Ugi, I., 2001. Recent progress in the chemistry of multicomponent reactions. Pure and Applied Chemistry, 73(1), pp.187-191.
Climent, M.J., Corma, A. and Iborra, S., 2012. Homogeneous and heterogeneous catalysts for multicomponent reactions. RSC advances, 2(1), pp.16-58.
Stercker, A.Libeigs Ann. Chem. 1882,215,1.
Bhaskar, G., Arun, Y., Balachandran, C., Saikumar, C. and Perumal, P.T., 2012. Synthesis of novel spirooxindole derivatives by one pot multicomponent reaction and their antimicrobial activity. European journal of medicinal chemistry, 51, pp.79-91.
Dömling, A. and Ugi, I., 2000. Multicomponent reactions with isocyanides. Angewandte Chemie International Edition, 39(18), pp.3168-3210.
Allahresani, A., Taheri, B. and Nasseri, M.A., 2018. Synthesis of spirooxindole derivatives catalyzed by GN/SO 3 H nanocomposite as a heterogeneous solid acid. Research on Chemical Intermediates, 44(11), pp.6979-6993.
Bhaskar, G., Arun, Y., Balachandran, C., Saikumar, C. and Perumal, P.T., 2012. Synthesis of novel spirooxindole derivatives by one pot multicomponent reaction and their antimicrobial activity. European journal of medicinal chemistry, 51, pp.79-91.
Shanthi, G., Subbulakshmi, G. and Perumal, P.T., 2007. A new InCl3-catalyzed, facile and efficient method for the synthesis of spirooxindoles under conventional and solvent-free microwave conditions. Tetrahedron, 63(9), pp.2057-2063.
Hassani, H., Zakerinasab, B. and Nozarie, A., 2018. Sulfonic acid supported on Fe2O3/VO2 nanocatalyst: a highly efficient and reusable nanocatalyst for synthesis of spirooxindole derivatives. Asian Journal of Green Chemistry, 2(1), pp.59-69.
Hemmat, K., Nasseri, M.A. and Allahresani, A., 2019. CoFe2O4@ SiO2@ Co (III) Salen Complex: A Magnetically Recyclable Heterogeneous Catalyst for the Synthesis of Quinoline Derivatives in Water. ChemistrySelect, 4(14), pp.4339-4346.
Allahresani, A., Taheri, B. and Nasseri, M.A., 2018. A green synthesis of spirooxindole derivatives catalyzed by SiO 2@ gC 3 N 4 nanocomposite. Research on Chemical Intermediates, 44(2), pp.1173-1188.
Yu, F., Huang, R., Ni, H., Fan, J., Yan, S. and Lin, J., 2013. Three-component stereoselective synthesis of spirooxindole derivatives. Green chemistry, 15(2), pp.453-462.
Nandakumar, A., Thirumurugan, P., Perumal, P.T., Vembu, P., Ponnuswamy, M.N. and Ramesh, P., 2010. One-pot multicomponent synthesis and anti-microbial evaluation of 2′-(indol-3-yl)-2-oxospiro (indoline-3, 4′-pyran) derivatives. Bioorganic & medicinal chemistry letters, 20(14), pp.4252-4258.
Thangamani, A., 2010. Regiospecific synthesis and biological evaluation of spirooxindolopyrrolizidines via [3+ 2] cycloaddition of azomethine ylide. European journal of medicinal chemistry, 45(12), pp.6120-6126.
Yeung, B.K., Zou, B., Rottmann, M., Lakshminarayana, S.B., Ang, S.H., Leong, S.Y., Tan, J., Wong, J., Keller-Maerki, S., Fischli, C. and Goh, A., 2010. Spirotetrahydro β-carbolines (spiroindolones): a new class of potent and orally efficacious compounds for the treatment of malaria. Journal of medicinal chemistry, 53(14), pp.5155-5164.
Ghahremanzadeh, R., Rashid, Z., Zarnani, A.H. and Naeimi, H., 2013. Synthesis of novel spirooxindoles in water by using MnFe2O4 nanoparticles as an efficient magnetically recoverable and reusable catalyst. Applied Catalysis A: General, 467, pp.270-278.
KL, J.T.K., 2006. Wolff K. Yin H. Bieza K. Caldwell J. Bursulaya B. Wu TY.-H. He Y. Bioorg. Med. Chem. Lett, 16, p.2105.

Engineering and Technology Quarterly Reviews

ISSN 2622-9374

Vol.3 No.2 (2020)

The Asian Institute of Research

Engineering and Technology Quarterly Reviews

Vol.3, No.2, December 2020 (E-Version First)

Journal of Social and Political Sciences

Journal of Economics and Business

Education Quarterly Reviews

Journal of Health and Medical Sciences

Engineering and Technology Quarterly Reviews

About Us

Stay Connected

Contact Us