Vladimir A. Motornov

发表

Copper-catalyzed [3 + 2]-cycloaddition of α-halonitroalkenes with azomethine ylides: facile synthesis of multisubstituted pyrrolidines and pyrroles.

Y. Nelyubina, V. Nenajdenko, S. Ioffe, 2021, Organic & biomolecular chemistry.

Fluoronitroalkenes in tandem [4 + 1]/[3 + 2]-cycloaddition: one-pot three-component assembly of fluorinated bicyclic nitroso acetals

Y. Nelyubina, V. Nenajdenko, S. Ioffe, 2018 .

Copper(I)‐Catalyzed Regioselective Chan‐Lam N 2‐Vinylation of 1,2,3‐Triazoles and Tetrazoles

I. Beletskaya, N. Lukashev, Vladimir A. Motornov, 2019, Advanced Synthesis & Catalysis.

Radical Nitration-Debromination of α-Bromo-α-fluoroalkenes as a Stereoselective Route to Aromatic α-Fluoronitroalkenes-Functionalized Fluorinated Building Blocks for Organic Synthesis.

Y. Nelyubina, V. Nenajdenko, S. Ioffe, 2017, The Journal of organic chemistry.

Access to Fluoroalkylated Azoles and 2-Acylaminoketones via Fluorinated Anhydride-Mediated Cleavage of NH-1,2,3-Triazoles.

P. Beier, Vladimir A. Motornov, 2022, Organic letters.

General approach to 2-fluoroalkyl 1,3-azolesviathe tandem ring opening and defluorinative annulation ofN-fluoroalkyl-1,2,3-triazoles

P. Beier, Vladimir A. Motornov, Vojtech Kostal, 2019, Organic Chemistry Frontiers.

Preparation of 1-Azido-2-bromo-1,1,2,2-tetrafluoroethane and its Use in the Synthesis of N-Fluoroalkylated Nitrogen Heterocycles.

P. Beier, Iveta Klimánková, D. Tichý, 2020, The Journal of organic chemistry.

Oxidative [3+2]-annulation of nitroalkenes and azolium ylides in the presence of Cu(II): efficient synthesis of [5,5]-annulated N-fused heterocycles

S. Ioffe, A. Tabolin, Vladimir A. Motornov, 2021, New Journal of Chemistry.

Copper-mediated oxidative [3 + 2]-annulation of nitroalkenes and pyridinium imines: efficient synthesis of 3-fluoro- and 3-nitro-pyrazolo[1,5-a]pyridines.

Y. Nelyubina, V. Nenajdenko, S. Ioffe, 2020, Organic & biomolecular chemistry.

Synthesis and Regioselective N‐2 Functionalization of 4‐Fluoro‐5‐aryl‐1,2,3‐NH‐triazoles

Y. Nelyubina, V. Nenajdenko, S. Ioffe, 2017 .

Acid‐Mediated Three Component Assembly of 4‐Fluoropyrazoles from α‐Fluoronitroalkenes, Hydrazines, and Aldehydes

Y. Nelyubina, V. Nenajdenko, S. Ioffe, 2020 .

Chemoselective Aza-[4+3]-annulation of N-Perfluoroalkyl-1,2,3-triazoles with 1,3-Dienes: Access to N-Perfluoroalkyl-Substituted Azepines.

P. Beier, Vladimir A. Motornov, 2018, The Journal of organic chemistry.

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 heterocycles.

P. Beier, Vladimir A. Motornov, Athanasios Markos, 2018, Chemical communications.

Copper-mediated oxidative [3 + 2]-annulation of nitroalkenes and pyridinium ylides: general access to functionalized indolizines and efficient synthesis of 1-fluoroindolizines.

Y. Nelyubina, V. Nenajdenko, S. Ioffe, 2019, Organic & biomolecular chemistry.

Copper‐Mediated Oxidative [3+2]‐Annulation of Nitroalkenes and Ylides of 1,2‐Diazines: Assembly of Functionalized Pyrrolo[1,2‐b]pyridazines

V. Nenajdenko, S. Ioffe, A. Tabolin, 2021, ChemistrySelect.

Stereoselective Synthesis of (Z)-β-Enamido Triflates and Fluorosulfonates from N-Fluoroalkylated Triazoles.

P. Beier, B. Klepetářová, S. Voltrová, 2019, Chemistry.

Synthesis of 2,5-diaryl-4-halo-1,2,3-triazoles and comparative study of their fluorescent properties

V. Nenajdenko, S. Ioffe, R. Novikov, 2018, Tetrahedron.

Synthesis of N-vinyl isothiocyanates and carbamates by the cleavage of NH-1,2,3-triazoles with one-carbon electrophiles.

P. Beier, Vladimir A. Motornov, 2023, Organic & biomolecular chemistry.

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

P. Beier, Vladimir A. Motornov, V. Khutorianskyi, 2021, Beilstein journal of organic chemistry.

Introducing Weakly Ligated Tris(trifluoromethyl)copper(III)

P. Slavíček, X. Ribas, P. Beier, 2024, ChemistryEurope.

N-Acyl-1,2,3-triazoles - key intermediates in denitrogenative transformations.

R. Pohl, P. Beier, B. Klepetářová, 2023, Chemical communications.