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Synthesis and crystal structure of hydrated μ-oxa­lato-bis­{bis­[3-methyl-5-(pyridin-2-yl)-1H-1,2,4-triazole]iron(II)} bis­(toluene­sulfonate) 2.75-hydrate

Acta Crystallogr E Crystallogr Commun 2022, 78, 829-832

DOI: 10.1107/S2056989022007460

Petrenko Y.; Bibik Y.; Khomenko D.; Doroshchuk R.; Gural'skiy I.; Shova S.; Lampeka R.; Raspertova I.

Three-Month Heterochronic Parabiosis Has a Deleterious Effect on the Lifespan of Young Animals, Without a Positive Effect for Old Animals

Rejuvenation Research 2022, 25 (4), 191-199

DOI: 10.1089/rej.2022.0029

Yankova T.; Dubiley T.; Shytikov D.; Pishel I.

Radical Complexes of Nickel(II)/Copper(II) and Redox Non-innocent MB-DIPY Ligands: Unusual Stability and Strong Near-Infrared Absorption at λmax ∼1300 nm

Chem. Eur. J. 2022, 28 (41), e202201181

DOI: 10.1002/chem.202201181

Zatsikha Y.; Shamova L.; Shepit M.; Berry S.; Thomas F.; Herbert D.; van Lierop J.; Nemykin V.

A Practical and Scalable Approach to Fluoro-Substituted Bicyclo[1.1.1]pentanes

Angew. Chem. Int. Ed. 2022, 61 (29), e202205103

DOI: 10.1002/anie.202205103

Bychek R.; Mykhailiuk P.

The Ukrainian Factor in Early-Stage Drug Discovery in the Context of Russian Invasion: The Case of Enamine Ltd

ACS Med. Chem. Lett. 2022, 13 (7), 992-996

DOI: 10.1021/acsmedchemlett.2c00211

Kondratov I.; Moroz Y.; Grygorenko O.; Tolmachev A.

Meso-Carbon Atom Nucleophilic Attack Susceptibility in the Sterically Strained Antiaromatic Bis-BODIPY Macrocycle and Extended Electron-Deficient BODIPY Precursor

Chemistry 2022, 28 (54), e202201261

DOI: 10.1002/chem.202201261

Zatsikha Y.; Schrage B.; Blesener T.; Harrison L.; Ziegler C.; Nemykin V.

Polymorphic transition due to grinding: the case of 3-[1-(tert-but­oxy­carbonyl)­azetidin-3-yl]-1,2-oxaz­ole-4-carb­oxy­lic acid

Acta Crystallogr. B: Struct. Sci. Cryst. Eng. Mater. 2022, 78, 510-519

DOI: 10.1107/S2052520622003900

Konovalova I.; Shaposhnyk A.; Baumer V.; Chalyk B.; Shishkina S.

Unexpected Isomerization of Oxetane-Carboxylic Acids

Org. Lett. 2022, 24 (26), 4722-4728

DOI: 10.1021/acs.orglett.2c01402

Chalyk B.; Grynyova A.; Filimonova K.; Rudenko T.; Dibchak D.; Mykhailiuk P.

Impact of Fluoroalkyl Substituents on Physicochemical Properties of Saturated Heterocyclic Amines

Chem. Eur. J. 2022, 28 (55), e202201601

DOI: 10.1002/chem.202201601

Melnykov K.; Tavlui O.; Skreminskiy A.; Kuchkovska Y.; Grygorenko O.

Rapid synthetic approaches to libraries of diversified 1,2-dihydrochromeno[2,3-c]pyrrole-3,9-diones and 3-(2-hydroxyphenyl)-4,5-dihydropyrrolo[3,4-c]pyrazol-6(1H)-ones

Mol. Divers. 2022, 26 (2), 1115-1128

DOI: 10.1007/s11030-021-10234-2

Vydzhak R.; Panchishin S.; Kachaeva M.; Pilyo S.; Moskvina V.; Shablykina O.; Kozytskiy A.; Brovarets V.

Drug building blocks and libraries at risk in Ukraine

Science 2022, 376 (6596), 929

DOI: 10.1126/science.abq7841

Kondratov I.; Moroz Y.; Irwin J.; Shoichet B.

