Full-text resources of PSJD and other databases are now available in the new Library of Science.
Visit https://bibliotekanauki.pl

PL EN


Preferences help
enabled [disable] Abstract
Number of results
2017 | 132 | 4 | 1294-1300

Article title

Microwave Assisted Fast Synthesis of CuO Nanoflakes: Catalytic Application in the Synthesis of 1,4-Dihydropyridine

Content

Title variants

Languages of publication

EN

Abstracts

EN
CuO nanoflakes were successfully synthesized by microwave irradiation, using copper(II) sulphate and sodium hydroxide (NaOH) as the starting materials and ethanol as the solvent. The CuO nanoflakes were characterized by using techniques such as X-ray powder diffraction, field emission scanning electron microscopy, and UV-visible absorption spectroscopy, Fourier transform infra-red spectroscopy. The synthesized CuO nanoflakes were found to have morphology like nanoflakes with narrow size distribution and high purity. Moreover, the synthesized CuO nanoflakes were used as an efficient catalyst for synthesis of a series of dihydropyridine derivatives. Optimization studies with different catalysts and solvents reveal that CuO nanoparticle in the water/ethanol mixture is efficient catalyst/solvent system for the synthesis of dihydropyridine derivative.

Year

Volume

132

Issue

4

Pages

1294-1300

Physical description

Dates

published
2017-10
received
2016-10-13
(unknown)
2017-04-12

Contributors

author
  • Department of Chemistry, Jankidevi Bajaj College of Science, Jamnalal Bajaj Marg, Civil Lines, Wardha-442001, India
author
  • Department of Chemistry, Jankidevi Bajaj College of Science, Jamnalal Bajaj Marg, Civil Lines, Wardha-442001, India
author
  • Department of Physics, Jankidevi Bajaj College of Science, Jamnalal Bajaj Marg, Civil Lines, Wardha-442001, India
author
  • Department of Chemistry, Jankidevi Bajaj College of Science, Jamnalal Bajaj Marg, Civil Lines, Wardha-442001, India

