A. Tabolin

发表

Nucleophilic Halogenation of Cyclic Nitronates: A General Access to 3-Halo-1,2-Oxazines.

Y. Nelyubina, V. A. Tartakovsky, A. Sukhorukov, 2019, The Journal of organic chemistry.

Deoxygenative Arylation of 5,6-Dihydro-4H-1,2-oxazine-N-oxides with Arynes.

Y. Nelyubina, A. Sukhorukov, S. Ioffe, 2022, The Journal of organic chemistry.

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 .

Small Ring Compounds and N‐oxides: Cycloadditions and Related Processes

S. Ioffe, A. Tabolin, 2016 .

Organofluorine chemistry: promising growth areas and challenges

V. M. Karpov, A. B. Koldobskii, S. N. Osipov, 2018, Russian Chemical Reviews.

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.

Rearrangement of N-oxyenamines and related reactions.

S. Ioffe, A. Tabolin, 2014, Chemical reviews.

Diels-Alder Reaction of β-Fluoro-β-nitrostyrenes. Synthesis of Mono-fluorinated Six-Membered Derivatives

V. Nenajdenko, S. Ioffe, A. Tabolin, 2020 .

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 .

Six-membered cyclic nitronates as 1,3-dipoles in formal [3 + 3]-cycloaddition with donor-acceptor cyclopropanes. Synthesis of new type of bicyclic nitrosoacetals.

Y. Nelyubina, Yu. V. Tomilov, S. Ioffe, 2013, Organic letters.

Recent Advances in the Synthesis and Chemistry of Nitronates

A. Sukhorukov, S. Ioffe, A. Dilman, 2017 .

Acylation of Nitronates: [3,3]-Sigmatropic Rearrangement of in Situ Generated N-Acyloxy, N-oxyenamines.

Y. Nelyubina, A. Sukhorukov, S. Ioffe, 2018, The Journal of organic chemistry.

Synthesis of unsaturated silyl nitronates via the silylation of conjugated nitroalkenes

Y. Nelyubina, S. Ioffe, R. Novikov, 2018, Tetrahedron Letters.

Tandem Pd-catalyzed C–C coupling/recyclization of 2-(2-bromoaryl)cyclopropane-1,1-dicarboxylates with primary nitro alkanes

Y. Nelyubina, S. Ioffe, R. Novikov, 2016 .

Six-Membered Cyclic Nitroso Acetals: Synthesis and Studies of the Nitrogen Inversion Process of N-Silyloxy-3,6-dihydro-2H-1,2-oxazines

Y. Nelyubina, S. Ioffe, R. Novikov, 2016 .

Six‐Membered Cyclic Nitronates as 1,3‐Dipoles in Formal [3 + 3]‐Cycloaddition with Donor—Acceptor Cyclopropanes. Synthesis of New Type of Bicyclic Nitrosoacetals.

Y. Nelyubina, Yu. V. Tomilov, S. Ioffe, 2013 .

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.

One-Pot Synthesis of 3-(2-Fluoroalkenyl)indoles

V. Nenajdenko, S. Ioffe, A. Tabolin, 2019, European Journal of Organic Chemistry.

Synthesis of α-Prolinols and 2-Amino-1,5-diols from Primary Nitroalkanes and Other Simple Precursors via Intermediacy of 5,6-Dihydro-4H-1,2-oxazines

S. Ioffe, Yulia A. Khomutova, A. Tabolin, 2012 .

Green, Catalyst-Free Reaction of Indoles with β-Fluoro-β-nitrostyrenes in Water

V. Nenajdenko, S. Ioffe, A. Tabolin, 2018, European Journal of Organic Chemistry.

An Easy Synthesis of Monofluorinated Derivatives of Pyrroles from β-Fluoro-β-Nitrostyrenes

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

Chlorination of Conjugated Nitroalkenes with PhICl2 and SO2Cl2 for the Synthesis of α-Chloronitroalkenes

S. Ioffe, A. Tabolin, A. A. Fadeeva, 2020, Synthesis.

Synthesis of Isoxazolines from Nitroalkanes via a [4+1]‐Annulation Strategy

Y. Nelyubina, A. Sukhorukov, S. Ioffe, 2019, Advanced Synthesis & Catalysis.

In Situ Generated Magnesium Cyanide as an Efficient Reagent for Nucleophilic Cyanation of Nitrosoalkenes and Parent Nitronates

