Photoinduced radical alkylation of aldehydes with potassium alkyltrifluoroborates

K. A. Zhilyaev, M. O. Zubkov, M. D. Kosobokov, V. V. Levin, A. D. Dilman

Org. Chem. Front. 2024, ASAP

https://doi.org/10.1039/D4QO00741G

 

One-Step Transformation of Aryl Diazonium Salts into Aryl Indium(III) Reagents

V. I. Supranovich, V. V. Levin, A. D. Dilman

Org. Lett. 2024, 26, 4537–4541

https://doi.org/10.1021/acs.orglett.4c01448

Complexes of Borane and 1,3,5-Triazinane-Derived Carbenes

V. O. Smirnov, V. V. Levin, A. D. Dilman

Adv. Synth. Catal. 2024, ASAP

https://doi.org/10.1002/adsc.202400122

Synthesis of N-(iminyl)pyridinium salts from hydrazones by the Zincke reaction

E. A. Ilin, V. O. Smirnov, A. D. Dilman

Russ. Chem. Bull. 2024, 73, 1297-1302

 

Dual Acridine/Decatungstate Photocatalysis for the Decarboxylative Radical Addition of Carboxylic Acids to Azomethines

Z. M. Rubanov, V. V. Levin, A. D. Dilman

Org. Lett. 2024, 26, 3174–3178

https://doi.org/10.1021/acs.orglett.4c00778

Radical reactions enabled by polyfluoroaryl fragments: photocatalysis and beyond

M. O. Zubkov, A. D. Dilman

Chem. Soc. Rev. 2024, 53, 4741 - 4785

https://doi.org/10.1039/D3CS00889D

Tetrafluoropyridinyl Thiolate as a Tool for Enabling Photoredox Alkylation of 1,2,4-Oxadiazoles

A. E. Frumkin, V. V. Levin, A. D. Dilman

Adv. Synth. Catal. 2024, ASAP

https://doi.org/10.1002/adsc.202400075

Practical photocatalytic hydroalkylation of alkenes with chloroacetates mediated by the formate ion

E. V. Malakhova, V. S. Kostromitin, V. V. Levin, A. D. Dilman

Org. Chem. Front. 2024, 11, 2829-2833

https://doi.org/10.1039/D4QO00228H

Direct conversion of carboxylic acids to free thiols via radical relay acridine photocatalysis enabled by N–O bond cleavage

D. L. Lipilin, M. O. Zubkov, M. D. Kosobokov, A. D. Dilman

Chem. Sci. 2024, 15, 644-650

https://doi.org/10.1039/D3SC05513B

One-Pot Transformation of Aldehydes to Ketones via Minisci-Type Reaction of Imines

Z. M. Rubanov, V. V. Levin, A. D. Dilman

Org. Lett. 2023, 25, 8751–8755

https://doi.org/10.1021/acs.orglett.3c03764

gem-Difluoroolefination of Amides

A. L. Trifonov, A. D. Dilman

Chem. Eur. J. 2023, e202303144

https://doi.org/10.1002/chem.202303144

Radical Substitution of Polyfluoroarenes and Heteroarenes Promoted by Photoredox Activation of Organozinc Iodides

A. A. Gladkov, V. V. Levin, A. D. Dilman

Adv. Synth. Catal. 2023, 19, 3387-3391

https://doi.org/10.1002/adsc.202300757

Photocatalytic Reaction of Aryl Halides with Tin(II) Acetate to Generate Arylstannane(IV) Reagents

A. A. Zemtsov, V. I. Supranovich, V. V. Levin, A. D. Dilman

ACS Catal. 2023, 13, 12766–12773

https://doi.org/10.1021/acscatal.3c03626

C–F Activation of Fluorinated Esters Using Photocatalytically Generated Diaminoalkyl Radical

V. S. Kostromitin, A. O. Sorokin, V. V. Levin, A. D. Dilman

Org. Lett. 2023, 25, 6598–6602

https://doi.org/10.1021/acs.orglett.3c02570

Zinc Chelate Complexes of N-Acyl Hydrazones as Substrates for Addition of Alkyl and Fluorinated Radicals

Z. M. Rubanov, V. V. Levin, A. D. Dilman

Adv. Synth. Catal. 2023, 15, 2636-2642

https://doi.org/10.1002/adsc.202300606

Atom Transfer Radical Addition via Dual Photoredox/Manganese Catalytic System

V. S. Kostromitin, V. V. Levin, A. D. Dilman

Catalysts. 2023, 13, 1126

https://doi.org/10.3390/catal13071126

 

Visible light-induced thiocyanation of gem-difluorinated phosphonium salts

G. A. Lozhkin, A. L. Trifonov, A. D. Dilman

Mendeleev Commun. 2023, 33, 491-493

https://doi.org/10.1016/j.mencom.2023.06.016

BF2-Chelates of N-Acylhydrazones as Versatile Coupling Partners in Photoredox Promoted Reactions

Z. M. Rubanov, V. I. Supranovich, V. V. Levin, A. D. Dilman

Eur. J. Org. Chem. 2023, 26, e202300247

https://doi.org/10.1002/ejoc.202300247

Sulfones Bearing Perfluorinated Pyridine Group: Synthesis and Photocatalytic Reaction with α-(Trifluoromethyl)styrenes

A. G. Savchenko, M. O. Zubkov, V. A. Kokorekin, J. Hu, A. D. Dilman

ChemCatChem 2023, 15, e202300505

https://doi.org/10.1002/cctc.202300505

Photocatalytic reduction of fluoroalkyl-substituted alcohols activated by pentafluoropyridine

S. L. Lunkov, A. A. Zemtsov, V. V. Levin, A. D. Dilman

Mendeleev Commun. 2023, 33, 387–389

https://doi.org/10.1016/j.mencom.2023.04.028

Dual Photoredox/Copper Catalyzed Fluoroalkylative Alkene Difunctionalization

V. S. Kostromitin, V. V. Levin, A. D. Dilman

J. Org. Chem. 2023, 88, 6252–6262

https://doi.org/10.1021/acs.joc.3c00448

Visible-Light Promoted Radical Fluoroalkylation of O- and N-Substituted Alkenes

V. V. Levin, A. D. Dilman

Chem. Rec. 2023, 23, e202300038

https://doi.org/10.1002/tcr.202300038

Aminals as powerful XAT-reagents: activation of fluorinated alkyl chlorides

V. S. Kostromitin, A. O. Sorokin, V. V. Levin, A. D. Dilman

Chem. Sci. 2023, 14, 3229–3234

https://doi.org/10.1039/D3SC00027C

Photoredox Promoted Barbier-Type Reaction of Alkyl Iodides with N-Alkyl and N-Aryl Imines

