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Green Processing and Synthesis

Editor-in-Chief: Hessel, Volker

Editorial Board: Akay, Galip / Arends, Isabel / Cann, Michael C. / Cheng, Yi / Cravotto, Giancarlo / Gruber-Wölfler, Heidrun / Kralisch, Dana / D. P. Nigam, Krishna / Saha, Basudeb / Serra, Christophe A. / Zhang, Wei

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Volume 5, Issue 3

Issues

Green chemistry preparation of MgO grit like nanostructures: efficient catalyst for the synthesis of 4H-pyrans and α,α′-bis(substituted-benzylidene) cycloalkanone derivatives

Akbar Mobinikhaledi / Atisa Yazdanipour / Majid Ghashang
  • Department of Chemistry, Faculty of Science, Najafabad Branch, Islamic Azad University, Najafabad, Esfahan, Iran
  • Other articles by this author:
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Published Online: 2016-05-31 | DOI: https://doi.org/10.1515/gps-2015-0136

Abstract

A grit like nanostructure of MgO was prepared in a medium of mulberry leaves extract and characterized on the basis of field emission scanning electronic microscopy (FE-SEM), X-ray diffraction (XRD), and energy dispersive X-ray (EDX) analysis. It was found to be an efficient catalyst for one-pot synthesis of 4H-pyrans from the reaction of malononitrile and α,α′-bis(substituted-benzylidene) cycloalkanones in good to high yields.

Keywords: 4H-pyrans; cycloalkanones; green; mulberry leaves; nanoparticles

References

  • [1]

    Morgan LR, Jursic BS, Hooper CL, Neumann DM, Thangaraj K, LeBlanc B. Bioorg. Med. Chem. Lett. 2002, 12, 3407–3411.Google Scholar

  • [2]

    Moon DO, Kim K-C, Jin CY, Han MH, Park C, Lee KJ, Park YM, Choi YH, Kim GY. Int. Immunopharmacol. 2007, 7, 222–229.Google Scholar

  • [3]

    Wu J YC, Fong WF, Zhang JX, Leung CH, Kwong HL, Yang MS, Li D, Cheung HY. Eur. J. Pharmacol. 2003, 473, 9–17.Google Scholar

  • [4]

    Kemnitzer W, Drewe J, Jiang S, Zhang H, Zhao J, Crogan-Grundy C, Xu L, Lamothe S, Gourdeau H, Denis R, Tseng B, Kasibhatla S, Cai SX. J. Med. Chem. 2007, 50, 2858–2864.Google Scholar

  • [5]

    Raj T, Bhatia RK, Sharma M, Saxena A, Ishar M. Eur. J. Med. Chem. 2010, 45, 790–794.Google Scholar

  • [6]

    Flavin MT, Rizzo JD, Khilevich A, Kucherenko A, Sheinkman AK, Vilaychack V, Lin L, Chen W, Greenwood EM, Pengsuparp T. J. Med. Chem. 1996, 39, 1303–1313.Google Scholar

  • [7]

    Jensen AA, Erichsen MN, Nielsen CW, Stensbøl TB, Kehler J, Bunch L. J. Med. Chem. 2009, 52, 912–915.Google Scholar

  • [8]

    Urbahns K, Horváth E, Stasch JNP, Mauler F. Bioorg. Med. Chem. Lett. 2003, 13, 2637–2639.Google Scholar

  • [9]

    O’Callaghan CN, McMurry TBH, O’Brien JE. J. Chem. Soc., Perkin Trans. 1. 1995, 417–420.Google Scholar

  • [10]

    Lei M, Ma L, Hu L. Tetrahedron Lett. 2011, 52, 2597–2600.Google Scholar

  • [11]

    Quintela J, Peinador C, Moreira MJ. Tetrahedron 1995, 51, 5901–5912.Google Scholar

  • [12]

