| Acetylene in organic synthesis: Recent progress and new uses VV Voronin, MS Ledovskaya, AS Bogachenkov, KS Rodygin, ... Molecules 23 (10), 2442, 2018 | 136 | 2018 |
| [3 + 2]-Cycloaddition of in Situ Generated Nitrile Imines and Acetylene for Assembling of 1,3-Disubstituted Pyrazoles with Quantitative Deuterium Labeling VV Voronin, MS Ledovskaya, EG Gordeev, KS Rodygin, VP Ananikov The Journal of Organic Chemistry 83 (7), 3819-3828, 2018 | 91 | 2018 |
| Calcium-mediated one-pot preparation of isoxazoles with deuterium incorporation MS Ledovskaya, KS Rodygin, VP Ananikov Organic Chemistry Frontiers 5 (2), 226-231, 2018 | 64 | 2018 |
| Calcium carbide: Versatile synthetic applications, green methodology and sustainability KS Rodygin, MS Ledovskaya, VV Voronin, KA Lotsman, VP Ananikov European Journal of Organic Chemistry 2021 (1), 43-52, 2021 | 59 | 2021 |
| Efficient labeling of organic molecules using 13 C elemental carbon: universal access to 13 C 2-labeled synthetic building blocks, polymers and pharmaceuticals MS Ledovskaya, VV Voronin, KS Rodygin, VP Ananikov Organic Chemistry Frontiers 7 (4), 638-647, 2020 | 46 | 2020 |
| Methods for the synthesis of O-, S-and N-vinyl derivatives MS Ledovskaya, VV Voronin, KS Rodygin Russian Chemical Reviews 87 (2), 167, 2018 | 45 | 2018 |
| Direct synthesis of deuterium-labeled O-, S-, N-vinyl derivatives from calcium carbide MS Ledovskaya, VV Voronin, KS Rodygin, AV Posvyatenko, KS Egorova, ... Synthesis 51 (15), 3001-3013, 2019 | 35 | 2019 |
| Examining the vinyl moiety as a protecting group for hydroxyl (–OH) functionality under basic conditions VV Voronin, MS Ledovskaya, KS Rodygin, VP Ananikov Organic Chemistry Frontiers 7 (11), 1334-1342, 2020 | 31 | 2020 |
| Direct Synthesis of 1-Arylprop-1-ynes with Calcium Carbide as an Acetylene Source L Gao, Z Li Synlett 30 (13), 1580-1584, 2019 | 25 | 2019 |
| Acetylene and ethylene: universal C2 molecular units in cycloaddition reactions MS Ledovskaya, VV Voronin, KS Rodygin, VP Ananikov Synthesis, 999-1042, 2021 | 19 | 2021 |
| Primary Vinyl Ethers as Acetylene Surrogate: A Flexible Tool for Deuterium‐Labeled Pyrazole Synthesis MS Ledovskaya, VV Voronin, MV Polynski, AN Lebedev, VP Ananikov European Journal of Organic Chemistry 2020 (29), 4571-4580, 2020 | 18 | 2020 |
| Synthesis of isoxazolopyrroloisoquinolines by intramolecular cyclizations of 5-(2-arylethyl)-6-hydroxytetrahydro-4H-pyrrolo [3, 4-d] isoxazol-4-ones AV Stepakov, MS Ledovskaya, VM Boitsov, AP Molchanov, RR Kostikov, ... Tetrahedron Letters 53 (40), 5414-5417, 2012 | 18 | 2012 |
| One‐Pot and Two‐Chamber Methodologies for Using Acetylene Surrogates in the Synthesis of Pyridazines and Their D‐Labeled Derivatives MS Ledovskaya, MV Polynski, VP Ananikov Chemistry–An Asian Journal 16 (16), 2286-2297, 2021 | 17 | 2021 |
| An efficient synthesis of substituted isoxazolopyrroloisoquinolines via diastereoselective N-acyliminium ion cyclization MS Ledovskaya, AP Molchanov, VM Boitsov, RR Kostikov, AV Stepakov Tetrahedron 71 (13), 1952-1958, 2015 | 17 | 2015 |
| An efficient synthesis of substituted spiro [isoxazolopyrroloisoquinolines] via diastereoselective N-acyliminium ion cyclization MS Ledovskaya, AV Stepakov, AP Molchanov, RR Kostikov Tetrahedron 71 (40), 7562-7566, 2015 | 15 | 2015 |
| Anthracene-fused isoxazolopyrrolo [2, 1-a] isoquinolines via an endocyclic N-acyliminium ion cyclization: a joint experimental and theoretical study MS Ledovskaya, AP Molchanov, RR Kostikov, TL Panikorovsky, ... Tetrahedron 72 (32), 4827-4834, 2016 | 13 | 2016 |
| Cycloaddition Reactions of in situ Generated C2D2 in Dioxane: Efficient Synthetic Approach to D2‐Labeled Nitrogen Heterocycles VV Voronin, MS Ledovskaya, KS Rodygin, VP Ananikov European Journal of Organic Chemistry 2021 (41), 5640-5648, 2021 | 12 | 2021 |
| Synthesis of glucosamine vinyl ether derivative and its deuterated analog KS Rodygin, VV Voronin, MS Ledovskaya Russian Chemical Bulletin 69, 1401-1404, 2020 | 11 | 2020 |
| Molybdenum-mediated one-pot synthesis of pyrazoles from isoxazoles M Rey, S Beaumont Synthesis 51 (20), 3796-3804, 2019 | 11 | 2019 |
| Molecules VV Voronin, MS Ledovskaya, AS Bogachenkov, KS Rodygin, ... | 6 | 2018 |