A. A. Gladkov, V. V. Levin, A. D. Dilman

J. Org. Chem. 2023, 88, 1260–1269

https://doi.org/10.1021/acs.joc.2c02598

Photocatalytic reactions of fluoroalkyl iodides with alkenes

G. I. Chernov, V. V. Levin, A. D. Dilman

Russ. Chem. Bull. 2023, 72, 61-72

https://doi.org/10.1007/s11172-023-3714-4

Organophotoredox-Catalyzed Reductive Tetrafluoroalkylation of Alkenes

V. S. Kostromitin, V. V. Levin, A. D. Dilman

J. Org. Chem. 2023, 88, 6523–6531

https://doi.org/10.1021/acs.joc.2c00712

Light-Promoted Dearylation of Perfluorinated Aryl Sulfides with N-Heterocyclic Carbene–Borane

L. I. Panferova, M. O. Zubkov, M. D. Kosobokov, A. D. Dilman

Org. Lett. 2022, 24, 8559–8563

https://doi.org/10.1021/acs.orglett.2c03585

Novel fluorescent difluoroboryl chelate complexes derived from N-benzothiazolyl hydrazones

Z. M. Rubanov, V. V. Levin, V. A. Kokorekin, A. D. Dilman

Tetrahedron Lett. 2022, 108, 154154

https://doi.org/10.1016/j.tetlet.2022.154154

Generation of fluoro(thio)carbenes from Me3SiCF2SAr

E. A. Ilin, V. O. Smirnov, A. D. Dilman

J. Fluorine Chem. 2022, 261-262, 110025

https://doi.org/10.1016/j.jfluchem.2022.110025

Preparation and Evaluation of Sterically Hindered Acridine Photocatalysts

K. A. Zhilyaev, D. L. Lipilin, M. D. Kosobokov, A. I. Samigullina, A. D. Dilman

Adv. Synth. Catal. 2022, 364, 3295–3301

https://doi.org/10.1002/adsc.202200515

Photocatalyzed Decarboxylative Thiolation of Carboxylic Acids Enabled by Fluorinated Disulfide

M. O. Zubkov, M. D. Kosobokov, V. V. Levin, A. D. Dilman

Org. Lett. 2022, 24, 2354–2358

https://doi.org/10.1021/acs.orglett.2c00549

Allylic substitution reactions with fluorinated nucleophiles

A. A. Zemtsov, V. V. Levin, A. D. Dilman

Coord. Chem. Rev. 2022459, 214455

https://doi.org/10.1016/j.ccr.2022.214455

Photocatalytic Alkylation of α-(Trifluoromethyl)Styrenes with Potassium Xanthogenates

V. I. Supranovich, A. D. Dilman

Catalysts 202111, 1555

https://doi.org/10.3390/catal11121555

Photoredox Activation of Organozinc Reagents: Barbier-Type Reaction of Alkyl Halides with α-(Trifluoromethyl)styrenes

A. A. Gladkov, G. N. Chernov, V. V. Levin, V. A. Kokorekin, A. D. Dilman

Org. Lett. 2021, 23, 9645-9648

https://doi.org/10.1021/acs.orglett.1c03917

Boron Chelates Derived from N-Acylhydrazones as Radical Acceptors: Photocatalyzed Coupling of Hydrazones with Carboxylic Acids

I. A. Dmitriev, V. V. Levin, A. D. Dilman

Org. Lett. 2021, 23, 8973-8977

https://doi.org/10.1021/acs.orglett.1c03501

Photocatalytic Atom-Transfer Radical Addition of Activated Chlorides to Alkenes

V. S. Kostromitin, A. A. Zemtsov, V. V. Levin, A. D. Dilman

Adv. Synth. Catal. 2021, 363, 5336–5340

https://doi.org/10.1002/adsc.202101047

Synthesis of Difluoroalkylated Heteroarenes via Difluorocarbene

A. L. Trifonov, A. D. Dilman

Org. Lett. 2021, 23, 6977–6981

https://doi.org/10.1021/acs.orglett.1c02603

One-pot synthesis of α-trifluoromethylstyrenes from aryl ketones and the Ruppert–Prakash reagent

V. V. Levin, A. D. Dilman

Mendeleev Commun. 2021, 31, 684–685

https://doi.org/10.1016/j.mencom.2021.09.030

Radical Functionalization of Geminal Difluoroalkenes

M. O. Zubkov, M. D. Kosobokov, A. D. Dilman

Russ. J. Org. Chem. 2021, 57, 1017–1035

https://doi.org/10.1134/S1070428021070010

Reaction of (bromodifluoromethyl)trimethylsilane with HMPA: Structural studies

V. I. Supranovich, A. D. Volodin, A. A. Korlyukov, J. Hu, A. D. Dilman

J. Fluorine Chem. 2021, 250, 109881

https://doi.org/10.1016/j.jfluchem.2021.109881

Generation of Alkyl Radicals from Thiols via Zinc Thiolates: Application for the Synthesis of gem-Difluorostyrenes

V. I. Supranovich, V. V. Levin, V. A. Kokorekin, A. D. Dilman

Adv. Synth. Cat. 2021, 363, 2888–2892

https://doi.org/10.1002/adsc.202100088

Light-Mediated Sulfur–Boron Exchange

L. I. Panferova, A. D. Dilman

Org. Lett. 2021, 23, 3919-3922

https://doi.org/10.1021/acs.orglett.1c01080

Photoredox Catalyzed Dealkylative Aromatic Halogen Substitution with Tertiary Amines

D. L. Lipilin, A. E. Frumkin, A. Y. Tyurin, V. V. Levin, A. D. Dilman

Atom-transfer radical addition of fluoroalkyl bromides to alkenes via a photoredox/copper catalytic system

V. S. Kostromitin, A. A. Zemtsov, V. A. Kokorekin, V. V. Levin, A. D. Dilman

Chem. Commun. 2021, 57, 5219-5222

https://doi.org/10.1039/D1CC01609A

Visible-Light-Promoted Reversible Sulfide/Iodide Exchange in Fluoroalkyl Sulfides Enabled by Electron Donor-Acceptor Complex Formation