    Srivastava S, Batra S, Bhaduri A. Indian J. Chem. Sect. B: Org. Chem. Incl. Med. 1996, 35, 602–604.Google Scholar

  • [13]

    Seifi M, Sheibani H. Catal. Lett. 2008, 126, 275–279.Google Scholar

  • [14]

    Mahdavinia GH, Bigdeli MA, Kooti F. Bull. Chem. Soc. Ethiop. 2012, 26, 249–255.Google Scholar

  • [15]

    Karimi-Jaberi Z, Pooladian B. Scientific World J. 2012, doi: .CrossrefGoogle Scholar

  • [16]

    Wang XS, Yang GS, Zhao G. Tetrahedron: Asymmetry 2008, 19, 709–714.Web of ScienceGoogle Scholar

  • [17]

    Mobinikhaledi A, Foroughifar N, Moghanian H, Keshavarzi N. J. Saudi Chem. Soc. 2015, 19, 399–403.Google Scholar

  • [18]

    Wang LM, Shao JH, Tian H, Wang YH, Liu B. J. Fluorine Chem. 2006, 127, 97–100.Google Scholar

  • [19]

    Valizadeh H, Azimi A. JICS. 2011, 8, 123–130.Google Scholar

  • [20]

    Zhang SG, Yin SF, Wei YD, Luo SL, Au CT. Catal. Lett. 2012, 142, 608–614.Google Scholar

  • [21]

    Foroughifar N, Mobinikhaledi A, Moghanian H. Chem. Lett. 2010, 39, 180–181.Google Scholar

  • [22]

    Foroughifar N, Mobinikhaledi A, Moghanian H. Synth. Commun. 2009, 39, 3668–3676.Google Scholar

  • [23]

    Mobinikhaledi A, Yazdanipour A, Ghashang M. Turk J Chem. 2015, 39, 667–675.Google Scholar

  • [24]

    Brahmachari G, Laskar S. Phosphorus Sulfur Silicon Relat. Elem. 2014, 189, 873–888.Google Scholar

  • [25]

    Mohammadzadeh I, Sheibani H. Chin. Chem. Lett. 2012, 23, 1327–1330.Google Scholar

About the article

Akbar Mobinikhaledi

Akbar Mobinikhaledi: 1986 BSc (Chemistry), Isfahan University, Iran; 1991 MSc (Organic Chemistry), University of Mazandaran, Iran; 1998 PhD, University of Otago, New Zealand. Currently, he is a professor of Organic Chemistry at the Chemistry Department, University of Arak, Arak, Iran. His research areas are organic synthesis, catalyst, nanochemistry and organometallics. He has published 154 papers.

Atisa Yazdanipour

Atisa Yazdanipour is currently a PhD student in organic chemistry at the Department of Chemistry, Arak University, under the direction of Professor Akbar Mobinikhaledi. She received her BSc in pure chemistry at the National University of Iran (Shahid Beheshti University, SBU, Tehran, Iran) in 2000. She got her MSc under the direction of Professor Peiman Salehi and Professor Mohammad Mehdi Khodaei at Razi University in 2003. Her field of interest is the green synthesis of new nanostructured metal oxides, and their applications in multicomponent reactions (MCRs).

Majid Ghashang

Majid Ghashang completed his PhD at Sistan and Baluchestan University of Chemistry in 2011. He is a faculty member of the Department of Chemistry of Najafabad Branch, Islamic Azad University. He has published more than 111 papers in reputed journals and has been serving as an editorial board member of various journals. His main areas of interest are organic chemistry, catalysis, nano-materials and statistical design.


Received: 2016-01-18

Accepted: 2016-04-04

Published Online: 2016-05-31

Published in Print: 2016-06-01


Citation Information: Green Processing and Synthesis, Volume 5, Issue 3, Pages 289–295, ISSN (Online) 2191-9550, ISSN (Print) 2191-9542, DOI: https://doi.org/10.1515/gps-2015-0136.

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