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  1. Suzuki–Miyaura coupling of aryl fluorosulfates in water: a modified approach for the synthesis of novel coumarin derivatives under mild conditions

    Joy, M., Sajith, A., Santra, S., Bhattacherjee, D., Beliaev, N., Zyryanov, G., Eltsov, O., Haridas, K. & Alshammari, M., 2024, In: Journal of Taibah University for Science. 18, 1, 2347679.

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

  2. Suzuki-Miyaura coupling under microwave enhanced conditions: Synthesis of 2-(hetero)aryl benzimidazoles

    Karuvalam, R. P., Haridas, K. R., Sajith, A. M., Pakkath, R., Bhaskaran, S., Padusha, M. S. A., Bakulev, V. A. & Joy, M. N., 12 Feb 2020, In: Arkivoc. 2019, 6, p. 431-445 15 p.

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

  3. Synthesis and pharmacological study of some novel benzotriazoles containing urea

    Joy, M. N., Bakulev, V. A. & Saveliev, D., 2020, Modern Synthetic Methodologies for Creating Drugs and Functional Materials, MOSM 2019: Proceedings of the III International Conference. Zyryanov, G. V., Santra, S. & Sadieva, L. K. (eds.). American Institute of Physics Inc., 4 p. 0018030. (AIP Conference Proceedings; vol. 2280).

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

  4. Synthesis of Coumarins Coupled with Benzamides as Potent Antimicrobial Agents

    Joy, M. N., Bakulev, V. A., Bodke, Y. D. & Telkar, S., 1 Sept 2020, In: Pharmaceutical Chemistry Journal. 54, 6, p. 604-621 18 p.

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

  5. Synthesis of coumarins linked with 1,2,3-triazoles under microwave irradiation and evaluation of their antimicrobial and antioxidant activity

    Joy, M. N., Bodke, Y. D., Telkar, S. & Bakulev, V. A., 1 Jan 2020, In: Journal of the Mexican Chemical Society. 64, 1, p. 46-66 21 p.

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

  6. Synthesis of some novel piperidine fused 5-thioxo-1H-1,2,4-triazoles as potential antimicrobial and antitubercular agents

    Rishikesan, R., Karuvalam, R. P., Muthipeedika, N. J., Sajith, A. M., Eeda, K. R., Pakkath, R., Haridas, K. R., Bhaskar, V., Narasimhamurthy, K. H. & Muralidharan, A., Dec 2021, In: Journal of Chemical Sciences. 133, 1, 12 p., 3.

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

  7. Synthesis of some pharmacologically relevant coumarins linked with (hetero)aryl amides

    Udhayasurian, R., Sivakumar, K., Sajith, A. M. & Joy, M. N., 2020, Modern Synthetic Methodologies for Creating Drugs and Functional Materials, MOSM 2019: Proceedings of the III International Conference. Zyryanov, G. V., Santra, S. & Sadieva, L. K. (eds.). American Institute of Physics Inc., 5 p. 0018033. (AIP Conference Proceedings; vol. 2280).

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

  8. Synthesis, characterization and biological evaluation of some new 2-[(4-hydroxy-6-methylpyrimidin-2-yl)amino]-1-(4-substituted) ethanone derivatives

    Sukanya, S. H., Venkatesh, T., Pushpavathi, I. & Muthipeedika, N. J., 5 Jul 2024, In: Journal of Molecular Structure. 1307, 1307.

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

  9. 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

  10. 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

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