B. A. van der Worp, M. D. Kosobokov, A. D. Dilman

ChemPhotoChem 2021, 5, 565-57

https://doi.org/10.1002/cptc.202100042

All-carbon phosphoranes via difluorocarbene trapping

V. O. Smirnov, A. D. Volodin, A. A. Korlyukov, A. D. Dilman

Chem. Commun. 2021, 57, 4823-4826

https://doi.org/10.1039/D1CC01075A

Photoredox Fluoroalkylation of Hydrazones in Neutral and Reductive Modes

B. A. van der Worp, M. D. Kosobokov, V. V. Levin, A. D. Dilman

Adv. Synth. Cat. 2021, 363, 1152-1158

https://doi.org/10.1002/adsc.202001381

Synthesis of Trifluoromethylated Dithiocarbamates via Photocatalyzed Substitution Reaction: Pentafluoropyridine as Activating Reagent

A. A. Zemtsov, S. S. Lunkov, V. V. Levin, A. D. Dilman

Eur. J. Org. Chem. 2021, 1007-1010

https://doi.org/10.1002/ejoc.202001572

Using the Thiyl Radical for Aliphatic Hydrogen-Atom Transfer: Thiolation of Unactivated C-H Bonds

L. I. Panferova, M. O. Zubkov, V. A. Kokorekin, V. V. Levin, A. D. Dilman

Angew. Chem. Int. Ed. 2021, 60, 2849–2854

https://doi.org/10.1002/anie.202011400

Alkene homologation via visible light promoted hydrophosphination using triphenylphosphonium triflate

V. V. Levin, A. D. Dilman

Chem. Commun. 2021, 57, 749–752

https://doi.org/10.1039/D0CC07025D

Synthesis of tetrafluorinated piperidines from nitrones via a visible-light-promoted annelation reaction

V. I. Supranovich, I. A. Dmitriev, A. D. Dilman

Beilstein J. Org. Chem. 2020, 16, 3104–3108

https://doi.org/10.3762/bjoc.16.260

Fluoroalkyl sulfides as photoredox-active coupling reagents for alkene difunctionalization

M. D. Kosobokov, M. O. Zubkov, V. V. Levin, V. A. Kokorekin, A. D. Dilman

Chem. Commun. 2020, 56, 9453–9456

https://doi.org/10.1039/D0CC04617E

ortho-Dialkylamino arylboranes as efficient reagents for difluorocarbene trapping

E. A. Ilin, V. O. Smirnov, A. D. Volodin, A. A. Korlyukov, A. D. Dilman

Chem. Commun. 2020, 56, 7140–7142

https://doi.org/10.1039/D0CC02567D

Visible-Light-Promoted Iododifluoromethylation of Alkenes via (Phosphonio)difluoromethyl Radical Cation

A. L. Trifonov, L. I. Panferova, V. V. Levin, V. A. Kokorekin, A. D. Dilman

Org. Lett. 2020, 22, 2409-2413

https://doi.org/10.1021/acs.orglett.0c00604

Trapping of Difluorocarbene by Frustrated Lewis Pairs

V. O. Smirnov, A. D. Volodin, A. A. Korlyukov, A. D. Dilman

Angew. Chem. Int. Ed. 2020, 59, 12428–1243

https://doi.org/10.1002/anie.202001354

Photoredox Fluoroalkylation of Arylidene and Alkylidene Amidrazones

V. I. Supranovich, G. N. Chernov, V. V. Levin, A. D. Dilman

Eur. J. Org. Chem. 2020, 393-396

https://doi.org/10.1002/ejoc.201901672

A novel photoredox-active group for the generation of fluorinated radicals from difluorostyrenes

M. O. Zubkov, M. D. Kosobokov, V. V. Levin, V. A. Kokorekin, A. A. Korlyukov, J. Hu, A. D. Dilman

Chem. Sci. 2020, 11, 737-741

https://doi.org/10.1039/C9SC04643G

Photoredox-catalyzed silyldifluoromethylation of silyl enol ethers

V. I. Supranovich, V. V. Levin, A. D. Dilman

Beilstein J. Org. Chem. 2020, 16, 1550-1553

https://doi.org/10.3762/bjoc.16.126

Visible-Light-Mediated Organocatalyzed Thiol-Ene Reaction Initiated by a Proton-Coupled Electron Transfer

V. V. Levin, A. D. Dilman

J. Org. Chem. 2019, 84, 8337-8343

https://doi.org/10.1021/acs.joc.9b01331

Light-Mediated Dual Phosphine-/Copper-Catalyzed Atom Transfer Radical Addition Reaction

O. V. Fedorov, S. I. Scherbinina, V. V. Levin, A. D. Dilman

J. Org. Chem. 2019, 84, 11068-11079

https://doi.org/10.1021/acs.joc.9b01649

Synthesis of tetrafluorinated tetrahydroquinolines via photoredox catalysis

V. I. Supranovich, A. D. Dilman

Mendeleev Commun., 2019, 29, 515–516

https://doi.org/10.1016/j.mencom.2019.09.012

Interaction of difluoromethylene phosphobetaine with heteroatom-centered electrophiles

A. L. Trifonov, L. I. Panferova, V. V. Levin, A. D. Volodin, A. A. Korlyukov, A. D. Dilman

J. Fluorine Chem. 2019, 220, 78–82

https://doi.org/10.1016/j.jfluchem.2019.02.008

Photoredox Reaction of 2-Mercaptothiazolinium Salts with Silyl Enol Ethers

A. A. Zemtsov, S. S. Ashirbaev, V. V. Levin, V. A. Kokorekin, A. A. Korlyukov, A. D. Dilman

J. Org. Chem. 2019, 84, 15745-15753

https://doi.org/10.1021/acs.joc.9b02478

Light-mediated copper-catalyzed phosphorus/halogen exchange in 1,1-difluoroalkylphosphonium salts

L. I. Panferova, V. V. Levin, M. I. Struchkova, A. D. Dilman

Chem. Commun. 2019, 55, 1314–1317

https://doi.org/10.1039/C8CC09115C

Reductive Bromodifluoromethylation of Nitrones Promoted by Visible Light

I. A. Dmitriev, V. I. Supranovich, V. V. Levin, A. D. Dilman

Eur. J. Org. Chem. 2019, 4119-4122

https://doi.org/10.1002/ejoc.201900274

Radical Addition to N-Tosylimines via C–H Activation Induced by Decatungstate Photocatalyst

V. I. Supranovich, V. V. Levin, A. D. Dilman

Org. Lett. 2019, 21, 4271–4274

https://doi.org/10.1021/acs.orglett.9b01450

Photoredox generation of the trifluoromethyl radical from borate complexes via single electron reduction

