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Chemical Communications (Cambridge, England)|March 15, 2018
A rhodium-catalyzed transannulation of N-(per)fluoroalkyl-1,2,3-triazoles under microwave conditions - a general route to N-(per)fluoroalkyl-substituted five-membered heterocyclesVladimir Motornov, Athanasios Markos, Petr BeierThe Journal of Organic Chemistry|January 22, 2026
Synthesis of 2-Fluoroalkylated Pyridines and Fluoropyridines by Thermal Denitrogenation of N-Fluoroalkyl-1,2,3-triazoles and Cyclization of KeteniminesSvatava Voltrová, Blanka Klepetářová, Petr BeierBeilstein Journal of Organic Chemistry|December 14, 2017
One-pot three-component route for the synthesis of S-trifluoromethyl dithiocarbamates using Togni's reagentAzim Ziyaei Halimehjani, Martin Dračínský, Petr BeierThe Journal of Organic Chemistry|April 26, 2018
Transition-Metal-Free Coupling Reaction of Dithiocarbamates with Indoles: C-S Bond FormationAzim Ziyaei Halimehjani, Sahar Shokrgozar, Petr BeierChemical Communications (Cambridge, England)|July 11, 2023
N-Acyl-1,2,3-triazoles - key intermediates in denitrogenative transformationsVladimir Motornov, Radek Pohl, Blanka Klepetářová, et al.The Journal of Organic Chemistry|December 29, 2022
Lewis-Acid-Mediated Intramolecular Cyclization of 4-Aryl-5-allyl-1,2,3-triazoles to Substituted Cyclopentene DerivativesLukáš Janecký, Athanasios Markos, Blanka Klepetářová, et al.Organic & Biomolecular Chemistry|November 23, 2019
Synthesis of water-soluble hypervalent iodine reagents for fluoroalkylation of biological thiolsIveta Klimánková, Martin Hubálek, Václav Matoušek, et al.Beilstein Journal of Organic Chemistry|March 16, 2016
Synthesis and nucleophilic aromatic substitution of 3-fluoro-5-nitro-1-(pentafluorosulfanyl)benzeneJavier Ajenjo, Martin Greenhall, Camillo Zarantonello, et al.Organic Letters|November 1, 2016
Nucleophilic Tetrafluoroethylation Employing in Situ Formed Organomagnesium ReagentsAlena Budinská, Jiří Václavík, Václav Matoušek, et al.Organic Letters|February 24, 2011
S(N)Ar reactions of nitro-(pentafluorosulfanyl)benzenes to generate SF5 aryl ethers and sulfidesPetr Beier, Tereza Pastýříková, Norbert Vida, et al.Pageof 22