References

  • [1] M.B. Gawande, R. Luque, R. Zboril, ChemCatChem 6, 3312 (2014), doi: 10.1002/cctc.201402663
  • [2] M.B. Gawande, P.S. Brancoa, R.S. Varma, Chem. Soc. Rev. 42, 3371 (2013), doi: 10.1039/C3CS35480F
  • [3] D. Wang, D. Astruc, Chem. Rev. 114, 6949 (2014), doi: 10.1021/cr500134h
  • [4] Q.M. Kainz, R. Linhardt, R.N. Grass, Adv. Funct. Mater. 24, 2020 (2014), doi: 10.1002/adfm.201303277
  • [5] S.N. Shelke, S.R. Bankar, G.R. Mhaske, S.S. Kadam, D.K. Murade, ACS Sustain. Catal. Eng. 2, 1699 (2014), doi: 10.1021/sc500160f
  • [6] S. Sá, M.B. Gawande, A. Velhinho, J.P. Veiga, N. Bundaleski, Green Chem. 16, 3494 (2014), doi: 10.1039/C4GC00558A
  • [7] M.B. Gawande, I. Rathi, D. Nogueira, Green Chem. 15, 1895 (2013), doi: 10.1039/C3GC40457A
  • [8] M. Shokouhimehr, Y. Piao, J. Kim, Y. Jang, T. Hyeon, Angew. Chem. Int. Ed. 46, 7039 (2007), doi: 10.1002/anie.200702386
  • [9] F. Shirini, M. Abedini, J. Nanosci. Nanotechnol. 13, 4838 (2013), doi: 10.1166/jnn.2013.7571
  • [10] H. Montazeri, A. Amani, H.R. Shahverdi, E. Haratifar, A.R. Shahverdi, J. Nanostruct Chem. 3, 25 (2013), doi: 10.1186/2193-8865-3-25
  • [11] P. Arumugam, P.T. Perumal, Ind. J. Chem. Sect. B Org. Incl. Med. 47, 1084 (2008)
  • [12] A.W. Bauer, W.M.M. Kirby, J.C.T. Sherris, M. Turck, Am. J. Clin. Pathol. 45, 493 (1966)
  • [13] R.A. Janis, D.J. Triggle, J. Med. Chem. 26, 775 (1983), doi: 10.1021/jm00360a001
  • [14] R.H. Boecker, F.P. Guengerich, J. Med. Chem. 29, 1596 (1986), doi: 10.1021/jm00159a007
  • [15] M.F. Gordeev, D.V. Patel, E.M. Gordon, J. Org. Chem. 61, 924 (1996), doi: 10.1021/jo951706s
  • [16] C.E. Sunkel, M. Fau de Casa-Juana, L. Santos, A.G. Garcia, C.R. Artalejo, M. Villarroya, J. Cillero, J. Med. Chem. 35, 2407 (1992), doi: 10.1021/jm00091a008
  • [17] D. Vo, W.C. Matowe, M. Ramesh, N. Iqbal, M.W. Wolowyk, S.E. Howlett, E.E. Knaus, J. Med. Chem. 38, 2851 (1995), doi: 10.1021/jm00015a007
  • [18] S.A. Sadeek, W.A. Zordok, M.S. El-Attar, M.S. Ibrahim, Bull. Chem. Soc. Ethiopia 29, 75 (2015), doi: 10.4314/bcse.v29i1.7
  • [19] Z. Luo, F. He, J. Luo, W. Zhang, Am. J. Life Sci. 3, 1 (2015), doi: 10.11648/j.ajls.s.2015030102.15
  • [20] V. Klusa, Drugs Fut. 20, 135 (1995)
  • [21] T. Godfraind, R. Miller, M. Wibo, Pharmacol. Rev. 38, 321 (1986)
  • [22] A. Sausins, G. Duburs, Heterocycles 27, 269 (1988), doi: 10.3987/REV-87-370
  • [23] A.C. Gaudio, A. Korolkovas, Y. Takahata, J. Pharm. Sci. 83, 1110 (1994), doi: 10.1002/jps.2600830809
  • [24] K. Cooper, M.J. Fray, M.J. Parry, K. Richardson, J. Steele, J. Med. Chem. 35, 3115 (1992), doi: 10.1021/jm00095a005
  • [25] A. Agarwal, P.M.S. Chauhan, Tetrahedron Lett. 46, 1345 (2005), doi: 10.1016/j.tetlet.2004.12.109
  • [26] L. Ohberg, J. Westman, Synlett 8, 1296 (2001), doi: 10.1055/s-2001-16043
  • [27] J.G. Breitenbucher, G. Figliozzi, Tetrahedron Lett. 41, 4311 (2000), doi: 10.1016/S0040-4039(00)00660-2
  • [28] J.C. Liang, J.L. Yeh, C.S. Wang, S.F. Liou, C.H. Tasi, I. Chen, J. Bioorg. Med. Chem. Lett. 10, 719 (2002), doi: 10.1016/S0960-894X(00)00087-1
  • [29] R. Miri, H. Niknahad, G. Vesal, A. Shafiee, Farmaco 57, 123 (2002), doi: 10.1016/S0014-827X(01)01183-1
  • [30] A. Dondoni, A. Massi, E. Minghini, S. Sabbatini, V. Bertoasi, J. Org. Chem. 68, 6172 (2002)
  • [31] A. Dondoni, A. Massi, E. Minghini, V. Bertoasi, Tetrahedron 60, 2311 (2004), doi: 10.1016/j.tet.2004.01.011
  • [32] S.J. Ji, Z.Q. Jiang, J. Lu, T.P. Loh, Synlett 5, 831 (2004), doi: 10.1055/s-2004-820035
  • [33] M. Maheswara, V. Siddaiah, G.L. Damu, C. Venkata Rao, Arkivoc 2, 201 (2006)
  • [34] M.A. Chari, K. Syamasundar, Catal. Commun. 6, 624 (2005), doi: 10.1016/j.catcom.2005.03.010
  • [35] S. Ko, M.N.V. Sastry, C. Lin, C.F. Yao, Tetrahedron Lett. 46, 5771 (2005), doi: 10.1016/j.tetlet.2005.05.148
  • [36] A. Kumar, R.A. Maurya, Tetrahedron Lett. 48, 3887 (2007), doi: 10.1016/j.tetlet.2007.03.130
  • [37] L.M. Wang, J. Sheng, L. Zhang, J.W. Han, Z. Fan, H. Tian, C.T. Qian, Tetrahedron 61, 1539 (2005), doi: 10.1016/j.tet.2004.11.079
  • [38] N. Tewari, N. Dwivedi, R.P. Tripathi, Tetrahedron Lett. 45, 9011 (2004), doi: 10.1016/j.tetlet.2004.10.057
  • [39] A. Kumar, R.A. Maurya, Tetrahedron 63, 1946 (2007), doi: 10.1016/j.tet.2006.12.074
  • [40] S.R. Cherkupally, R. Mekalan, Chem. Pharm. Bull. 56, 1002 (2008), doi: 10.1248/cpb.56.1002
  • [41] H. Adibi, H.A. Samimi, M. Beygzadeh, Catal. Commun. 8, 2119 (2007), doi: 10.1016/j.catcom.2007.04.022
  • [42] G. Sabitha, G.S.K. Reddy, C.S. Reddy, J.S. Yadav, Tetrahedron Lett. 44, 4129 (2003), doi: 10.1016/S0040-4039(03)00813-X
  • [43] S.B. Sapkal, K.F. Shelke, B.B. Shingate, M.S. Shingare, Tetrahedron Lett. 50, 1754 (2009), doi: 10.1016/j.tetlet.2009.01.140
  • [44] A. Maleki, Tetrahedron 68, 7827 (2012), doi: 10.1016/j.tet.2012.07.034
  • [45] A. Maleki, Tetrahedron Lett. 54, 2055 (2013), doi: 10.1016/j.tetlet.2013.01.123
  • [46] A. Maleki, N. Ghamari, M. Kamalzare, RSC Adv. 4, 9416 (2014), doi: 10.1039/C3RA47366J
  • [47] A. Maleki, M. Kamalzare, Catal. Commun. 53, 67 (2014), doi: 10.1016/j.catcom.2014.05.004
  • [48] A. Maleki, R. Rahimi, S. Maleki, N. Hamidi, RSC Adv. 4, 29765 (2014), doi: 10.1039/C4RA04654D

Document Type

Publication order reference

Identifiers

YADDA identifier

bwmeta1.element.bwnjournal-article-appv132n4p15kz
JavaScript is turned off in your web browser. Turn it on to take full advantage of this site, then refresh the page.