Diazoalkane 1,3-dipolar cycloaddition

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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.

The reaction product of a cycloaddition between diazomethane and trans-diethyl glutaconate is a 1-pyrazoline ^[1]. 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.

[edit] References

• ↑  Aza analogs of kainoids by dipolar cycloaddition Mingping Di and Kathleen S. Rein Tetrahedron Letters Volume 45, Issue 24 , 7 June 2004, Pages 4703-4705 Abstract Article