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Catalytic Synthesis of 2,3-Diphenylquinoxalines at Room Temperature Using Silica Supported Preyssler Heteropolyacid Catalysts, H14[NaP5W30O110]/SiO2

Received: 10 April 2015    Accepted: 22 April 2015    Published: 28 April 2015
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Abstract

The reaction of Preyssler heteropolyacid, which was used as a catalyst for the room temperature synthesis of quinoxaline derivatives from 1,2-diamino compounds and 1,2-dicarbonyl compounds. The catalyst could be recycled and reused several times without any loss of efficiency.

Published in American Journal of Heterocyclic Chemistry (Volume 1, Issue 1)
DOI 10.11648/j.ajhc.20150101.13
Page(s) 13-20
Creative Commons

This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited.

Copyright

Copyright © The Author(s), 2024. Published by Science Publishing Group

Keywords

Quinoxalines, 1,2-Diamino Compounds, 1,2-Dicarbonyl Compounds, Preyssler, Catalyst

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Cite This Article
  • APA Style

    Ali Gharib, Nader Noroozi Pesyan, Leila Vojdani Fard, Mina Roshani. (2015). Catalytic Synthesis of 2,3-Diphenylquinoxalines at Room Temperature Using Silica Supported Preyssler Heteropolyacid Catalysts, H14[NaP5W30O110]/SiO2. American Journal of Heterocyclic Chemistry, 1(1), 13-20. https://doi.org/10.11648/j.ajhc.20150101.13

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    ACS Style

    Ali Gharib; Nader Noroozi Pesyan; Leila Vojdani Fard; Mina Roshani. Catalytic Synthesis of 2,3-Diphenylquinoxalines at Room Temperature Using Silica Supported Preyssler Heteropolyacid Catalysts, H14[NaP5W30O110]/SiO2. Am. J. Heterocycl. Chem. 2015, 1(1), 13-20. doi: 10.11648/j.ajhc.20150101.13

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    AMA Style

    Ali Gharib, Nader Noroozi Pesyan, Leila Vojdani Fard, Mina Roshani. Catalytic Synthesis of 2,3-Diphenylquinoxalines at Room Temperature Using Silica Supported Preyssler Heteropolyacid Catalysts, H14[NaP5W30O110]/SiO2. Am J Heterocycl Chem. 2015;1(1):13-20. doi: 10.11648/j.ajhc.20150101.13

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  • @article{10.11648/j.ajhc.20150101.13,
      author = {Ali Gharib and Nader Noroozi Pesyan and Leila Vojdani Fard and Mina Roshani},
      title = {Catalytic Synthesis of 2,3-Diphenylquinoxalines at Room Temperature Using Silica Supported Preyssler Heteropolyacid Catalysts, H14[NaP5W30O110]/SiO2},
      journal = {American Journal of Heterocyclic Chemistry},
      volume = {1},
      number = {1},
      pages = {13-20},
      doi = {10.11648/j.ajhc.20150101.13},
      url = {https://doi.org/10.11648/j.ajhc.20150101.13},
      eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.ajhc.20150101.13},
      abstract = {The reaction of Preyssler heteropolyacid, which was used as a catalyst for the room temperature synthesis of quinoxaline derivatives from 1,2-diamino compounds and 1,2-dicarbonyl compounds. The catalyst could be recycled and reused several times without any loss of efficiency.},
     year = {2015}
    }
    

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    T1  - Catalytic Synthesis of 2,3-Diphenylquinoxalines at Room Temperature Using Silica Supported Preyssler Heteropolyacid Catalysts, H14[NaP5W30O110]/SiO2
    AU  - Ali Gharib
    AU  - Nader Noroozi Pesyan
    AU  - Leila Vojdani Fard
    AU  - Mina Roshani
    Y1  - 2015/04/28
    PY  - 2015
    N1  - https://doi.org/10.11648/j.ajhc.20150101.13
    DO  - 10.11648/j.ajhc.20150101.13
    T2  - American Journal of Heterocyclic Chemistry
    JF  - American Journal of Heterocyclic Chemistry
    JO  - American Journal of Heterocyclic Chemistry
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    PB  - Science Publishing Group
    SN  - 2575-5722
    UR  - https://doi.org/10.11648/j.ajhc.20150101.13
    AB  - The reaction of Preyssler heteropolyacid, which was used as a catalyst for the room temperature synthesis of quinoxaline derivatives from 1,2-diamino compounds and 1,2-dicarbonyl compounds. The catalyst could be recycled and reused several times without any loss of efficiency.
    VL  - 1
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Author Information
  • Department of Chemistry, Islamic Azad University, Mashhad, Iran; Department of Chemistry, Agricultural Researches and Services Center, Mashhad, Iran

  • Department of Chemistry, Faculty of Science, Urmia University, Urmia, Iran

  • Education Ministry, Education Organization of Razavi Khorasan, Mashhad, Iran

  • Department of Chemistry, Islamic Azad University, Mashhad, Iran

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