Examples of 'asymmetric carbon atom' in a sentence
Meaning of "asymmetric carbon atom"
Phrase: asymmetric carbon atom. Definition: In organic chemistry, an asymmetric carbon atom, also known as a chiral center, is a carbon atom that is bonded to four different substituents. This results in the molecule having non-superimposable mirror images, which are referred to as enantiomers
How to use "asymmetric carbon atom" in a sentence
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asymmetric carbon atom
Prasugrel has an asymmetric carbon atom.
Asymmetric carbon atom.
Aclidinium is a quaternary ammonium cation with an asymmetric carbon atom.
An asymmetric carbon atom may exist also in a substituent such as alkyl group.
The lercanidipine molecule has one asymmetric carbon atom.
Ofloxacin has an asymmetric carbon atom at the 3-position and is obtained as a racemic mixture.
Stereoisomers are those compounds where there is an asymmetric carbon atom.
This compound has an asymmetric carbon atom and, therefore, the term phosphoglycerides includes stereoisomers.
The thiazole derivatives defined above have an asymmetric carbon atom.
The compound ( I ) has an asymmetric carbon atom and may therefore exist in two stereoisomeric forms.
The compounds of the invention may contain an asymmetric carbon atom.
The resulting asymmetric carbon atom at position 1 should preferably have an R configuration.
Some compounds of the invention contain an asymmetric carbon atom in their structure.
Glycine has no asymmetric carbon atom and is simply referred to as " Gly " or G.
The compounds of the present invention may have an asymmetric carbon atom.
See also
The substituent R4 at this asymmetric carbon atom is in a B-configuration for obtaining higher antimicrobial activity.
Certain compounds of this invention may have at least one asymmetric carbon atom.
The intermediate compound R - V bears the asymmetric carbon atom that imparts the optical activity to silodosin.
The compounds of the present invention contain one or more asymmetric carbon atom.
The compounds of Formula I contain an asymmetric carbon atom in the aliphatic ring moiety.
The compounds of the invention may also contain more than one asymmetric carbon atom.
Compound 7 having an asymmetric carbon atom denoted as " d " can have a specific stereoconfiguration.
The compounds of formula V contain an asymmetric carbon atom.
Finally, the malonyl asymmetric carbon atom may have either the R - or S-configuration.
The compounds of formula I have an asymmetric carbon atom.
Vedaprofen contains an asymmetric carbon atom and, therefore, is a racemic mixture of a ( + ) enantiomer and a ( - ) enantiomer.
The compounds of this invention may have an asymmetric carbon atom in their structure.
It is possible that compounds of Formula I may contain more than one asymmetric carbon atom.
Compounds of formula ( I ) contain an asymmetric carbon atom and have optical 1 and d isomers.
The compounds of the general formula I contain an asymmetric carbon atom.
The configuration at the asymmetric carbon atom can be R, S, or racemic.
In order to be chiral, a molecule should have an asymmetric carbon atom.
Formula ( La ) means that the asymmetric carbon atom C * is of the S configuration.
The compounds of Formula III contain an asymmetric carbon atom.
For example, R4 may comprise an asymmetric carbon atom when R4 is branched alkylene.
As is apparent from the structure of lactic acid, it has an asymmetric carbon atom.
The absolute configuration about the asymmetric carbon atom can be D or I.
In addition, the compound of the present invention has an asymmetric carbon atom.
Unless otherwise indicated, products comprising an asymmetric carbon atom were obtained in the racemic form.
In the compound of formula I, the nitrogen heterocycle of pyrrolidine structure comprises 1 asymmetric carbon atom.
They are racemates because of the asymmetric carbon atom at the 2-position.
Chiral 1,2-aminoalcohols are characterized by the presence of at least one asymmetric carbon atom.
According to the Cahn-Ingold-Prelog convention the asymmetric carbon atom can be of the " R " or " S " configuration.
With regard to stereoisomers, the compounds of structure ( I ) have more than one asymmetric carbon atom.
In the compound of formula I, the * indicates the asymmetric carbon atom in this compound.
Rotigotine, fentanyl oxybutynine and fesoterodine all contain one asymmetric carbon atom.
The compounds described above are characterized by the asymmetric carbon atom marked with an asterisk ( * ).
When R denotes hydrogen, the molecules of formula I contain a single asymmetric carbon atom.
The derivative according to claim 6, wherein the asymmetric carbon atom has the ( R ) configuration.
In addition, the amino acid or peptide residue may have an asymmetric carbon atom.
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