Synthesis of N-perfluoroalkyl-3,4-disubstituted pyrroles by rhodium-catalyzed transannulation of N-fluoroalkyl-1,2,3-Triazoles with terminal alkynes

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Abstract

The rhodium-catalyzed transannulation of N-perfluoroalkyl-1,2,3-Triazoles with aromatic and aliphatic terminal alkynes under microwave heating conditions afforded N-perfluoroalkyl-3,4-disubstituted pyrroles (major products) and N-fluoroalkyl-2,4-disubstituted pyrroles (minor products). The observed selectivities in the case of the reactions with aliphatic alkynes were high.

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Bakhanovich, O., Khutorianskyi, V., Motornov, V., & Beier, P. (2021). Synthesis of N-perfluoroalkyl-3,4-disubstituted pyrroles by rhodium-catalyzed transannulation of N-fluoroalkyl-1,2,3-Triazoles with terminal alkynes. Beilstein Journal of Organic Chemistry, 17, 504–510. https://doi.org/10.3762/BJOC.17.44

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