Examples of 'cycloaddition reaction' in a sentence
Meaning of "cycloaddition reaction"
cycloaddition reaction - A chemical reaction in which multiple unsaturated molecules combine to form a cyclic compound, often involving the breaking and formation of multiple bonds in the process
How to use "cycloaddition reaction" in a sentence
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cycloaddition reaction
An example of this type of reaction is a cycloaddition reaction.
The cycloaddition reaction is generally complete after about two hours.
Microwave activation of the cycloaddition reaction proved to be very efficient.
Coupling the first switch intermediate to the second switch intermediate may comprise a cycloaddition reaction.
Alternatively the known cycloaddition reaction to a suitably protected piperidinone can be applied.
The second switch intermediate may be attached to the first switch intermediate through a cycloaddition reaction.
The mechanism of the cycloaddition reaction and the stereochemical assignments are also discussed.
The first and second guest molecules may be Capable or participating in a cycloaddition reaction.
A preferred type of cycloaddition reaction according to one embodiment of the invention is a Huisgen cyclization.
For example, one particular approach for the cycloaddition reaction is shown below.
This cycloaddition reaction takes place under pressure and heating conditions according to known methods S.
In an advantageous embodiment, said cycloaddition reaction comprises the following steps,.
With these compounds, were prepared heterocycles azides derivatives as intermediates for the second cycloaddition reaction.
As specified above, the cycloaddition reaction is advantageously obtained without catalyst or other additives.
The Diels-Alder reaction is perhaps the most important and commonly taught cycloaddition reaction.
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New functionalisation strategies by azide-alkyne cycloaddition reaction at the periphery of aromatics cores, were developped.
FIGURE 3 provides a Table illustrating the effects of various solvents on the azide-haloalkyne cycloaddition reaction.
Another click chemistry reaction is the Diels-Alder cycloaddition reaction between a diene and a dienophile.
Apparently, the cycloaddition reaction of the LPP material predominates the thiolene addition.
Otto Diels and Kurt Alder discovered the Diels-Alder cycloaddition reaction for forming ring molecules.
Comprising the cycloaddition reaction in a non-polar solvent of a compound of formula ( II ),.
Figure 12 illustrates the cyclization of a linear peptide using the azide / alkyne cycloaddition reaction.
Alkyne 78 may be homologated and undergo a cycloaddition reaction to generate intermediate 79.
Other nitrile oxide reagents may be employed in the ( 2 + 3 ) cycloaddition reaction.
Diels-Alder cycloaddition reaction.
Contacting the product of step ( b ) with a simple conjugated diene under cycloaddition reaction conditions ; and.
In some embodiments the cycloaddition reaction is a [ 3 + 2 ] cycloaddition reaction.
The Diels-Alder reaction ( Scheme 9 ) is the cycloaddition reaction between a diene and a dienophile.
Step E involves the ( 2 + 3 ) cycloaddition reaction exactly in the same manner as described above.
Step C involves the ( 2 + 3 ) cycloaddition reaction between a nitrile oxide reagent and the substrate olefin 4.
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Examples of using Cycloaddition
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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