V. O. Smirnov, A. S. Maslov, V. A. Kokorekin, A. A. Korlyukov, A. D. Dilman

Chem. Commun. 2018, 54, 2236–2239

https://doi.org/10.1039/C8CC00245B

Photoredox mediated annelation of iododifluoromethylated alcohols with 1,1-diarylethylenes

L. I. Panferova, G. N. Chernov, V. V. Levin, V. A. Kokorekin, A. D. Dilman

Tetrahedron 2018, 74, 7136–7142

https://doi.org/10.1016/j.tet.2018.10.062

Photocatalytic Reductive Fluoroalkylation of Nitrones

V. I. Supranovich, V. V. Levin, M. I. Struchkova, A. D. Dilman

Org. Lett. 2018, 20, 840-843

https://doi.org/10.1021/acs.orglett.7b03987

Visible Light Promoted 2-Bromotetrafluoroethylation of Nitrones

I. A. Dmitriev, V. I. Supranovich, V. V. Levin, M. I. Struchkova, A. D. Dilman

Adv. Synth. Cat. 2018, 360, 3788-3792

https://doi.org/10.1002/adsc.201800802

Visible light-mediated difluoroalkylation of electron-deficient alkenes

V. I. Supranovich, V. V. Levin, M. I. Struchkova, J. Hu, A. D. Dilman

Beilstein J. Org. Chem. 2018, 14, 1637-1641

https://doi.org/10.3762/bjoc.14.139

Difluorocarbene as a Building Block for Consecutive Bond-Forming Reactions

A. D. Dilman, V. V. Levin

Acc. Chem. Res. 2018, 51, 1272–1280

https://doi.org/10.1021/acs.accounts.8b00079

Reductive silylation of gem-difluorinated phosphonium salts

A. V. Tsymbal, V. V. Levin, M. I. Struchkova, V. A. Kokorekin, A. A. Korlyukov, A. D. Dilman

J. Fluorine Chem. 2018, 205, 58-61

https://doi.org/10.1016/j.jfluchem.2017.11.009

Light-Promoted Allylation of Iododifluoromethylated Alcohols

L. I. Panferova, M. I. Struchkova, A.D. Dilman

Eur. J. Org. Chem. 2018, 3834-3836

https://doi.org/10.1002/ejoc.201800543

Synthesis of halodifluoromethyl-substituted phosphines

R. O. Iakovenko, A. D. Dilman

Mendeleev Commun. 2018, 28, 396-397

https://doi.org/10.1016/j.mencom.2018.07.018

Dimerization of Benzyl and Allyl Halides via Photoredox-Mediated Disproportionation of Organozinc Reagents

V. V. Levin, D. P. Agababyan, M. I. Struchkova, A. D. Dilman

Synthesis 2018, 50, 2930-2935

https://doi.org/10.1055/s-0036-1591583

Copper-Catalyzed Coupling of Acyl Chlorides with gem-Difluorinated Organozinc Reagents via Acyl Dithiocarbamates

S. S. Ashirbaev, V. V. Levin, M. I. Struchkova, A. D. Dilman

J. Org. Chem. 2018, 83, 478-483

https://doi.org/10.1021/acs.joc.7b02598

Addition of thiols to gem-difluoroalkenes under photoactivation conditions

S. S. Ashirbaev, V. V. Levin, M. I. Struchkova, A. D. Dilman

Vinylation of Iododifluoromethylated Alcohols via a Light-Promoted Intramolecular Atom-Transfer Reaction

L. I. Panferova, M. I. Struchkova, A. D. Dilman

Synthesis 2017, 49, 4124–4132

https://doi.org/10.1055/s-0036-1590855

Radical Silyldifluoromethylation of Electron-Deficient Alkenes

V. I. Supranovich, V. V. Levin, M. I. Struchkova, A. A. Korlyukov, A. D. Dilman

Org. Lett. 2017, 19, 3215–3218

https://doi.org/10.1021/acs.orglett.7b01334

Synthesis of 3-Fluoroindoles via Photoredox Catalysis

L. I. Panferova, V. O. Smirnov, V. V. Levin, V. A. Kokorekin, M. I. Struchkova, A. D. Dilman

J. Org. Chem. 2017, 82, 745-753

https://doi.org/10.1021/acs.joc.6b02344

Interaction of gem-Difluorinated Iodides with Silyl Enol Ethers Mediated by Photoredox Catalysis

G. N. Chernov, V. V. Levin, V. A. Kokorekin, M. I. Struchkova, A. D. Dilman

Adv. Synth. Cat. 2017, 359, 3063–3067

https://doi.org/10.1002/adsc.201700423

Synthesis of 3-Fluoropyridines via Photoredox-Mediated Coupling of α,α-Difluoro-β-iodoketones with Silyl Enol Ethers

S. I. Scherbinina, O. V. Fedorov, V. V. Levin, V. A. Kokorekin, M. I. Struchkova, A. D. Dilman

J. Org. Chem. 2017, 82, 12967-12974

https://doi.org/10.1021/acs.joc.7b02467

Difluoromethylation of Carboxylic Acids via the Addition of Difluorinated Phosphorus Ylide to Acyl Chlorides

A. L. Trifonov, V. V. Levin, M. I. Struchkova, A. D. Dilman

Org. Lett. 2017, 19, 5304–5307

https://doi.org/10.1021/acs.orglett.7b02601

Synthesis of gem-Difluorinated Hydroxypyrrolidines

O. V. Fedorov, M. I. Struchkova, A. D. Dilman

J. Org. Chem. 2017, 82, 3270–327

https://doi.org/10.1021/acs.joc.6b03033

Coupling of N-acyliminium chlorides with gem-difluorinated organozinc reagents

V. V. Levin, M. I. Struchkova, A. D. Dilman

Mendeleev Commun., 2017, 27, 139–140.

https://doi.org/10.1016/j.mencom.2017.03.010

Coupling of gem-difluorinated organozinc reagents with S-electrophiles

S. S. Ashirbaev, V. V. Levin, M. I. Struchkova, A. D. Dilman

J. Fluorine Chem. 2016, 191, 143-148

https://doi.org/10.1016/j.jfluchem.2016.07.018

Silicon Reagent with Functionalized Tetrafluoroethylene Fragments: Preparation and Coupling with Aldehydes

O. V. Fedorov, M. I. Struchkova, A. D. Dilman

J. Org. Chem. 2016, 81, 9455-946

https://doi.org/10.1021/acs.joc.6b01739

Advances in the chemistry of organozinc reagents

A. D. Dilman, V. V. Levin

Tetrahedron Letters 2016, 57, 3986-3992.

