Examples of 'cycloaddition' in a sentence
Meaning of "cycloaddition"
cycloaddition (noun): Cycloaddition is a chemical process in which two or more molecules combine to form a cyclic compound. This reaction typically involves the formation of new carbon-carbon bonds and the creation of a ring structure. Cycloaddition reactions are important in organic chemistry and are used to synthesize complex molecules and functionalize compounds
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- An addition reaction that leads to the formation of a cyclic product.
How to use "cycloaddition" in a sentence
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cycloaddition
The reaction is thought to proceed via cycloaddition.
Benzynes undergo cycloaddition with a wide range of olefins.
An example of this type of reaction is a cycloaddition reaction.
Cycloaddition is usually assisted by light or heat.
Many methods rely on cycloaddition reactions.
Cycloaddition of a nitrone to an unsaturated group or double bond of the polysisoprene.
The final step is a photolytic cycloaddition.
Trimethylenemethane cycloaddition which can proceed via a similar mechanism.
Photolysis leads to dimerization via a cycloaddition.
Microwave activation of the cycloaddition reaction proved to be very efficient.
The reaction between norbornadiene and an activated alkyne is a cycloaddition.
Dipolar cycloaddition with azides.
Norbornadiene is reactive in cycloaddition reactions.
Indolyne undergoes cycloaddition with cyclopentadiene to afford complex tetracyclic product.
The first part is a cycloaddition.
See also
Other photochemical cycloaddition reactions with alkenes occur through excimers.
Azide alkyne huisgen cycloaddition.
Cycloaddition of a nitrile imine to an unsaturated group or double bond of the polysisoprene.
Examples of all three modes of cycloaddition are discussed in this section.
Cycloaddition of a nitrile oxide to an unsaturated group or double bond of the nolvsisonrene.
The ketene and imine upon cycloaddition provide the azetidinone.
The cycloaddition of cyclopentenone to all the halogenated ethylenes has been studied.
These oximes was converted to nitrile oxides by cycloaddition to provided these heterocycles.
The cycloaddition reaction is generally complete after about two hours.
It is also used as a nitrene source and as a substrate for cycloaddition reactions.
Further cycloaddition reactions.
The triple bond easily undergoes both and cycloaddition reactions.
Alternatively the known cycloaddition reaction to a suitably protected piperidinone can be applied.
Considering the cycloaddition.
Cycloaddition reactions can be used to form the fibers of the present disclosure.
Cu is not the only metal capable of catalyzing this type of cycloaddition.
The mechanism of the cycloaddition reaction and the stereochemical assignments are also discussed.
Preferred types of pericyclic reactions include but are not limited to cycloaddition reactions.
Cycloaddition with acrylates requires additional oxidation of the intermediate pyrazoline to the pyrazole.
The quadricyclane ligation utilizes a highly strained quadricyclane to undergo cycloaddition with π systems.
Cycloaddition with an acrylate requires additional oxidation of the intermediate pyrazoline to the pyrazole.
It was observed that fluoride substitution has an accelerating effect on the cycloaddition with azide.
The reaction kinetics for cycloaddition with the prototypical azide benzyl azide were investigated.
Suitable such catalysts are known in the art for use in click cycloaddition reactions.
The results obtained indicate that the cycloaddition is a concerted process with a high degree of synchrony.
Coupling the first switch intermediate to the second switch intermediate may comprise a cycloaddition reaction.
The one or more cycloadditions may comprise a Huisgen cycloaddition.
The second switch intermediate may be attached to the first switch intermediate through a cycloaddition reaction.
A preferred type of cycloaddition reaction according to one embodiment of the invention is a Huisgen cyclization.
The first and second guest molecules may be Capable or participating in a cycloaddition reaction.
This cycloaddition reaction takes place under pressure and heating conditions according to known methods S.
The nitrones are used directly in the cycloaddition reactions described in scheme A.
Cycloaddition reactions of the compound of general formula XXX with maleimide Fig.
One example is a palladium-catalyzed cycloaddition of trimethylenemethane.
Cycloaddition in Water.
