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  1. 2018

  2. A Comparative Study of Modern Homology Modeling Algorithms for Rhodopsin Structure Prediction.

    Nikolaev, D., Панов, М. С., Jamal, A., Кочемировский, В. А., Olivucci, M. & Рязанцев, М. Н., 31 Jul 2018, In: ACS Omega. 3, 7, p. 7555-7566 12 p.

    Research output: Contribution to journal › Article › peer-review

  3. Influence of the ligand nature on the in situ laser-induced synthesis of the electrocatalytically active copper microstructures

    Панов, М. С., Кочемировский, В. А., Рязанцев, М. Н., Тумкин, И. И., Хайруллина, Е. М., Балова, И. А., Логунов, Л. С. & Мюнд, Л. А., Jul 2018, In: Arabian Journal of Chemistry. 11, 5, p. 624-634 11 p.

    Research output: Contribution to journal › Article › peer-review

  4. A highly diastereoselective one-pot three-component 1,3-dipolar cycloaddition of cyclopropenes with azomethine ylides generated from 11H-indeno[1,2-b]-quinoxalin-11-ones.

    Филатов, А. С., Князев, Н. А., Рязанцев, М. Н., Суслонов, В. В., Ларина, А. Г., Молчанов, А. П., Костиков, Р. Р., Бойцов, В. М. & Степаков, А. В., 21 Feb 2018, In: Organic Chemistry Frontiers. 5, 4, p. 595-605 11 p.

    Research output: Contribution to journal › Article › peer-review

  5. New experimental models of retinal degeneration for screening molecular photochromic ion channel blockers

    Rotov, A. Y., Astakhova, L. A., Sitnikova, V. S., Evdokimov, A. A., Boitsov, V. M., Dubina, M. V., Ryazantsev, M. N. & Firsov, M. L., 1 Jan 2018, In: Acta Naturae. 10, 1, p. 75-84 10 p.

    Research output: Contribution to journal › Article › peer-review

  6. 2017

  7. Non-enzymatic sensors based on in situ laser-induced synthesis of copper gold and gold nano-sized microstructures

    Panov, M. S., Vereshchagina, O. A., Ermakov, S. S., Tumkin, I. I., Khairullina, E. M., Skripkin, M. Y., Mereshchenko, A. S., Ryazantsev, M. N. & Kochemirovsky, V. A., 15 May 2017, In: Talanta. 167, p. 201-207 7 p.

    Research output: Contribution to journal › Article › peer-review

  8. A voltage-dependent fluorescent indicator for optogenetic applications, archaerhodopsin-3: Structure and optical properties from in silico modeling

    Ryazantsev, M. N., Николаев, Д. М., Emelyanov, A., Boitsov, V. M. & Panov, M. S., 2017, In: F1000Research. 6, 33.

    Research output: Contribution to journal › Article › peer-review

  9. 2016

  10. Anthracene-fused isoxazolopyrrolo[2,1-a]isoquinolines via an endocyclic N-acyliminium ion cyclization: A joint experimental and theoretical study

    Ledovskaya, M. S., Molchanov, A. P., Kostikov, R. R., Panikorovsky, T. L., Gurzhiy, V. V., Ryazantsev, M. N., Boitsov, V. M. & Stepakov, A. V., 2016, In: Tetrahedron. 72, 32, p. 4827-4834 8 p.

    Research output: Contribution to journal › Article › peer-review

  11. 2015

  12. A crossed molecular beam and ab initio study on the formation of 5-and 6-methyl-1, 4-dihydronaphthalene (C 11 H 12) via the reaction of meta-tolyl (C 7 H 7) with 1, 3-butadiene (C 4 H 6)

    Muzangwa, L. G., Yang, T., Parker, D. SN., Kaiser, R. I., Mebel, A. M., Jamal, A., Ryazantsev, M. & Morokuma, K., 2015, In: Physical Chemistry Chemical Physics. 17, 12, p. 7699-7706

    Research output: Contribution to journal › Article

  13. Global investigation of potential energy surfaces for the pyrolysis of C1–C3 hydrocarbons: toward the development of detailed kinetic models from first principles

    Ryazantsev, M. N., Jamal, A., Maedab, S. & Morokuma, K., 2015, In: Physical Chemistry Chemical Physics. 17, 41, p. 27789-27805

    Research output: Contribution to journal › Article › peer-review

  14. 2014

  15. An Experimental and Theoretical Study on the Formation of 2-Methylnaphthalene (C11H10/C11H3D7) in the Reactions of the Para-Tolyl (C7H7) and Para-Tolyl-d7 (C7D7) with Vinylacetylene (C4H4)

    Parker, D. SN., Dangi, B. B., Kaiser, R. I., Jamal, A., Ryazantsev, M. N., Morokuma, K., Korte, A. & Sander, W., 2014, In: Journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment & general theory. 118, 15, p. 2709-2718

    Research output: Contribution to journal › Article › peer-review

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