An efficient synthesis of 1,3-diaryl-4-halo-1H-pyrazoles was achieved. The synthesis involves the [3 + 2] dipolar cycloaddition of 3-arylsydnones and 2-aryl-1,1-dihalo-1-alkenes. The process proceeds smoothly in moderate to excellent yields. 1,3-Diaryl-4-halo-1H-pyrazoles are found to be important intermediates that can easily be converted into 1,2,5-triaryl-substituted pyrazoles via Pd-catalyzed C-H bond activation. © 2011 Yang et al; licensee Beilstein-Institut.
CITATION STYLE
Yang, Y., Kuang, C., Jin, H., Yang, Q., & Zhang, Z. (2011). Efficient synthesis of 1,3-diaryl-4-halo-1 H-pyrazoles from 3-arylsydnones and 2-aryl-1,1-dihalo-1-alkenes. Beilstein Journal of Organic Chemistry, 7, 1656–1662. https://doi.org/10.3762/bjoc.7.195
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