
Chiral compounds are purified using Isopropanol / Hexane gradient, AD column.
The salts were the first synthetic non-carbon-containing chiral compounds.
The compounds of formula I are chiral compounds having chiral centers at least in positions 2, 4a and 10b.
The method of claim 15, wherein said chemical library comprises chiral compounds.
The present invention also further comprises chiral compounds of the formula ( XVII ) or ( XVIII ) wherein,.
However, the rate of success in obtaining such crystals is only 20 % with non chiral compounds.
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Examples of using Chiral
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An object that is not chiral is said to be achiral
Such chiral diols are important in organic synthesis
Many electrophiles are chiral and optically stable
Examples of using Compounds
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These compounds are not effective against spores
Delete volatile organic compounds content of products
These compounds are now under further investigation