Towards in vivo photomediated delivery of anticancer peptides: Insights from pharmacokinetic and -dynamic data

J. Photochem. Photobiol. B 2022, 233, 112479

DOI: 10.1016/j.jphotobiol.2022.112479

Komarov I.; Tolstanova G.; Kuznietsova H.; Dziubenko N.; Yanchuk P.; Shtanova L.; Veselsky S.; Garmanchuk L.; Khranovska N.; Gorbach O.; Dovbynchuk T.; Borysko P.; Babii O.; Schober T.; Ulrich A.; Afonin S.

Structure-based virtual screening and biological evaluation of novel inhibitors of mycobacterium Z-ring formation

J. Cell. Biochem. 2022, 123 (5), 852-862

DOI: 10.1002/jcb.30232

Rayevsky A., Samofalova D., Ishchenko L., Vygovska L., Mazur V., Labudzynskyi D., Borysov O., Spivak S., Ozheredov S., Bulgakov E., Stykhylias M., Blume Y., Karpov P.

A Close-up Look at the Chemical Space of Commercially Available Building Blocks for Medicinal Chemistry

J. Chem. Inf. Model. 2022, 62 (9), 2171-2185

DOI: 10.1021/acs.jcim.1c00811

Zabolotna Y.; Volochnyuk D.; Ryabukhin S.; Horvath D.; Gavrilenko K.; Marcou G.; Moroz Y.; Oksiuta O.; Varnek A.

SynthI: A New Open-Source Tool for Synthon-Based Library Design

J. Chem. Inf. Model. 2022, 62 (9), 2151-2163

DOI: 10.1021/acs.jcim.1c00754

Zabolotna Y.; Volochnyuk D.; Ryabukhin S.; Gavrylenko K.; Horvath D.; Klimchuk O.; Oksiuta O.; Marcou G.; Varnek A.

Synthesis, Properties and Biological Potential Some Condensed Derivatives 1,2,4-Triazole

Ankara Universitesi Eczacilik Fakultesi Dergisi 2022, 46 (2), 308-321

DOI: 10.33483/jfpau.971602

Gotsulya A.; Brytanova T.

Synthesis of alpha-C-Stereochemically Pure Secondary Sulfonamides

J. Org. Chem. 2022, 87 (9), 6237-6246

DOI: 10.1021/acs.joc.2c00480

Andriashvili V.; Zhersh S.; Tolmachev A.; Grygorenko O.

One-pot parallel synthesis of 1,3,5-trisubstituted 1,2,4-triazoles

Mol. Divers. 2022, 26 (2), 993-1004

DOI: 10.1007/s11030-021-10218-2

Radchenko D.; Naumchyk V.; Dziuba I.; Kyrylchuk A.; Gubina K.; Moroz Y.; Grygorenko O.

Effect of gem-Difluorination on the Key Physicochemical Properties Relevant to Medicinal Chemistry: The Case of Functionalized Cycloalkanes

Chem. Eur. J. 2022, 28 (19), e202200331

DOI: 10.1002/chem.202200331

Holovach S.; Dr. Melnykov K.P.; Skreminskiy A.; Herasymchuk M.; Tavlui O.; Aloshyn D.; Dr. Borysko P. et al.

Expanding the chemical space of 3(5)-functionalized 1,2,4-triazoles

Chem. Heterocycl. Compd. 2022, 58 (2-3), 116-128

DOI: 10.1007/s10593-022-03064-z

Khomenko D.; Doroshchuk R.; Ohorodnik Y.; Ivanova H.; Zakharchenko B.; Raspertova I.; Vaschenko O.; Dobrydnev A.; Grygorenko O.; Lampeka R.

A stereochemical journey around spirocyclic glutamic acid analogs

Org. Biomol. Chem. 2022, 20 (15), 3183-3200

DOI: 10.1039/d2ob00146b

Chernykh A.; Chernykh A.; Radchenko D.; Chheda P.; Rusanov E.; Grygorenko O.; Spies M.; Volochnyuk D.; Komarov I.

