Examples of 'diels-alder reaction' in a sentence
Meaning of "diels-alder reaction"
The Diels-Alder reaction is a chemical reaction that involves the formation of a new ring structure with the simultaneous creation of multiple bonds. It is a versatile and widely used transformation in organic chemistry, allowing the synthesis of complex compounds and the construction of intricate molecular architectures
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- The cycloaddition reaction between a conjugated diene and an alkene to form a cyclohexene ring.
How to use "diels-alder reaction" in a sentence
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diels-alder reaction
The Diels-Alder reaction is a pericyclic reaction.
This is an example of a hexadehydro Diels-Alder reaction.
They undergo Diels-Alder reaction with dienes.
Maleic anhydride is a dienophile in the Diels-Alder reaction.
The Diels-Alder reaction is performed in an organic solvent.
The cycloaddition may be a Diels-Alder reaction.
The retro Diels-Alder reaction is used in the industrial production of cyclopentadiene.
Naphthoquinone acts as strong dienophile in Diels-Alder reaction.
It is prepared by the Diels-Alder reaction of butadiene and cyclopentadiene.
Synthesis of glutaraldehyde via the Diels-Alder reaction.
Norbornene is made by a Diels-Alder reaction of cyclopentadiene and ethylene.
They are commonly employed as dienophiles in the Diels-Alder reaction.
Norbornadiene can be formed by a Diels-Alder reaction between cyclopentadiene and acetylene.
Unsaturated aldehydes can be prepared by the Diels-Alder reaction.
The Diels-Alder reaction between a dienophile 6 and cyclopentadiene was therefore studied.
See also
The most important of these is the Diels-Alder reaction.
The Diels-Alder reaction is an additive reaction of an olefin with a conjugated diene.
An important reaction for conjugated dienes is the Diels-Alder reaction.
This liquid is used as a catalyst in a Diels-Alder reaction of cyclopentadiene with methyl acrylate.
Chlorendic acid is industrially produced in high volumes by Diels-Alder reaction.
The Diels-Alder reaction may be performed in the absence or in the presence of a solvent.
Himbacine has been synthesized using a Diels-Alder reaction as a key step.
The Diels-Alder reaction of cyclopentadiene with furan can produce two isomeric products.
The solution is used directly in the following Diels-Alder reaction.
The concerted mechanism of the Diels-Alder reaction between benzyne and furan is shown below.
These compounds can be prepared by utilizing the Diels-Alder reaction.
The Diels-Alder reaction is perhaps the most important and commonly taught cycloaddition reaction.
It is not necessary to use a catalyst to advance the Diels-Alder reaction.
The Diels-Alder reaction may be carried out under conventional conditions known in the art.
In the first step, hexachlorocyclopentadiene reacts with cyclopentadiene in a Diels-Alder reaction.
The conjugated isoprenoid and a dienophile in a Diels-Alder reaction may each demonstrate stereoisomerism.
The reaction that these compounds undergo is typically referred to as a Diels-Alder reaction.
This prediction agrees with experiment as the Diels-Alder reaction is a rather facile pericyclic reaction.
In the first step the triazine reacts with the fullerene in a Diels-Alder reaction.
The same solvent is used in both the Diels-Alder reaction and in the hydrogenation reaction.
The radical initiator is not needed when the crosslinking is performed by a Diels-Alder reaction.
This reaction is a derivative of the established Diels-Alder reaction and proceeds via a similar cycloaddition mechanism.
This content is indirectly measured by chemical methods that employ the Diels-Alder reaction.
The dienophile undergoes Diels-Alder reaction with a diene introducing such a functionality onto the product molecule.
In a first study, a modification method based on the Diels-Alder reaction is developed.
Retro Diels-Alder reaction.
Aldrin is produced by combining hexachlorocyclopentadiene with norbornadiene in a Diels-Alder reaction to give the adduct.
Asymmetric Diels-Alder reaction.
The reactivity of such alkynes according to inverse electron demand Diels-Alder reaction was explored.
In certain embodiments, the Diels-Alder reaction is performed in a solvent.
This property makes them reactive substrates in certain organic reactions such as the Diels-Alder reaction.
The stereochemistry of the adducts obtained in the Diels-Alder reaction has been determined by 1H nmr.
One example of the Diels-Alder reaction of 2-carboxylated diethyl vinylphosphonates is reported.
The limits of reactivity of this diene in the Diels-Alder reaction have been highlighted.
The preferred Diels-Alder reaction is the inverse-electron demand Diels-Alder cycloaddition.
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Examples of using Diels-alder
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The Diels-Alder reaction is a pericyclic reaction
This is an example of a hexadehydro Diels-Alder reaction
They undergo Diels-Alder reaction with dienes
