Examples of 'enol' in a sentence
Meaning of "enol"
enol (noun) - a term used in organic chemistry to describe a type of compound that contains a hydroxyl group attached to a double-bonded carbon atom
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- An organic compound containing a hydroxyl group bonded to a carbon atom which is doubly bonded to another carbon atom.
How to use "enol" in a sentence
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enol
An enol ether is an alkene with an alkoxy substituent.
The formation of an enol is catalyzed by acid or base.
Enol forms and tautomers are also included.
The expected enol ether was then distilled.
Enol and tautomeric forms are also included.
Tautomers include enol and keto forms.
Aryl enol phosphates formed in good yields ca.
The structure of a typical enol ether group.
The enol form is a vinylogous analogue of a carboxylic acid.
The compound is isolated as its enol ether.
Enol ethers are examples of such olefins.
Preparation of the silyl enol ether.
The enol sulfonate formation reaction is well known.
Ppm singlet originating from the enol proton.
The keto and enol tautomers of acetylacetone coexist in solution.
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The proton of the hydroxyl of the enol is removed.
Phenol therefore exists essentially entirely in the enol form.
The title compound is isolated as a mixture of enol ethers.
The diethyl enol phosphate gave the highest stereoselectivity.
Another way to look at ascorbic acid is to consider it as an enol.
Enol forms are also included.
Hydrolysis of the enol acetate.
Enol forms are also induded.
I is an anion of an organic acid or of an enol.
No enol ether precursor was detected.
Said replacement can be vÃa steroidal enol triflate or a halo derivative.
The silyl enol ether was used without further purification.
This ketone will prefer to exist in its enol tautomer in solution.
This enol ester is an activator.
It can spontaneously through equilibrium get to the actual enol form.
The preferred enol ether is the methyl or ethyl ether.
It is a type of enol.
The enol and keto forms are said to be tautomers of each other.
Silyl enol ether.
The enol intramolecular bond is disrupted by the solvents water and methanol.
Silyl enol ethers.
Enol ethers may be prepared using other methods known to the chemist.
This is an enol reaction.
The preferred enol ester forming trifluoromethanesulphonic acid derivative is trifluoroethanesulfonic anhydride.
It is also used for preparation of enol ethers and related functional groups.
The enol ether side product in the crude solid was hydrolysed as follows.
But in other instances the enol form can be present in higher concentration.
When the reactions are allowed to proceed at higher temperature enol lactones are formed.
Keto enol tautomery.
It was known that this reagent could chlorinate an enol and reduce a sulfoxide.
Reactions of silyl enol ethers with carbonyl compounds activated by titanium tetrachloride.
Preparations of several halogenated compounds including pharmaceutically interesting enol lactones are reported.
Catalytic amination of silyl enol ethers with azo diester compounds was investigated.
Heck reactions can also be performed smoothly on the enol triflate intermediate.
The enol substrate has very low solubility in most common solvents.