Expanding the Repertoire of Low-Molecular-Weight Pentafluorosulfanyl-Substituted Scaffolds

ChemMedChem 2022, 17 (7), e202100641

DOI: 10.1002/cmdc.202100641

Jose A.; Guest D.; LeGay R.; Tizzard G.; Coles S.; Derveni M.; Wright E.; Marrison L.; Lee A.; Morris A.; Robinson M.; von Delft F.; Fearon D.; Koekemoer L.; Matviuk T.; Aimon A.; Schofield C.; MallavT.; London N.; Greenland B.; Bagley M.; Spencer J.

Fluorine-Containing Prolines: Synthetic Strategies, Applications, and Opportunities

J. Org. Chem. 2022, 87 (11), 6961-7005

DOI: 10.1021/acs.joc.1c02956

Mykhailiuk P.

Computationally driven discovery of SARS-CoV-2 Mpro inhibitors: from design to experimental validation

Chem. Sci. 2022, 13, 3674-3687

DOI: 10.1039/d1sc05892d

El Khoury L.; Jing Z.; Cuzzolin A.; Deplano A.; Loco D.; Sattarov B.; Hedin F.; Wendeborn S.; Ho C.; El AhdabvD.; Jaffrelot Inizan T.; Sturlese M.; Sosic A. et al.

Synthesis and Antimicrobial Evaluation of 2-(6-Imidazo[1,2-a]pyridin-2-yl-5-methyl-2,4-dioxo-3-phenyl-3,4-dihydrothieno[2,3-d]pyrimidin-1(2H)-yl)-N-arylacetamide Derivatives

Molbank 2022, 2022 (1), M1331

DOI: 10.3390/m1331

Vlasov S. V.; Severina H. I.; Borysov O. V.; Krolenko K. Y.; Shynkarenko P. E.; Saidov N. B.; Vlasov V. S.; Georgiyants V. A.

Reductive Recyclization of sp3-Enriched Functionalized Isoxazolines into α-Hydroxy Lactams

J. Org. Chem. 2022, 87 (2), 1001–1018

DOI: 10.1021/acs.joc.1c02301

Chalyk B.; Khutorianskyi A.; Vashchenko B.; Danyleiko K.; Grynyova A.; Osipova A.; Kozytskiy A.; Syniuchenko D.; Tsymbaliuk A.; Gavrilenko K.; Biitseva A.; Volochnyuk D.; Komarov I.; Grygorenko O.

Synthon-based ligand discovery in virtual libraries of over 11 billion compounds

Nature 2022, 601 (7893), 452-459

DOI: 10.1038/s41586-021-04220-9

Sadybekov A.; Sadybekov A.; Liu Y.; Iliopoulos-Tsoutsouvas C.; Huang X.; Pickett J.; Houser B.; Patel N.; Tran N.; Tong F.; Zvonok N.; Jain M.; Savych O.; Radchenko D.; Nikas S.; Petasis N.; Moroz Y. et al.

Exploration of the Chemical Space of DNA-encoded Libraries

Mol Inform 2022, 41 (6), e2100289

DOI: 10.1002/minf.202100289

Pikalyova R.; Zabolotna Y.; Volochnyuk D.; Horvath D.; Marcou G.; Varnek A.

Synthesis of spirocyclic β‐ and γ‐sultams by one‐pot reductive cyclization of cyanoalkylsulfonyl fluorides

Eur. J. Org. Chem. 2021, 2021 (47), 6530‑6540

DOI: 10.1002/ejoc.202000351

Stepannikova K.; Vashchenko B.; Grygorenko O.; Gorichko M.; Cherepakha A.; Moroz Y.; Volovenko Y.; Zhersh S.

Heteroaliphatic Dimethylphosphine Oxide Building Blocks: Synthesis and Physico-Chemical Properties

Eur. J. Org. Chem. 2021, 2021 (47), 6591‑6603

DOI: 10.1002/ejoc.202100581

Fedyk A.; Slobodyanyuk E.; Stotska O.; Vashchenko B.; Volochnyuk D.; Sibgatulin D.; Tolmachev A.; Grygorenko O.

