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

0541477 - ÚOCHB 2022 RIV DE eng J - Článek v odborném periodiku
Bakhanovich, Olga - Khutorianskyi, Viktor V. - Motornov, Vladimir - Beier, Petr
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. Roč. 17, Feb 18 (2021), s. 504-509. ISSN 1860-5397. E-ISSN 1860-5397
Grant CEP: GA MŠMT LTAUSA18037
Institucionální podpora: RVO:61388963
Klíčová slova: pyrrole * transannulation * rhodium carbene * triazole
Obor OECD: Organic chemistry
Impakt faktor: 2.544, rok: 2021
Způsob publikování: Open access
https://doi.org/10.3762/bjoc.17.44

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.
Trvalý link: http://hdl.handle.net/11104/0319028