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Synthesis of Quinoline Derivatives Using Double Perovskite Bi1.97Eu0.03MoO6 Heterogeneous Nanocatalyst

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Abstract

Double perovskite Bi1.97Eu0.03MoO6 was synthesized and used to catalyze the synthesis of quinoline derivatives from aliphatic ketones and 2-aminoaryl ketones at room temperature. The catalyst showed excellent activity and stability, and it could be reused at least six times without significant loss of activity.

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REFERENCES

  1. Michael, J.P., Nat. Prod. Rep., 2007, vol. 24, p. 223. https://doi.org/10.1039/B509528J

    Article  CAS  PubMed  Google Scholar 

  2. Thatcher, T.H., Luzina, I., Fishelevich, R., Tomai, M.A., Miller, R.L., and Gaspari, A.A., J. Invest. Dermatol., 2006, vol. 126, p. 821. https://doi.org/10.1038/sj.jid.5700167

    Article  CAS  PubMed  Google Scholar 

  3. Klingenstein, R., Melnyk, P., Leliveld, S.R., Rycke­busch, A., and Korth, C., J. Med. Chem., 2006, vol. 49, p. 5300. https://doi.org/10.1021/jm0602763

    Article  CAS  PubMed  Google Scholar 

  4. Narender, P., Srinivas, U., Ravinder, M., Rao, B.A., Ramesh, C., Harakishore, K., Gangadasu, B., Murthy, U.S.N., and Rao, V.J., Bioorg. Med. Chem., 2006, vol. 14, p. 4600. https://doi.org/10.1016/j.bmc.2006.02.020

    Article  CAS  PubMed  Google Scholar 

  5. Pellerano, I., Savini, L., Massarelli, P., Bruni, G., and Fiaschi, A.I., Farmaco, 1990, vol. 45, p. 269. PMID: 2383343

    CAS  PubMed  Google Scholar 

  6. Agui, H., Mitani, T., Izawa, A., Komatsu, T., Naka­gome, T., J. Med. Chem., 1977, vol. 20, p. 791. https://doi.org/10.1021/jm00216a010

    Article  CAS  PubMed  Google Scholar 

  7. Sopková-de Oliveira Santos, P., Verhaeghe, P., Lohier, J.-F., Rathelot, P., Vanelle, P., and Rault, S., Acta Crystallogr., Sect. C, 2007, vol. 63, p. o643. https://doi.org/10.1107/S0108270107046550

  8. Marella, A., Tanwar, O.P., Saha, R., Ali, M.R., Srivastava, S., Akhter, M., Shaquiquzzaman, M., and Alam, M.M., Saudi Pharm. J., 2013, vol. 21, p. 1. https://doi.org/10.1016/j.jsps.2012.03.002

    Article  PubMed  Google Scholar 

  9. Babu, M.S., Kamble, R.R., Hoskeri, J., Prasad, J., and Gangadhar, Y., Med. Chem. Res., 2014, vol. 23, p. 2727. https://doi.org/10.1007/s00044-013-0855-2

    Article  CAS  Google Scholar 

  10. Gabriele, B., Mancuso, R., Salerno, G., Ruffolo, G., and Plastina, P., J. Org. Chem., 2007, vol. 72, p. 6873. https://doi.org/10.1021/jo071094z

    Article  CAS  PubMed  Google Scholar 

  11. Francis, V., Mierde, H.V., Voort, P.V., and Vos, D.D., Eur. J. Org. Chem., 2008, vol. 2008, p. 1625. https://doi.org/10.1002/ejoc.200701001

    Article  Google Scholar 

  12. Yuan, L.X., Ding, P., Sheng, H.J., and Ming, C.C., Org. Lett., 2007, vol. 9, p. 2645. https://doi.org/10.1021/ol701581g

    Article  CAS  Google Scholar 

  13. Muscia, G.C., Bollini, M., Carnevale, J.P., Bruno, A.M., and Asis, S.E., Tetrahedron Lett., 2006, vol. 47, p. 8811. https://doi.org/10.1016/j.tetlet.2006.10.073

    Article  CAS  Google Scholar 

  14. Hu, Y.Z., Zhang, G., and Thummel, R.P., Org. Lett., 2003, vol. 5, p. 2251. https://doi.org/10.1021/ol034559q

    Article  CAS  PubMed  Google Scholar 

  15. Jiang, B., Dong, J.J., Jin, Y., Long Du, X., and Xu, M., Eur. J. Org. Chem., 2008, vol. 2008, p. 2693. https://doi.org/10.1002/ejoc.200800121

    Article  CAS  Google Scholar 

  16. Wu, J., Xia, H.G., and Gao, K., Org. Biomol. Chem., 2006, vol. 4, p. 126. https://doi.org/10.1039/B606717D

    Article  CAS  PubMed  Google Scholar 

  17. Dabiri, M., Salehi, P., Mostafa, B., and Nikcheg, M.S., Tetrahedron Lett., 2008, vol. 49, p. 5366. https://doi.org/10.1016/j.tetlet.2008.06.054

    Article  CAS  Google Scholar 

  18. Tejeswararao, D., Asian J. Chem., 2016, vol. 28, p. 2353. https://doi.org/10.14233/ajchem.2016.19533

    Article  CAS  Google Scholar 

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ACKNOWLEDGMENTS

The authors thank the GMR Institute of Technology, Rajam, for support of this work.

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Authors and Affiliations

  1. Department of Chemistry, GMR Institute of Technology, 532127, Rajam, Andhra Pradesh, India

    D. Tejeswara Rao

  2. Department of Chemistry, Lendi Institute of Engineering and Technology, Jonnada, 535005, Vizianagaram, Andhra Pradesh, India

    P. Seetharam

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  1. D. Tejeswara Rao
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  2. P. Seetharam
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Correspondence to D. Tejeswara Rao.

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Rao, D.T., Seetharam, P. Synthesis of Quinoline Derivatives Using Double Perovskite Bi1.97Eu0.03MoO6 Heterogeneous Nanocatalyst. Russ J Org Chem 58, 1042–1047 (2022). https://doi.org/10.1134/S1070428022070156

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