7. G. Tejeda, D. S. Belov, D. A. Fenoll, K. L. Rue, C. Tsay, X. Solans-Monfort, and K. V. Bukhryakov,* Vanadium Imido NHC Complexes for the Ring-Closing Olefin Metathesis Reactions, Organometallics, 2022, 41, 361-365. DOI: 10.1021/acs.organomet.2c00013

6. O. Alkhamis, J. Canoura, K. V. Bukhryakov, A. Tarifa, A. P. DeCaprio, and Y. Xiao,* DNA Aptamer-Cyanine Complexes as Generic Colorimetric Small-Molecule Sensors, Angew. Chem., Int. Ed., 2021, 60, 2-12. DOI: 10.1002/anie.202112305

5. D. S. Belov, D. A. Fenoll, I. Chakraborty, X. Solans-Monfort, and K. V. Bukhryakov,* Synthesis of Vanadium Oxo Alkylidene Complex and its Reactivity in Ring-Closing Olefin Metathesis Reactions, Organometallics, 2021, 40, 2939–2944. DOI: 10.1021/acs.organomet.1c00425

4. D. S. Belov, G. Tejeda, and K. V. Bukhryakov,* Olefin Metathesis by First-Row Transition Metals (invited review), ChemPlusChem, 2021, 86, 924-937. DOI: 10.1002/cplu.202100192

3. D. S. Belov, G. Tejeda, C. Tsay, and K. V. Bukhryakov,* Ring-Closing Olefin Metathesis Catalyzed by Well-Defined Vanadium Alkylidene Complexes, Chem. Eur. J, 2021, 27, 4578-4582. DOI: 10.1002/chem.202005438

2. D. S. Belov, L. Mathivathanan, M. J. Beazley, W. B. Martin, and K. V. Bukhryakov,* Stereospecific Ring-Opening Metathesis Polymerization of Norbornene Catalyzed by Iron Complexes, Angew. Chem., Int. Ed., 2021, 60, 2934-2938. DOI: 10.1002/anie.202011150 (highlighted in ChemistryViews).

1. S. Chuprun, C. M. Acosta, L. Mathivathanan, and K. V. Bukhryakov,* Molybdenum Benzylidyne Complexes for Olefin Metathesis Reactions, Organometallics, 2020, 39, 3453-3457. DOI: 10.1021/acs.organomet.0c00491

Before FIU

Postdoctoral research (MIT):

25. F. Zhai, K. V. Bukhryakov, R. R. Schrock, A. Hoveyda, C. Tsay, and P. Müller, Syntheses of Molybdenum Охо Benzylidene Complexes, J. Am. Chem. Soc., 2018, 140, 13609-13613. DOI: 10.1021/jacs.8b09616

24. K. V. Bukhryakov, R. R. Schrock, A. Hoveyda, C. Tsay, and P. Müller, Syntheses of Molybdenum Охо Alkylidene Complexes Through Addition of Water to an Alkylidyne Complex, J. Am. Chem. Soc., 2018, 140, 2797-2800. DOI: 10.1021/jacs.8b00499

23. K. V. Bukhryakov, S. VenkatRamani, C. Tsay, A. Hoveyda, and R. R. Schrock, Syntheses of Molybdenum Adamantylimido and t-Butylimido Alkylidene Chloride Complexes Using HCl and Diphenylmethylphosphine, Organometallics, 2017, 36, 4208-4214. DOI: 10.1021/acs.organomet.7b00647

22. P. E. Sues, K. V. Bukhryakov, and R. R. Schrock, Evaluation of Several Molybdenum and Ruthenium Catalysts for the Matathesis Homocoupling of 3-Methyl-1-Butene, Helv. Chim. Acta, 2017, 100, e1700181. DOI: 10.1002/hlca.201700181

21. K. V. Bukhryakov, R. R. Schrock, A. Hoveyda, P. Müller, and J. Becker, Synthesis of 2,6-Hexatertiarybutylterphenyl Derivatives, 2,6-(2,4,6-t-Bu3C6H2)2C6H3X, where X = I, Li, OH, SH, N3, or NH2, Org. Lett., 2017, 19, 2607-2609. DOI: 10.1021/acs.orglett.7b01062

20. J. K. Lam, C. Zhu, K. V. Bukhryakov, P. Müller, A. Hoveyda, and R. R. Schrock, Synthesis and Evaluation of Molybdenum and Tungsten Monoaryloxide Halide Alkylidene Complexes for Z-Selective Cross-Metathesis of Cyclooctene and Z-1,2- Dichloroethylene, J. Am. Chem. Soc., 2016, 138, 15774-15783. DOI: 10.1021/jacs.6b10499

19. P. E. Sues, J. M. John, K. V. Bukhryakov, R. R. Schrock, and P. Müller, Molybdenum and Tungsten Alkylidene Complexes That Contain a 2-Pyridyl-substituted Phenoxide Ligand, Organometallics, 2016, 35, 3587-3593. DOI: 10.1021/acs.organomet.6b00644

Postdoctoral research (KAUST):

18. T. Chen, B. Chen, K. V. Bukhryakov, and V. O. Rodionov, Thiols Make for Better Catalyst: Au Nanoparticles Supported on Functional SBA-15 for Catalysis of Ullmann-type Homocouplings, Chem. Commun., 2017, 53, 11638-11641. DOI: 10.1039/C7CC06146C

17. K. B. Vu, T. Chen, S. Almahdali, K. V. Bukhryakov, and V. O. Rodionov, Hollow Nanospheres with Fluorous Interiors for Transport of Molecular Oxygen in Water, ChemistrySelect, 2016, 1, 3306-3309. DOI: 10.1002/slct.201600602

