Publications

22. A. R. Beisenbayev, I. Ivanov-Prianichnikov, A. Peshkov, T. Adil, D. Hayrapetyan, C.-K. Lim, Triple-Band Warm White-Light Emission from Type II Band-Aligned Aggregation-Induced Enhanced Emission Organic Cation-Incorporated Two-Dimensional Lead Iodide Perovskite. Int. J. Mol. Sci. 2025, 26, 5054.

21. K. Petrova, A. Kaipov, L. Yussupova, I. Iznat, D. Hayrapetyan, Decarboxylation of Aza-Annulation Products as a Synthetic Route to 3-Pyrrolin-2-ones and 1,2,3,4-Tetrahydropyridin-2-ones, J. Org. Chem. 2024, 89, 14596–14600.

20. D. Hayrapetyan, L. Yussupova, A. Kaipov and A. Galyamova, Electrochemical synthesis of spirocyclic morpholines and tetrahydrofurans via an oxidative dearomatisation strategy, Org. Biomol. Chem., 2023, 21, 7090-7094

19. K. Gudun, R. Zakarina, M. Segizbayev, D. Hayrapetyan, A. Slamova, A. Khalimon, Cobalt-Catalyzed Deoxygenative Hydroboration of Nitro Compounds and Applications to One-Pot Synthesis of Aldimines and Amides, Adv. Synth. Catal. 2022, 364, 601.

18. D. Baidilov, D. Hayrapetyan, A. Y. Khalimon, Recent advances in homogeneous base-metal-catalyzed transfer hydrogenation reactions, Tetrahedron 2021, 98, 132435.

17. D. Hayrapetyan, V. Stepanova, Facile Synthesis of Spirocyclic Lactams via [3+2] and [3+3] Aza‐Annulation Reactions, Eur. J. Org. Chem. 2021, 2121–2125.

16. Á. M. Martínez, D. Hayrapetyan, T. van Lingen, M. Dyga, L. J. Gooßen, Taking electrodecarboxylative etherification beyond Hofer–Moest using a radical C–O coupling strategy, Nature Commun. 2020, 11, 4407.

15. M. Segizbayev, Ö. Öztopçu, D. Hayrapetyan, D. Shakhman, K.A. Lyssenko, A. Y. Khalimon, Transfer Hydrogenation of Aldehydes and Ketones Catalyzed by an Aminophosphinite POCNH Pincer Complex of Ni(II), Dalton Transactions, 2020, 11950-11957

14. D. Hayrapetyan, A. Y. Khalimon, Catalytic Nitrile Hydroboration: A Route to N,N‐Diborylamines and Uses Thereof, Chem. Asian J. 2020, 15, 2575-2587.

13. K. A. Gudun, A. Slamova, D. Hayrapetyan, A.Y. Khalimon, Efficient Co‐catalyzed Double Hydroboration of Nitriles: Application to One‐Pot Conversion of Nitriles to Aldimines.  Chem. Eur. J. 2020, 26, 4963

• Highlighted in Synform (Synform 2020/09, A130–A132)

12. A. Y. Khalimon, K. A. Gudun, D. Hayrapetyan, Base Metal Catalysts for Deoxygenative Reduction of Amides to Amines, Catalysts 2019, 9(6), 490-516

11. Marco Dyga, Davit Hayrapetyan, Raja K. Rit, Lukas J. Gooßen, Electrochemical ipso-Thiocyanation of Arylboron Compounds, Adv. Synth. Catal. 2019, 361, 3548–3553

• Very Important Publication

10. D. Hayrapetyan, R. K. Rit, M. Kratz, K. Tschulik, L. J. Gooßen, Electrochemical C–H Cyanation of Electron-Rich (Hetero)Arenes, Chem. Eur. J., 2018, 24, 11288 – 11291

• Hot Paper

9.     E. A. Hall, J. E. Ramsey, Z. Peng, D. Hayrapetyan, V. Shkepu, B. O'Rourke, W. Geiger, K. Lam, C. F. Verschraegen, Novel organometallic chloroquine derivative inhibits tumor growth, J Cell Biochem. 2018; 119, 5921-5933

8.     D. Hayrapetyan, V. Shkepu, O. T. Seilkhanov, Z. Zhanabil, K. Lam, Electrochemical synthesis of phthalides via anodic activation of aromatic carboxylic acids, Chem. Commun., 2017, 53, 8451-8454

7.     H. Miyamura, A. Sonoyama, D. Hayrapetyan, S. Kobayashi, Self-Assembled Nanocomposite Organic Polymers with Aluminum and Scandium as Heterogeneous Water-Compatible Lewis Acid Catalysts, Angew. Chem. Int. Ed. 2015, 54, 10559 –10563

• Highlighted in Synfacts (Synfacts 2015, 11(12), 1331)

6.     A. Zherebker, D. Airapetyan, A. I. Konstantinov, Y. Kostyukevich, A. Kononikhin, I. Popov, K. V. Zaitsev, E. Nikolaev, I. V. Perminova, Synthesis of Model Humic Substances by Oxidative Coupling of Phenylpropanoic Monomer and Hydroquinone: Mechanistic Study Using Controllable H/D Exchange and Fourier Transform Ion Cyclotron Resonance Mass Spectrometry, Analyst, 2015, 140, 4708-4719

5.     D. V. Airapetyan, V. S. Petrosyan, S. V. Gruener, A. A. Korlyukov, D. E. Arkhipov, A. A. Bowden, K. V. Zaitsev, Structure of hypercoordinatedmonoorganodihalostannanes in solutions and in the solid state: the halogen effect, Inorg. Chim. Acta, 2015, 432,142-148

4.     D.V. Airapetyan, V.S. Petrosyan, S.V. Gruener, K.V. Zaitsev, D.E. Arkhipov, A.A. Korlyukov, Disproportionation reactions within the series of coordinated monoorganostannanes, J. Organomet. Chem., 2013, 747, 241-248.

3.     D. V. Airapetyan, T. P. Murasheva, S. Yu. Bylikin, A. A. Korlyukov, A. G. Shipov, S. V. Gruner, E. P. Kramarova, Vad. V. Negrebetsky, S. A. Pogozhykh, G. Ya. Zueva, M. Yu. Antipin. Yu. I. Baukov, Trichloro- and methyldichlorogermylmonochelates and dibromo- and dichlorogermylbischelates derived from N,N-disubstituted amides of 2-hydroxycarboxylic acids, Russ. Chem. Bull., 2012, 61, 642-651.

2.     S. V. Gruener, D. V. Airapetyan, A. A. Korlyukov, A. G. Shipov, Y. I. Baukov, V. S. Petrosyan, Interaction of ethyltrichlorostannane with N,N-dimethylamides of O-trimethylsilyl-α-hydroxyacids, Appl. Organomet. Chem., 2010, 24, 888-896.

1.     A. G. Shipov, S. V. Gruner, A. A. Korlyukov, E. P. Kramarova, T. P. Murasheva, S. Yu. Bylikin, Vad. V. Negrebetsky, F. A. Ivaschenko, D. V. Airapetyan, G. Ya. Zueva, M. Yu. Antipin. Yu. I. Baukov, Tribromogermyl monochelates — derivatives of N,N-disubstituted 2-hydroxycarboxylic amides, Russ. Chem. Bull., 2010, 59, 761-770.