https://doi.org/10.1016/j.tetlet.2016.07.080

Nucleophilic Difluoromethylation Using (Bromodifluoromethyl)trimethylsilane

A. L. Trifonov, A. A. Zemtsov, V. V. Levin, M. I. Struchkova, A. D. Dilman

Org. Lett. 2016, 18, 3458–3461

https://doi.org/10.1021/acs.orglett.6b01641

Synthesis of difluorosubstituted six-membered nitronates via an addition/substitution cascade

O. V. Fedorov, V. V. Levin, A. D. Volodin, M. I. Struchkova, A. A. Korlyukov, A. D. Dilman

Tetrahedron Lett. 2016, 57, 3639-3642

https://doi.org/10.1016/j.tetlet.2016.06.135

Reactions of gem-difluoro-substituted organozinc reagents with propargyl halides

A. A. Zemtsov, N. S. Kondratyev, V. V. Levin, M. I. Struchkova, A. D. Dilman

Russ. Chem. Bull. 2016, 65, 2760–2762

https://doi.org/10.1007/s11172-016-1649-8

Reactions of gem-Difluorinated Phosphonium Salts Induced by Light

L. I. Panferova, A. V. Tsymbal, V. V. Levin, M. I. Struchkova, A. D. Dilman

Org. Lett. 2016, 18, 996-999

https://doi.org/10.1021/acs.orglett.6b00117

Dithiocarbamate-substituted gem-difluorinated silicon reagent: generation and addition to aldehydes

A. S. Maslov, V. O. Smirnov, M. I. Struchkova, D. E. Arkhipov, A. D. Dilman

Tetrahedron Lett. 2015, 56, 5048–5050

https://doi.org/10.1016/j.tetlet.2015.07.018

Synthesis of S-difluoromethyl dithiocarbamates

V. O. Smirnov, A. S. Maslov, M. I. Struchkova, D. E. Arkhipov, A. D. Dilman

Mendeleev Commun., 2015, 25, 452–453

https://doi.org/10.1016/j.mencom.2015.11.018

Nucleophilic difluoro(trimethylsilyl)methylation of arylidene Meldrum's acids

A. D. Volodin, A. A. Zemtsov, V. V. Levin, M. I. Struchkova, A. D. Dilman

J. Fluorine Chem. 2015, 176, 57–60

https://doi.org/10.1016/j.jfluchem.2015.05.009

Reactions of organozinc reagents with potassium bromodifluoroacetate

V. V. Levin, A. A. Zemtsov, M. I. Struchkova, A. D. Dilman

J. Fluorine Chem. 2015, 171, 97–101

https://doi.org/10.1016/j.jfluchem.2014.08.021

Reaction of gem-difluorinated organozinc reagents with β-nitrostyrenes

N. S. Kondratyev, V. V. Levin, A. A. Zemtsov, M. I. Struchkova, A. D. Dilman

J. Fluorine Chem. 2015, 176, 89–92

https://doi.org/10.1016/j.jfluchem.2015.06.001

Synthesis of organofluorine compounds using α-fluorine-substituted silicon reagents