16. K. V. Bukhryakov, V. G. Desyatkin, and V. O. Rodionov, Cooperative Organocatalysis of Mukaiyama–Type Aldol Reactions by Thioureas and Nitro Compounds, Chem. Commun., 2016, 52, 7576-7579. DOI: 10.1039/C6CC01984F

15. C. Mugemana, K. V. Bukhryakov, O. Bertrand, K. B. Vu, J.-F. Gohy, N. Hadjichristidis, V. O. Rodionov, Ring opening metathesis polymerization of cyclopentene using a ruthenium catalyst confined by a branched polymer architecture, Polym. Chem., 2016, 7, 2923-2928. DOI: 10.1039/C6PY00389C

14. K. V. Bukhryakov, C. Mugemana, K. B. Vu, V. O. Rodionov, Palladium-N-Heterocyclic Carbene Pre-Catalyst Site-Isolated in the Core of a Star Polymer, Org. Lett., 2015, 17, 4826-4829 DOI: 10.1021/acs.orglett.5b02388 (selected by the Editorial Board of Synfacts for its important insights, Synfacts, 2016, 12, 99 DOI: 10.1055/s-0035-1561082).

13. K. B. Vu, K. V. Bukhryakov, D. H. Anjum, V. O. Rodionov, Surface-Bound Ligands Modulate Chemoselectivity and Activity of a Bimetallic Nanoparticle Catalyst, ACS Catal., 2015, 5, 2529-2533 (K. B. Vu and K. V. Bukhryakov contributed equally). DOI: 10.1021/acscatal.5b00262

12. K. V. Bukhryakov, S. Almahdali, and V. O. Rodionov, Amplification of Chirality through Self-Replication of Micellar Aggregates in Water, Langmuir, 2015, 31, 2931-2935. DOI: 10.1021/la504984j

11. B. Chen, K. V. Bukhryakov, R. Sougrat, and V. Rodionov, An Enzyme-Inspired Functional Surfactant for Aerobic Oxidation of Activated Alcohols to Aldehydes in Water, ACS Catal., 2015, 5, 1313-1317. DOI: 10.1021/cs5020018

10. K. V. Bukhryakov, V. G. Desyatkin, J. P. O’Shea, S. R. Almahdali, V. Solovyeva, and V. Rodionov, Cooperative Catalysis With Block Copolymer Micelles: A Combinatorial Approach, ACS Comb. Sci., 2015, 17, 76-80 DOI: 10.1021/co5001713 (selected as ACS Editors’ Choice article, Jan. 13, 2015 and highlighted in C&EN, Jan. 19, 2015)

9. C. Mugemana, B. Chen, K. V. Bukhryakov, and V. Rodionov, Star Block-Copolymers: Enzyme-Inspired Catalysts for Oxidation of Alcohols in Water, Chem. Commun., 2014, 50, 7862-7865. DOI: 10.1039/C4CC03370A

Ph.D. research (MSU and CDI):

8. K. V. Bukhryakov, A. V. Kurkin, M. A. Yurovskaya, Synthesis of Imidazo[4,5-b]pyridines with a Chiral Substituent at the Nitrogen Atom and their Conversion to Piperazine Derivatives, Chem. Heterocycl. Compd. (N.Y.), 2012, 48, 773-784. DOI: 10.1007/s10593-012-1056-5

7. K. V. Bukhryakov, A. V. Kurkin, and M. A. Yurovskaya, Synthetic Approaches to Imidazo[4,5-b]pyridine Derivatives (review), Chem. Heterocycl. Compd. (N.Y.), 2011, 47, 533-557. DOI: 10.1007/s10593-011-0797-x

6. A. V. Kurkin, K. V. Bukhryakov, M. A. Yurovskaya, Synthesis of 1,2,3,4-tetrahydro[2,3-b]pyrazindiones with a Chiral Substituent at the Nitrogen, Chem. Heterocycl. Compd. (N.Y.), 2009, 45, 188-193. DOI: 10.1007/s10593-009-0249-z

5. I. Konstantinov, K. Bukhryakov, Y. Gezentsvey, and M. Krasavin, Practical Method for Parallel Synthesis of Diversely Substituted 1-Phenylpiperazines, Lett. Org. Chem., 2011, 8, 628-630. DOI: 10.2174/157017811799304386

4. M. Krasavin, V. Parchinsky, S. Shkavrov, and K. Bukhryakov, Applications of Quinoxaline Synthesis via Isocyanide-Based MCR. Multi-Component Reactions in Drug Discovery, Adv. Exp. Med. Bio, 2011, 699, 88-89. DOI: 10.1007/978-1-4419-7270-5_3

3. M. Krasavin, R. Karapetian, I. Konstantinov, Y. Gezentsvey, K. Bukhryakov, E. Godovykh, O. Soldatkina, Y. Lavrovsky, A.V. Sosnov, A.A. Gakh, Discovery and Potency Optimization of 2-Amino-5-arylmethyl-1,3-thiazole Derivatives as Potential Therapeutic Agents for Prostate Cancer, Arch. Pharm., 2009, 342, 420-427. DOI: 10.1002/ardp.200800201

2. M. Krasavin, S. Shkavrov, V. Parchinsky, and K. Bukhryakov, Imidazo[1,2-a]quinoxalines Accessed via Two Sequential Isocyanide-Based Multicomponent Reactions, J. Org. Chem., 2009, 74, 2627-2629. DOI: 10.1021/jo900050

1.M. Krasavin, S. Tsirulnikov, M. Nikulnikov, Y. Sandulenko, and K. Bukhryakov, tert-Butyl Isocyanide Revisited as a Convertible Reagent in the Groebke–Blackburn Reaction, Tetrahedron Lett., 2008, 49, 7318-7321. DOI: 10.1016/j.tetlet.2008.10.046