Functionalized 5-Amino-4-cyanoxazoles, their Hetero- and Macrocyclic Derivatives: Preparation and Synthetic Applications

Eur. J. Org. Chem. 2021, 2021 (47), 6511‑6523

DOI: 10.1002/ejoc.202100412

Merzhyievskyi D.; Shablykin O.; Shablykina O.; Kozytskiy A.; Rusanov E.; Moskvina V.; Brovarets V.

Emerging Building Blocks for Medicinal Chemistry: Recent Synthetic Advances

Eur. J. Org. Chem. 2021, 2021 (47), 6478-6510

DOI: 10.1002/ejoc.202100857

Grygorenko O.; Volochnyuk D.; Vashchenko B.

Multigram Synthesis of Advanced 6,6-Difluorospiro[3.3]heptane-derived Building Blocks

Eur. J. Org. Chem. 2021, 2021 (47), 6541-6550

DOI: 10.1002/ejoc.202000432

Olifir O.; Chernykh A.; Dobrydnev A.; Grygorenko O.; Moroz Y.; Voitenko Z.; Radchenko D.

Reaction of N,N-Disubstituted Polyfluoroalkanethioamides with Diazomethane: Entry to New Thiirane Derivatives

Eur. J. Org. Chem. 2021, 2021 (47), 6524-6529

DOI: 10.1002/ejoc.202001104

Shermolovich Y.; Khyzhan A.; Rusanov E.; Mazepa A.; Rakipov I.; Mykhaylychenko S.

Monoprotected Diamines Derived from 1,5-Disubstituted (Aza)spiro[2.3]hexane Scaffolds

Eur. J. Org. Chem. 2021, 2021 (47), 6570-6579

DOI: 10.1002/ejoc.202001614

Malashchuk A.; Chernykh A. V.; Perebyinis M. Y.; Komarov I. V.; Grygorenko O. O.

Monosubstituted 3,3-Difluorocyclopropenes as Bench-Stable Reagents: Scope and Limitations

Eur. J. Org. Chem. 2021, 2021 (47), 6604-6615

DOI: 10.1002/ejoc.202100921

Nosik P. S.; Pashko M. O.; Poturai A. S.; Kvasha D. A.; Pashenko A. E.; Rozhenko A. B.; Suikov S.; Volochnyuk D. M.; Ryabukhin S. V.; Yagupolskii Y. L.

Last of the gem-Difluorocycloalkanes 2: Synthesis of Fluorinated Cycloheptane Building Blocks

Eur. J. Org. Chem. 2021, 2021 (47), 6561-6569

DOI: 10.1002/ejoc.202001530

Herasymchuk M.; Melnykov K.; Yarmoliuk D.; Serhiichuk D.; Rotar V.; Pukhovoi T.; Kuchkovska Y.; Holovach S.; Volochnyuk D.; Ryabukhin S.; Grygorenko O.

Enamine Ltd.: The Science and Business of Organic Chemistry and Beyond

Eur. J. Org. Chem. 2021, 2021 (47), 6474-6477

DOI: 10.1002/ejoc.202101210

Grygorenko O.

Catalytic Hydrogenation of Substituted Quinolines on Co–Graphene Composites

Eur. J. Org. Chem. 2021, 2021 (47), 6616-6625

DOI: 10.1002/ejoc.202101311

Asaula V.; Buryanov V.; Solod B.; Tryus D.; Pariiska O.; Kotenko I.; Volovenko Y.; Volochnyuk D.; Ryabukhin S.; Kolotilov S.

Mononuclear π-complexes of Pd(II) and Pt(II) with 1-allyl-3-(2-hydroxyethyl)thiourea: Synthesis, structure, molecular docking, DNA binding ability and genotoxic activity

Polyhedron 2021, 210 115477

DOI: 10.1016/j.poly.2021.115477

Orysyk S. I.; Baranets S.; Borovyk P. V.; Palchykovska L. G.; Zborovskii Y. L.; Orysyk V. V.; Likhanov A. F.; Platonov M. O.; Kovalskyy D. B.; Shyryna T. V.; Danylenko Y.; Hurmach V. V.; Pekhnyo V. I.; Vovk M. V.

