Examples of 'tautomerism' in a sentence
Meaning of "tautomerism"
tautomerism (noun) - this term is used in organic chemistry to describe the phenomenon where a compound exists in two or more isomeric forms that can readily interconvert by a chemical reaction called tautomerization. These isomers, known as tautomers, have the same molecular formula but differ in the position of protons and double bonds
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- A form of isomerism in which a dynamic equilibrium between multiple isomers exists, such as that between an enol and a ketone.
How to use "tautomerism" in a sentence
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tautomerism
Tautomerism may also result in aromatic structures.
Compounds of the present invention exhibit tautomerism.
Similar tautomerism is observed for corresponding heterocyclic compounds.
The concept of tautomerizations is called tautomerism.
Tautomerism involves a base being changed by the repositioning of a hydrogen atom.
The compounds of the invention may exhibit tautomerism.
The moiety exhibits the tautomerism represented by the equation of.
The compounds may exhibit tautomerism.
Tautomerism is possible in the herbicide carbocyclic or heterocyclic compounds of this invention.
Certain compounds may exhibit tautomerism.
This lactam lactim tautomerism can also be exhibited in many related compounds.
The compound of the invention may exhibit tautomerism.
Similar tautomerism may be found with compounds containing certain heterocyclic groups.
The present compounds exhibit tautomerism.
Tautomerism is a sort of dynamic isomerism shown by certain unstable molecules which change in structure.
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The compound exhibits tautomerism.
Another example of tautomerisms is phenol-keto tautomerism.
The concept of tautomers that are interconvertable by tautomerizations is called tautomerism.
An example of ketone-enol tautomerism are as shown below.
Compounds disclosed herein may exhibit the phenomenon of tautomerism.
Keto-enol tautomerism is catalyzed by either acid or base.
Nomenclature and tautomerism.
Keto-enol tautomerism equilibrium of acetone.
The compounds of the invention may exhibit the phenomenon of tautomerism.
Keto - enol tautomerism is catalyzed by either acid or base.
The broadening is attributed to chemical shift exchange due to the tautomerism.
Keto - enol tautomerism is important in several areas of biochemistry.
It is to be understood that compounds disclosed herein may exhibit the phenomenon of tautomerism.
This tautomerism may be depicted as follows,.
Certain reagents and products disclosed in this application may exhibit tautomerism.
Prototropic tautomerism may be considered a subset of acid-base behavior.
The chemical formulae referred to herein may exhibit the phenomenon of tautomerism.
Of the various types of tautomerism that are possible, two are commonly observed.
Papers on the subject of ring tension and double bonds as well as valency tautomerism.
The tautomerism is proposed to occur through a hydrogen-bonded cyclic dimer.
The compound of the present invention may exhibit tautomerism or structural isomerism.
The reaction which includes simple proton transfer in an intramolecular manner is called a tautomerism.
Notably, amycolamicin has tautomerism and thus encompasses tautomers thereof.
The chemical formulae referred to herein may exhibit the phenomena of tautomerism or conformational isomerism.
In keto-enol tautomerism a simultaneous shift of electrons and a hydrogen atom occurs.
The inventive compounds herein may exhibit the phenomena of tautomerism and structural isomerism.
In addition, isomers due to tautomerism are all encompassed by the present invention, too.
The chemical formulae referred herein may exhibit the phenomena of tautomerism or structural isomerism.
The enamine-imine tautomerism may be considered analogous to the keto-enol tautomerism.
The compounds disclosed herein and covered by the above formulae may exhibit tautomerism.
These compounds are in keto-enol tautomerism so that they may interconvert to each other.
Tautomers It is understood that some compounds may exhibit tautomerism.
Tautomerism of Compound 1 NMR studies were performed to analyze the tautomers of Compound 1.
The chemical formulae referred to herein may exhibit the phenomena of tautomerism and structural isomerism.
A non-limiting example of tautomerism in is shown below as tautomer A and tautomer B.
