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  1. 2022

  2. Thioisomünchnones versus Acrylamides via Copper-Catalyzed Reaction of Thioamides with Diazocarbonyl Compounds

    Ilkin, V. G., Filimonov, V. O., Seliverstova, E. A., Novikov, M. S., Beryozkina, T. V., Gagarin, A. A., Belskaya, N. P., Muthipeedika, N. J., Bakulev, V. A. & Dehaen, W., 16 Sept 2022, In: Journal of Organic Chemistry. 87, 18, p. 12196-12213 18 p.

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

  3. Towards novel tacrine analogues: Pd(dppf)Cl2·CH2Cl2 catalyzed improved synthesis, in silico docking and hepatotoxicity studies

    Babu, A., Joy, M. N., Sunil, K., Sajith, A. M., Santra, S., Zyryanov, G. V., Konovalova, O. A., Butorin, I. I. & Muniraju, K., 11 Aug 2022, In: RSC Advances. 12, 35, p. 22476-22491 16 p.

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

  4. Application of NMI-TfCl-mediated amide bond formation in the synthesis of biologically relevant oxadiazole derivatives employing less basic (hetero)aryl amines

    Rajendra, M. A., Naseem, M., Joy, M. N., Sunil, K., Sajith, A. M., Howari, F., Nazzal, Y., Xavier, C., Alshammari, M. B. & Haridas, K. R., Jun 2022, In: Molecular Diversity. 26, 3, p. 1761-1767 7 p.

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

  5. An efficient RP-HPLC method for UV/mass triggered purification of bis-thiazol-2-amine derivatives

    Joy, M. N., Rathnasamy, R., Karuvalam, R. P., Sajith, A. M., Beryozkina, T. V., Thennarasu, S. & Veetil, D. P., 4 Feb 2022, Actual Problems of Organic Chemistry and Biotechnology, OCBT 2020: Proceedings of the International Scientific Conference. Bakulev, V., Kovaleva, E., Glukhareva, T., Beryozkina, T., Schafran, Y., Lyubyakina, P. & Koptyaeva, O. (eds.). American Institute of Physics Inc., 020023. (AIP Conference Proceedings; vol. 2390).

    Research output: Chapter in Book/Report/Conference proceeding › Conference contribution › peer-review

  6. Synthesis, characterization, crystal structure of 4-(4-Bromo-phenyl)-2,6-dimethyl-1,4-dihydro-pyridine-3,5-dicarboxylic acid diethyl ester: Hirshfeld surface analysis and DFT calculations

    Parthasarathi, D., Padusha, M. S. A., Suganya, S., Kumaradhas, P., Sajith, A. M. & Joy, M. N., Feb 2022, In: Egyptian Journal of Chemistry. 65, 2, p. 439-448 10 p.

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

  7. Efficient L-Proline catalyzed synthesis of some new (4-substituted-phenyl)-1,5-dihydro-2H-pyrimido[4,5-d][1,3]thiazolo[3,2a]-pyrimidine-2,4(3H)-diones bearing thiazolopyrimidine derivatives and evaluation of their pharmacological activities

    Sukanya, S. H., Venkatesh, T., Aditya Rao, S. J. & Joy, M. N., 5 Jan 2022, In: Journal of Molecular Structure. 1247, 13 p., 131324.

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

  8. Heterocyclic azides: advances in their chemistry

    Bakulev, V. A., Shafran, Y. M., Beliaev, N. A., Beryozkina, T. V., Volkova, N. N., Joy, M. N. & Fan, Z., 2022, In: Russian Chemical Reviews. 91, 7, RCR5042.

    Research output: Contribution to journal › Review article › peer-review

  9. Novel synthesis of 3-(Phenyl) (ethylamino) methyl)-4- hydroxy-2H-chromen-2-one derivatives using biogenic ZnO nanoparticles and their applications

    Kumar, G. C. A., Bodke, Y. D., Manjunatha, B., Satyanarayan, N. D., Nippu, B. N. & Muthipeedika, N. J., 2022, In: Chimica Techno Acta. 9, 1, 20229104.

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

  10. SUBSTITUTED BENZOCOUMARIN DERIVATIVES: SYNTHESIS, CHARACTERIZATION, BIOLOGICAL ACTIVITIES AND MOLECULAR DOCKING WITH ADME STUDIES

    Megna, G. V., Bodke, Y. D., Shanavaz, H. & Muthipeedika, N. J., 2022, In: Chimica Techno Acta. 9, 4, 20229419.

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

  11. УСПЕХИ ХИМИИ ГЕТЕРОЦИКЛИЧЕСКИХ АЗИДОВ

    Бакулев, В. А., Шафран, Ю. М., Беляев, Н. А., Березкина, Т. В., Волкова, Н. Н., Мутхипеедика, Н. Д. & Фан, Д-Д., 2022, In: Успехи химии. 91, 7, RCR5042.

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

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