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Vol. 26 No. 24 (2014)

Copyright (c) 2014 S. Selva Ganesan*, G. Asaithampi

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Magnesium Sulfate Promoted Efficient and Green Synthesis of Aminoalkyl, Amidoalkyl and Diarylmethane Derivatives

https://doi.org/10.14233/ajchem.2014.17618
S. Selva Ganesan*
Department of Chemistry, School of Chemical and Biotechnology, SASTRA University, Thanjavur-613 401 India *Corresponding author: E-mail: selva@biotech.sastra.edu
G. Asaithampi
Department of Chemistry, School of Chemical and Biotechnology, SASTRA University, Thanjavur-613 401 India *Corresponding author: E-mail: selva@biotech.sastra.edu

Corresponding Author(s) : S. Selva Ganesan*

Asian Journal of Chemistry, Vol. 26 No. 24 (2014)

Abstract

Under solvent-free condition, magnesium sulfate promoted the synthesis of substituted aminoalkyl naphthols, amidoalkyl naphthols and diarylmethane derivatives in excellent yield. Robust dehydrating nature and mild Lewis acidity of magnesium sulfate was exploited to carry out all the transformations.

Keywords

Green synthesis Magnesium sulfate One-pot synthesis Solvent-free synthesis Substituted naphthol.
Selva Ganesan*, S., & Asaithampi, G. (2014). Magnesium Sulfate Promoted Efficient and Green Synthesis of Aminoalkyl, Amidoalkyl and Diarylmethane Derivatives. Asian Journal of Chemistry, 26(24), 8380–8382. https://doi.org/10.14233/ajchem.2014.17618
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References
  1. N. Gyémánt, H. Engi, Z. Schelz, I. Szatmári, D. Tóth, F. Fülöp, J. Molnár and P.A.M. de Witte, Br. J. Cancer, 103, 178 (2010).
  2. W.S.I. Abou-Elmagd and A.I. Hashem, Med. Chem. Res., 22, 2005 (2013).
  3. A.P.G. Nikalje, M. Patel, Y. Ranade, R. Deshpande and D. Rajani, Der Pharm. Sin., 3, 462 (2012).
  4. D.D. Holsworth, N.A. Powell, D.M. Downing, C. Cai, W.L. Cody, J.M. Ryan, R. Ostroski, M. Jalaie, J.W. Bryant and J.J. Edmunds, Bioorg. Med. Chem., 13, 2657 (2005).
  5. X.-D. Ma, X. Zhang, H.-F. Dai, S.-Q. Yang, L.-M. Yang, S.-X. Gu, Y.-T. Zheng, Q.-Q. He and F.E. Chen, Bioorg. Med. Chem., 19, 4601 (2011).
  6. M. Wang and Y. Liang, Monatsh. Chem., 142, 153 (2011).
  7. S.R. Mistry, R.S. Joshi and K.C. Maheria, J. Chem. Sci., 123, 427 (2011).
  8. B. Karmakar and J. Banerji, Tetrahedron Lett., 52, 4957 (2011).
  9. A. Kumar, M.K. Gupta and M. Kumar, Tetrahedron Lett., 51, 1582 (2010).
  10. D.M. Pore, U.V. Desai, T.S. Thopate and P.P. Wadgaonkar, Aust. J. Chem., 60, 435 (2007).
  11. B. Karami and S. Khodabakhshi, J. Serb. Chem. Soc., 76, 1191 (2011).
  12. P.B. Kisanga and J.G. Verkade, J. Org. Chem., 64, 4298 (1999).
  13. K.C. Ashalu and J.N. Rao, J. Chem. Pharm. Res., 5, 44 (2013).
  14. (a) N. Isambert, M.M.S. Duque, J.-C. Plaquevent, Y. Génisson, J. Rodriguez and T. Constantieux, Chem. Soc. Rev., 40, 1347 (2011); (b) C. de Graaff, E. Ruijter and R.V.A. Orru, Chem. Soc. Rev., 41, 3969 (2012); (c) M.S. Singh and S. Chowdhury, RSC Adv., 2, 4547 (2012).
  15. (a) S.S. Ganesan and A. Ganesan, Tetrahedron Lett., 55, 694 (2014); (b) S.S. Ganesan, N. Rajendran, S. Sundarakumar, A. Ganesan and B. Pemiah, Synthesis, 1564 (2013).
  16. K.-W. Chi, Y.S. Ahn, K.T. Shim, T.H. Park and J.S. Ahn, Bull. Korean Chem. Soc., 20, 973 (1999).
  17. A. Khazaei, M.A. Zolfigol, A.R. Moosavi-Zare, F. Abi, A. Zare, H. Kaveh, V. Khakyzadeh, M. Kazem-Rostami, A. Parhami and H. Torabi-Monfared, Tetrahedron, 69, 212 (2013).
  18. A. Kumar, M. Kumar and M.K. Gupta, Tetrahedron Lett., 50, 7024 (2009).
  19. A. Bladé-Font and T.M. Rocabayera, J. Chem. Soc. Perkin Trans. I, 841 (1982).
  20. M. Periasamy, S. Anwar and M.N. Reddy, Indian J. Chem., 48B, 1261 (2009).
  21. F.E. Ray and W.R. Haefele, J. Am. Chem. Soc., 60, 36 (1938).
  22. C. Mukhopadhyay, S. Rana and R.J. Butcher, Synth. Commun., 42, 3077 (2012).
  23. S. Seshadri, A.L. Cherian and P.Y. Pandit, Indian J. Chem., 7, 1080 (1969).
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