A. Sukhorukov, S. Ioffe, A. Tabolin, 2019, European Journal of Organic Chemistry.

Tandem [3+2]-cycloaddition/homo-Baldwin rearrangement of silyl nitronates and donor-acceptor cyclopropenes. A novel approach to polysubstituted aziridines starting from nitro compounds

S. Ioffe, A. Tabolin, I. Golovanov, 2022, Tetrahedron.

Synthesis and chemical transformations of six/six-membered bicyclic nitroso acetals

Y. Nelyubina, S. Ioffe, R. Novikov, 2016, Russian Chemical Bulletin.

Formal [3+3]-cycloaddition of 3-methyl-5,6-dihydro-4H-1,2-oxazine-N-oxides with cyclopropane dicarboxylates under hyperbaric conditions

Y. Nelyubina, Yu. V. Tomilov, S. Ioffe, 2015 .

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.

Sequential Formal [4+1]‐Cycloaddition, C−H Functionalization and Suzuki–Miyaura Cross‐Coupling for the Synthesis of Trisubstituted Isoxazolines

A. Sukhorukov, S. Ioffe, A. Tabolin, 2021 .

Synthesis of phosphodiesterase IVb inhibitors 2. Stereoselective synthesis of hexahydro-3H-pyrrolo[1,2-c]imidazol-3-one and tetrahydro-1H-pyrrolo[1,2-c][1,3]oxazol-3-one derivatives

V. A. Tartakovsky, A. Sukhorukov, S. Ioffe, 2011 .

Rearrangement of 3-alkylidene-2-siloxy-tetrahydro-1,2-oxazines (ASENA). A new approach toward the synthesis of 3-α-hydroxyalkyl-5,6-dihydro-4H-1,2-oxazines

Y. Nelyubina, S. Ioffe, Yulia A. Khomutova, 2009 .

α-Electrophilic Reactivity of Nitronates.

A. Sukhorukov, S. Ioffe, A. Tabolin, 2018, Chemical record.

Sequential Acylation/Silylation/Hetero‐Claisen Rearrangement of Nitroalkanes for the Synthesis of Protected Hydroxyoxime Derivatives

A. Sukhorukov, S. Ioffe, A. Tabolin, 2021 .

Reactions of silyl nitronates with dimethylformamide dimethyl acetal as a new general procedure for the synthesis of 2-nitroenamines

S. Ioffe, Yulia A. Khomutova, A. Tabolin, 2014 .

Novel Formal [3+3] Cycloaddition of Silyl Nitronates with Activated Cyclopropanes and Its Application in the Synthesis of Pyrroline-N-oxides

Yu. V. Tomilov, S. Ioffe, Yulia A. Khomutova, 2014 .

Dehydration of isoxazoline N-oxides under electrophilic conditions – An alternative approach toward 3-haloisoxazoles

S. Ioffe, A. Tabolin, A. A. Fadeeva, 2021, Tetrahedron Letters.

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.

New Rearrangement of Conjugated Cyclic Ene Nitroso O‐Trimethylsilyl Acetals: Convenient Synthesis of Dihydro‐2H‐pyran‐3‐one and Dihydrofuran‐3‐one Oximes.

Y. Nelyubina, S. Ioffe, Yulia A. Khomutova, 2011 .

New Rearrangement of ConjugatedCyclic Ene Nitroso O-Trimethylsilyl Acetals:Convenient Synthesis of Dihydro-2H-pyran-3-oneand Dihydrofuran-3-one Oximes

Y. Nelyubina, S. Ioffe, Yulia A. Khomutova, 2011 .

[3+3]-Annulation of Cyclic Nitronates with Vinyl Diazoacetates: Diastereoselective Synthesis of Partially Saturated [1,2]Oxazino[2,3-b][1,2]oxazines and Their Base-Promoted Ring Contraction to Pyrrolo[1,2-b][1,2]oxazine Derivatives

Y. Nelyubina, S. Ioffe, A. Tabolin, 2023, Molecules.

Synthesis of 3‐Haloisoxazolines by Deoxygenation of 3‐Haloisoxazoline N ‐Oxides under Treatment with Acetyl Bromide

S. Ioffe, A. Tabolin, A. A. Fadeeva, 2022, ChemistrySelect.