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Diazoalkane 1,3-dipolar cycloaddition
The Diazoalkane 1,3-dipolar cycloaddition is a 1,3-dipolar cycloaddition (an organic reaction) between a 1,3-dipole diazo compound (notably diazomethane) and a dipolarophile. When the dipolarphile is an alkene, the reaction product is a pyrazoline.
Additional recommended knowledge
The reaction product of a cycloaddition between diazomethane and trans-diethyl glutaconate is a 1-pyrazoline. This reaction is 100% regioselective because the diazo terminal nitrogen atom bonds exclusively to the alpha-carbon of the ester. The reaction is also a syn addition, and the configuration in the dipolarophile is preserved. The 1-pyrazoline is unstable and isomerizes to the 2-pyrazoline due to favorable conjugation with the ester group.
With phenyldiazomethane as the reactant the regioselectivity is reversed and the reaction is extended even further by simple air organic oxidation of the 2-pyrazoline to the pyrazole.
Another example of a diazo cycloaddition is a diazo-thioketone coupling.
|This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Diazoalkane_1,3-dipolar_cycloaddition". A list of authors is available in Wikipedia.|