A. D. Dilman, Levin, V. V.

Mendeleev Commun., 2015, 25, 239–244

https://doi.org/10.1016/j.mencom.2015.07.001

Halogenative Difluorohomologation of Ketones

O. V. Fedorov, M. D. Kosobokov, V. V. Levin, M. I. Struchkova, A. D. Dilman

J. Org. Chem. 2015, 80, 5870–5876

https://doi.org/10.1021/acs.joc.5b00904

Difluorohomologation of Ketones

M. D. Kosobokov, V. V. Levin, M. I. Struchkova, A. D. Dilman

Org. Lett. 2015, 17, 760–763

https://doi.org/10.1021/acs.orglett.5b00097

Coupling of α, α-difluoro-substituted organozinc reagents with 1-bromoalkynes

A. A. Zemtsov, A. D. Volodin, V. V. Levin, M. I. Struchkova, A. D. Dilman

Beilstein J. Org. Chem. 2015, 11, 2145–2149

https://doi.org/10.3762/bjoc.11.231

Nucleophilic Iododifluoromethylation of Aldehydes Using Bromine/Iodine Exchange

V. V. Levin, V. O. Smirnov, M. I. Struchkova, A. D. Dilman

J. Org. Chem. 2015, 80, 9349-9353

https://doi.org/10.1021/acs.joc.5b01590

Difluoromethylene Phosphabetaine as an Equivalent of Difluoromethyl Carbanion

V. V. Levin, A. L. Trifonov, A. A. Zemtsov, M. I. Struchkova, D. E. Arkhipov, A. D. Dilman

Org. Lett. 2014, 16, 6256-6259

https://doi.org/10.1021/ol503225s

Nucleophilic Bromo- and Iododifluoromethylation of Aldehydes

M. D. Kosobokov, V. V. Levin, M. I. Struchkova, A. D. Dilman

Org. Lett. 2014, 16, 3784–3787

https://doi.org/10.1021/ol501674n

Synthesis of fluorinated 4-amino-5,6-dihydropyridin-2(1H)-ones

M. D. Kosobokov, M. I. Struchkova, A. D. Dilman

Russ. Chem. Bull. 201463, 549–551

https://doi.org/10.1007/s11172-014-0468-z

Geminal Silicon/Zinc Reagent as an Equivalent of Difluoromethylene Bis-carbanion

M. D. Kosobokov, V. V. Levin, A. A. Zemtsov, M. I. Struchkova, A. A. Korlyukov, D. E. Arkhipov, A. D. Dilman

Org. Lett. 2014, 16, 1438-1441

https://doi.org/10.1021/ol5002297

Reactions of 1,1-difluoroalkylzinc halides with chlorinating reagents

V. O. Smirnov, A. S. Maslov, V. V. Levin, M. I. Struchkova, A. D. Dilman

Russ. Chem. Bull. 2014, 63, 2564–2566

https://doi.org/10.1007/s11172-014-0778-1

Synthesis of gem-Difluorinated Nitroso Compounds

V. O. Smirnov, M. I. Struchkova, D. E. Arkhipov, A. A. Korlyukov, A. D. Dilman

J. Org. Chem. 2014, 79, 11819-11823

https://doi.org/10.1021/jo5023537

Copper-Catalyzed Allylation of α,α-Difluoro-Substituted Organozinc Reagents

A. A. Zemtsov, N. S. Kondratyev, V. V. Levin, M. I. Struchkova, A. D. Dilman

J. Org. Chem. 2014, 79, 818–822

https://doi.org/10.1021/jo4024705

Nucleophilic Bromodifluoromethylation of Iminium Ions

A. V. Tsymbal, M. D. Kosobokov, V. V. Levin, M. I. Struchkova, A. D. Dilman

J. Org. Chem. 2014, 79, 7831–7835

https://doi.org/10.1021/jo501644m

Reactions of Difluorocarbene with Organozinc Reagents

V. V. Levin, A. A. Zemtsov, M. I. Struchkova, A. D. Dilman

Org. Lett. 2013, 15, 917–919

https://doi.org/10.1021/ol400122k

Synthesis of fluorinated pyrimidinones

M. D. Kosobokov, M. I. Struchkova, D. E. Arkhipov, A. A. Korlyukov, A. D. Dilman

J. Fluorine Chem. 2013, 154, 73–79

https://doi.org/10.1016/j.jfluchem.2013.06.018

Nucleophilic fluoroalkylation of (bromomethyl)pinacolborane using silicon reagents

V. V. Levin, P. K. Elkin, M. I. Struchkova, A. D. Dilman

J. Fluorine Chem. 2013, 154, 43–46

https://doi.org/10.1016/j.jfluchem.2013.06.007

Reactions of Sulfur- and Phosphorus-Substituted Fluoroalkylating Silicon Reagents with Imines and Enamines under Acidic Conditions

M. D. Kosobokov, A. D. Dilman, M. I. Struchkova, P. A. Belyakov, J. Hu

J. Org. Chem. 2012, 77, 2080-2086

https://doi.org/10.1021/jo202669w

Three-component reactions of CF3-substituted boranes, ethyl diazoacetate and imines

P. K. Elkin, V. V. Levin, A. D. Dilman, M. I. Struchkova, D. E. Arkhipov, A. A. Korlyukov

Tetrahedron Lett. 2012, 53, 6216-6218

https://doi.org/10.1016/j.tetlet.2012.08.153

Nucleophilic Pentafluorophenylation of Nitroalkenes

N. S. Kondratyev, A. A. Zemtsov, V. V. Levin, A. D. Dilman, M. I. Struchkova

Synthesis 2012, 44, 2436-2440

https://doi.org/10.1055/s-0032-1316553

Difluoro(trimethylsilyl)acetonitrile: Synthesis and Fluoroalkylation Reactions

M. D. Kosobokov, A. D. Dilman, V. V. Levin, M. I. Struchkova

J. Org. Chem. 2012, 77, 5850-585

https://doi.org/10.1021/jo301094b

Reactions of CF3-substituted boranes with α-diazocarbonyl compounds

P. K. Elkin, V. V. Levin, A. D. Dilman, M. I. Struchkova, P. A. Belyakov, D. E. Arkhipov, A. A. Korlyukov, V. A. Tartakovsky

Tetrahedron Lett. 2011, 52, 5259-5263

https://doi.org/10.1016/j.tetlet.2011.07.141

Nucleophilic trifluoromethylation with organoboron reagents

V. V. Levin, A. D. Dilman, P. A. Belyakov, M. I. Struchkova, V. A. Tartakovsky

Tetrahedron Lett. 2011, 52, 281-284

https://doi.org/10.1016/j.tetlet.2010.11.025

Nucleophilic Trifluoromethylation of C=N Bonds

A. D. Dilman, V. V. Levin

Eur. J. Org. Chem. 2011, 831-841

https://doi.org/10.1002/ejoc.201001558

Reactions of fluorinated silanes with 2-nitrocinnamates

A. A. Zemtsov, V. V. Levin, A. D. Dilman, M. I. Struchkova, V. A. Tartakovsky

J. Fluorine Chem. 2011, 132, 378-381

https://doi.org/10.1016/j.jfluchem.2011.03.015

Reaction of Baylis–Hillman Adducts with Fluorinated Silanes

A. A. Zemtsov, V. V. Levin, A. D. Dilman, M. I. Struchkova, P. A. Belyakov, V. A. Tartakovsky, J. Hu

Eur. J. Org. Chem. 2010, 6779-6785

https://doi.org/10.1002/ejoc.201001051

Synthesis of CF3-substituted 1,2,3,4-tetrahydroisoquinolines and 1,2,3,6-tetrahydropyridines

I. Yu. Chernyshov,V. V. Levin, A. D. Dilman, P. A. Belyakov, M. I. Struchkova, V. A. Tartakovsky

Russ. Chem. Bull. 2010, 59, 2102–2107

https://doi.org/10.1007/s11172-010-0362-2

Fluorocyanation of Enamines

A. D. Dilman, P. A. Belyakov, M. I. Struchkova, D. E. Arkhipov, A. A. Korlyukov, V. A. Tartakovsky

J. Org. Chem. 2010, 75, 5367-5370

https://doi.org/10.1021/jo1008993

Chelation-assisted pentafluorophenylation of oximes

V. V. Levin, R. T. Gritsenko, A. D. Dilman, P. A. Belyakov, A. A. Korlyukov, D. E. Arkhipov, M. I. Struchkova, V. A. Tartakovsky

