Difference between revisions of "Template:Heidelberg/project/rd/copperclick"
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A highly energetic azide reacts with an alkyne enabling a selective reaction that links these reactive groups to one another via a dipolar cycloaddition (Fig. 1). However this reaction requires a lot of activation energy.<x-ref>zhang2005</x-ref> Without catalyst the reaction is slow and results in a 1,4, 1,5 triazole regioisomer. To increase the reaction rate and to avoid this byproduct it is necessary to add copper as a catalyst. Copper (Cu(I)) proofed to be a suitable catalyst that rapidly yields a 1,2,3 triazole heterocycle. | A highly energetic azide reacts with an alkyne enabling a selective reaction that links these reactive groups to one another via a dipolar cycloaddition (Fig. 1). However this reaction requires a lot of activation energy.<x-ref>zhang2005</x-ref> Without catalyst the reaction is slow and results in a 1,4, 1,5 triazole regioisomer. To increase the reaction rate and to avoid this byproduct it is necessary to add copper as a catalyst. Copper (Cu(I)) proofed to be a suitable catalyst that rapidly yields a 1,2,3 triazole heterocycle. | ||
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+ | The advantages of a click reaction are that it is very simple and works under many different conditions, as well as that the reaction results in high yields with no byproducts. The highly energetic azides react with alkynes enabling a selective reaction that links reactive groups to one another. To obtain the oxidation state of the copper sodium ascorbate is added to the reaction. Furthermore a ligand like THPTA is necessary to keep the Cu(I) stabilized in aqueous solution. | ||
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Revision as of 02:56, 19 September 2015
Copper-catalyzed azide-alkyne cycloaddition (CuAAC)
Sharpless described the copper-catalyzed azide-alkyne cycloaddition (CuAAC)
The advantages of a click reaction are that it is very simple and works under many different conditions, as well as that the reaction results in high yields with no byproducts. The highly energetic azides react with alkynes enabling a selective reaction that links reactive groups to one another. To obtain the oxidation state of the copper sodium ascorbate is added to the reaction. Furthermore a ligand like THPTA is necessary to keep the Cu(I) stabilized in aqueous solution.
In order to use the above explained advantages of click chemistry for the labelling of DNA and RNA azide or alkyne modified nucleotides have to be incorporated into the sequence (Fig. 2). Martin et al. have shown that yeast Poly(A) Polymerase is able to incorporate modified nucleotides with small moieties