The PIFA-initiated oxidative cyclization of 2-(3-butenyl)quinazolin- 4(3H)-ones - an efficient approach to 1-(hydroxymethyl)- 2,3-dihydropyrrolo[1,2-a]quinazolin-5(1H)-ones

Beilstein J. Org. Chem. 2021, 17 2787-2794

DOI: 10.3762/bjoc.17.189

Vaskevych A. I.; Savinchuk N. O.; Vaskevych R. I.; Rusanov E. B.; Grygorenko O. O.; Vovk M. V.

Design, synthesis and in vitro antimicrobial activity of 6-(1H-benzimidazol-2-yl)-3,5-dimethyl-4-oxo-2-thio-3,4-dihy-drothieno[2,3-d]pyrimidines

Sci. Pharm. 2021, 89(4), 49

DOI: 10.3390/scipharm89040049

Vlasov S.; Vlasova O.; Severina H.; Krolenko K.; Borysov O.; Abu Sharkh A.; Vlasov V.; Georgiyants V.

Fluorenonophane chlorobenzene solvate: Molecular and crystal structures

Acta Cryst. 2021, 77, 1285-1288

DOI: 10.1107/S2056989021011865

Dyakonenko V.; Shishkina S.; Bogashchenko T.; Lyapunov A.; Kirichenko T.

Crystal structure and Hirshfeld surface analysis of di-μ-chlorido-bis[(acetonitrile-κN)chlorido(ethyl 5-methyl-1H-pyrazole-3-carboxylate-κ2N2,O)copper(II)]

Acta Cryst. 2021, 77, 1153-1157

DOI: 10.1107/S2056989021010653

Vynohradov O.; Pavlenko V.; Kucheriv O.; Golenya I.; Petlovanyi D.; Shova S.

Large-Scale Synthesis and Modifications of Bicyclo[1.1.1]pentane-1,3-dicarboxylic Acid (BCP)

J. Org. Chem. 2021, 86 (20), 14061–14068

DOI: 10.1021/acs.joc.1c00977

Ripenko V.; Vysochyn D.; Klymov I.; Zhersh S.; Mykhailiuk P.

Highly efficient synthesis and NMR features of novel fused pyrimidothiazinium trihalogenides

J. Heterocycl. Chem. 2021, 59 (2), 329-340

DOI: 10.1002/jhet.4387

Onysko M.; Svalyavin O.; Slivka M.; Slivka M.; Baumer V.; Lendel V.

In silico mechanistic model of microtubule assembly inhibition by selective chromone derivatives

J. Mol. Struct. 2021, 1241, 130633

DOI: 10.1016/j.molstruc.2021.130633

Rayevsky A.; Sharifi M.; Samofalova D.; Demchuk O.; Karpov P.; Blume Y.

Bicyclic Pyrrolidines for Medicinal Chemistry via [3 + 2]-Cycloaddition

J. Org. Chem. 2021, 86 (19), 13289–13309

DOI: 10.1002/slct.202001243

Savych V.; Mykhalchuk V.; Melnychuk P.; Isakov A.; Savchuk T.; Timoshenko V.; Siry S.; Pavlenko S.; Kovalenko D.; Hryshchuk O.; Reznik V.; Chalyk B.; Yarmolchuk V.; Rusanov E.

Fluorine-Labelled Spiro[3.3]heptane-Derived Building Blocks: Is Single Fluorine the Best?

Eur. J. Org. Chem. 2021, 2021 (35), 4897-4910

DOI: 10.1002/ejoc.202100804

Malashchuk A.; Chernykh A.; Dobrydnev A.; Grygorenko O.

4-(N-Boc-amino)-1Н-1,2,3-triazolecarbothioamides in the synthesis of a new heterocyclic [1,2,3]triazolo[4,5-e][1,4]thiazepine system

Chem. Heterocycl. Compd. 2021, 57 (7-8), 841-847

DOI: 10.1007/s10593-021-02989-1

Syrota N.; Kemskiy S.; Bol’but A.; Chernobaev I.; Liavinets O.; Vovk M.
 

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