Mendeleev Commun. 2010, 20, 220-222

https://doi.org/10.1016/j.mencom.2010.06.013

Hydroxyl-directed trifluoromethylation of hydrazones

A. D. Dilman, V. V. Levin, P. A. Belyakov, A. A. Korlyukov, M. I. Struchkova, V. A. Tartakovsky

Mendeleev Commun. 2009, 19, 141-143

https://doi.org/10.1016/j.mencom.2009.05.009

Nucleophilic trifluoromethylation of arylidene Meldrum's acids

A. A. Zemtsov, V. V. Levin, A. D. Dilman, M. I. Struchkova, P. A. Belyakov, V. A. Tartakovsky

Tetrahedron Lett. 2009, 50, 2998-3000

https://doi.org/10.1016/j.tetlet.2009.03.188

Trifluoromethylation of enamines under acidic conditions

R. T. Gritsenko, V. V. Levin, A. D. Dilman, P. A. Belyakov, M. I. Struchkova, V. A. Tartakovsky

Tetrahedron Lett. 2009, 50, 2994-2997

https://doi.org/10.1016/j.tetlet.2009.03.187

Reaction of the Ruppert-Prakash reagent with perfluorosulfonic acids

V. V. Levin, A. D. Dilman, P. A. Belyakov, M. I. Struchkova, V. A. Tartakovsky

J. Fluorine Chem. 2009, 130, 667-670

https://doi.org/10.1016/j.jfluchem.2009.05.003

Trifluoromethylation of the amide group

V. V. Levin, M. A. Kozlov, A. D. Dilman, P. A. Belyakov, M. I. Struchkova, V. A. Tartakovsky

Russ. Chem. Bull., Int. Ed., 2009, 58, 484-486

https://doi.org/10.1007/s11172-010-0039-x

Nucleophilic trifluoromethylation of arylidenemalononitriles

A. D. Dilman, V. V. Levin, P. A. Belyakov, M. I. Struchkova, V. A. Tartakovsky

Tetrahedron Lett. 2008, 49, 4352

https://doi.org/10.1016/j.tetlet.2008.05.039

Nucleophilic fluoroalkylation of iminium salts

V. V. Levin, M. A. Kozlov, Y.-H. Song, A. D. Dilman, P. A. Belyakov, M. I. Struchkova, V. A. Tartakovsky

Tetrahedron Lett. 2008, 49, 310

https://doi.org/10.1016/j.jorganchem.2007.12.022

Nucleophilic Trifluoromethylation of Imines under Acidic Conditions

V. V. Levin, A. D. Dilman, P. A. Belyakov, M. I. Struchkova, V. A. Tartakovsky

Eur. J. Org. Chem. 2008, 5226

https://doi.org/10.1002/ejoc.200800820

Complexation of tris(pentafluorophenyl)silanes with neutral Lewis bases

A. D. Dilman, V. V. Levin, A. A. Korlyukov, P. A. Belyakov, M. I. Struchkova, M. Yu. Antipin, V. A. Tartakovsky

J. Organomet. Chem. 2008, 693, 1005

https://doi.org/10.1016/j.jorganchem.2007.12.022

Trifluoromethylation of N-Benzoylhydrazones

A. D. Dilman, D. E. Arkhipov, V. V. Levin, P. A. Belyakov, A. A. Korlyukov, M. I. Struchkova, V. A. Tartakovsky

J. Org. Chem., 2008, 73, 5643

https://doi.org/10.1021/jo800782w

 

Reaction of Formamides with Fluorotris(pentafluorophenyl)silane

V. V. Levin, A. D. Dilman, P. A. Belyakov, M. I. Struchkova

Russ. J. Org. Chem. 2008, 44, 472

https://doi.org/10.1134/S1070428008030287

Trifluoromethylation of Salicyl Aldimines

A. D. Dilman, D. E. Arkhipov, V. V. Levin, P. A. Belyakov, A. A. Korlyukov, M. I. Struchkova, V. A. Tartakovsky

J. Org. Chem., 2007, 72, 8604

https://doi.org/10.1021/jo701734d

Trifluoromethylation and pentafluorophenylation of enamines

A. D. Dilman, V. V. Gorokhov, P. A. Belyakov, M. I. Struchkova, V. A. Tartakovsky

Russ. Chem. Bull. 2007, 56, 1522–1525

https://doi.org/10.1007/s11172-007-0235-5

Synthesis of C6F5-substituted amines containing quaternary carbon atoms

A. D. Dilman, V. V. Levin, P. A. Belyakov, M. I. Struchkova, V. A. Tartakovsky

Synthesis  2006,  447

https://doi.org/10.1055/s-2006-926277

Activation of pentafluorophenylsilanes by weak Lewis bases in reaction with iminium cations

A. D. Dilman, V. V. Levin, M. Karni, Y. Apeloig

J. Org. Chem., 2006, 71, 7214

https://doi.org/10.1021/jo0606812

Pentafluorophenyltrifluorosilane in the silicon Mannich reaction

A. D. Dilman, V. V. Gorokhov, P. A. Belyakov, M. I. Struchkova, V. A. Tartakovsky

Tetrahedron Lett. 2006, 47, 6217

https://doi.org/10.1016/j.tetlet.2006.06.164

Synthesis of C6F5-Substituted Aminoethanols via Acetate Ion Mediated C6F5-Group Transfer Reaction

V. V. Levin, A. D. Dilman, P. A. Belyakov, A. A. Korlyukov, M. I. Struchkova, M. Y. Antipin, V. A. Tartakovsky

Chloride ion promoted nucleophilic pentafluorophenylation of imines

V. V. Levin, A. D. Dilman, P. A. Belyakov, M. I. Struchkova, V. A. Tartakovsky

Tetrahedron Lett. 2006, 47, 8959

https://doi.org/10.1016/j.tetlet.2006.10.019

Pentafluorophenylation of -aminoacrylates

V. V. Levin, A. D. Dilman, P. A. Belyakov, A. A. Korlyukov, M. I. Struchkova, V. A. Tartakovsky

Synthesis and structural characterization of carbon-centered tris(pentafluorophenyl)silyl derivatives

A. D. Dilman, D. E. Arkhipov, A. A. Korlyukov, V. P. Ananikov, V. M. Danilenko, V. A. Tartakovsky

J. Organomet. Chem. 2005, 690, 3680

https://doi.org/10.1016/j.jorganchem.2005.04.058

Synthesis of pentafluorophenylmethylamines via silicon Mannich reaction

A. D. Dilman, P. A. Belyakov, A. A. Korlyukov, M. I. Struchkova, V. A. Tartakovsky

Org. Lett. 2005, 7, 2913

https://doi.org/10.1021/ol050845l

On the interaction of silyl triflates with enamines: iminium ion formation vs. silylation

V. V. Levin, A. D. Dilman, P. A. Belyakov, A. A. Korlyukov, M. I. Struchkova, V. A. Tartakovsky

Tetrahedron Lett. 2005, 46, 3729

https://doi.org/10.1016/j.tetlet.2005.03.144

Tris(pentafluorophenyl)silyl triflate: synthesis and silylation of carbonyl compounds

A. D. Dilman, P. A. Belyakov, A. A. Korlyukov, V. A. Tartakovsky

Tetrahedron Lett. 2004, 45, 3741


https://doi.org/10.1016/j.tetlet.2004.03.090

Tris(pentafluorophenyl)silyl enol ethers: synthesis and aldol reactions

V. V. Levin, A. D. Dilman, P. A. Belyakov, A. A. Korlyukov, M. I. Struchkova, V. A. Tartakovsky

Tetrahedron Lett. 2004, 45, 3741


https://doi.org/10.1016/j.tetlet.2004.03.090

New approach for the synthesis of isoxazoline-N-oxides

R. A. Kunetsky, A. D. Dilman, S. L. Ioffe, M. I. Struchkova, Y. A. Strelenko, V. A. Tartakovsky

Org. Lett. 2003, 5, 4907-4909

A New Strategy for the Synthesis of γ-Nitro Alcohols from Aliphatic Nitro Compounds

R. A. Kunetsky, A. D. Dilman, K. P. Tsvaygboym, S. L. Ioffe, Yu. A. Strelenko, V. A. Tartakovsky

Synthesis, 2003, 1339-1346

Reactions of N,N-bis(silyloxy)enamines with sulfur-centered and sulfur-stabilised electrophiles

A. V. Ustinov, A. D. Dilman, S. L. Ioffe, Yu. A. Strelenko, W. A. Smit, V. A. Tartakovsky

Mendeleev Commun., 2003, 74-76

Carbon-carbon bond forming reactions mediated by silicon Lewis acids

A. D. Dilman, S. L. Ioffe

Chem. Rev. 2003, 103, 733-772

Химия N,N-бис(силилокси)енаминов. Сообщение 4. Изучение реакций N,N-бис(силилокси)енаминов с 1,3-дикарбонильными соединениями

А. В. Устинов, А. Д. Дильман, С. Л. Иоффе, П. А. Беляков, Ю. А. Стреленко

Изв. Акад. Наук., Сер. хим., 2002, 1343

Structure and stereodynamics of N,N-bis(silyloxy)enamines

A. A. Tishkov, A. D. Dilman, V. I. Faustov, A. A. Birukov, K. S. Lysenko, P. A. Belyakov, S. L. Ioffe, Yu. A. Strelenko, M. Yu. Antipin

J. Am. Chem. Soc., 2002, 124, 11358-11367

Силилирование как новая стратегия использования алифтических нитросоединений в органическом синтезе

В. А. Тартаковский, С. Л. Иоффе, А. Д. Дильман, А. А. Тишков

Изв. Акад. Наук., Сер. хим., 2001, 1850–1859

Determination of the nucleophilicities of N,N-bis(silyloxy)enamines

A. D. Dilman, S. L. Ioffe, H. Mayr

J. Org. Chem., 2001, 66, 3196–3200

Chemistry of N,N-bis(silyloxy)enamines. 3. N,N-Bis(silyloxy)enamines as β-C-nucleophiles in reaction with acetals mediated by trimethylsilyl trifluoromethanesulfonate

A. D. Dilman, I. M. Lyapkalo, S. L. Ioffe, Yu. A. Strelenko, V. A. Tartakovsky

J. Org. Chem., 2000, 65, 8826–8829

Synthesis of N,N-bis(silyloxy)enamines with functionalized double bond

A. D. Dilman, A. A. Tishkov, I. M. Lyapkalo, S. L. Ioffe, V. V. Kachala, Yu. A. Strelenko, V. A. Tartakovsky

J. Chem. Soc. Perkin Trans. 1, 2000, 2926–2929

Триметилсилильные производные алифатических нитросоединений в реакции α,β-C,C-кросс-сочетания

А. Д. Дильман, И. М. Ляпкало, С. Л. Иоффе, Ю. А. Стреленко, В. А. Тартаковский

Изв. Акад. Наук., Сер. хим., 2000, 876–880

N,N-Бис(трет-бутилдиметилсилилокси)аминобензол как новый синтетический эквивалент нитрозобензола

А. Д. Дильман, И. М. Ляпкало, П. А. Беляков, С. Л. Иоффе, Ю. А. Стреленко, В. А. Тартаковский

Изв. Акад. Наук., Сер. хим., 2000, 1659–1660

Chemistry of N,N-Bis(silyloxy)enamines. 1. Novel convenient method for the synthesis of β–nitro oximes by C,C-cross-coupling of terminal N,N-bis(silyloxy)enamines with nitronate anions

A. D. Dilman, I. M. Lyapkalo, S. L. Ioffe, Yu. A. Strelenko, V. A. Tartakovsky

Synthesis, 1999, 1767–1775

Взаимодействие нитронатов — производных нитроалканов — с некоторыми тиостабилизированными катионоидными интермедиатами

И. М. Ляпкало, М. И. Лазарева, А. Д. Дильман, С. Л. Иоффе, В. А. Смит

Изв. Акад. Наук., Сер. хим., 1999, 492–497

Тетраметилсилан как газ-реагент: масс-спектры эфиров нитрокарбоновых кислот и нитроспиртов

В. И. Каденцев, Н. Г. Колотыркина, А. А. Стомахин, О. С. Чижов, С. Л. Иоффе, И. М. Ляпкало, А. Д. Дильман, А. А. Тишков

Изв. Акад. Наук., Сер. хим., 1998, 1257–1259

Четырехкомпонентное сочетание по схеме последовательности AdE-реакций с участием аренсульфенилхлорида, двух алкилвиниловых эфиров и кремнийорганических π-доноров как метод получения полифункциональных соединений

М. И. Лазарева, Ю. К. Крыщенко, А. Д. Дильман, А. Хейфорд, Р. Кэйпл, В. А. Смит

Изв. Акад. Наук., Сер. хим., 1998, 924–932

Novel Convenient Method for the Synthesis of N,N-bis(trimethylsilyloxy)enamines

A. D. Dilman, A. A. Tishkov, I. M. Lyapkalo, S. L. Ioffe, Yu. A. Strelenko, V. A. Tartakovsky

Synthesis, 1998, 181–185

Trimethylsilyl derivatives of aliphatic nitro compounds in α,β-C,C-cross-coupling reactions

A. D. Dilman, I. M. Lyapkalo, Yu. A. Strelenko, S. L. Ioffe, V. A. Tartakovsky

Mendeleev Commun., 1997, 133–135

Trimethylsilyl Derivatives as Final Nucleophiles in the Tandem Sequence of an ArSCl Initiated AdE Reaction Resulting in the Synthesis of Polyfunctional Compounds

A. Hayford, M. Lovdahl, M. I. Lazareva, Yu. K. Kryschenko, T. Johnson, A. D. Dilman, I. P. Smoliakova, R. Caple,  W. A. Smit

Mendeleev Commun., 1997, 48–50

Синтез аномально устойчивого C-метоксикарбонил-N-(п-нитрофенил)нитрона

А. Д. Дильман, И. М. Ляпкало, С. Л. Иоффе, Ю. А. Стреленко, В. А. Тартаковский

Ж. Орг. Хим. 1996, 36, 463–464