Synthesis of pyrazolopyridines catalyzed by nano-CdZr4(PO4)6 as a reusable catalyst

Synthesis of pyrazolopyridines catalyzed by nano-CdZr4(PO4)6 as a reusable catalyst N N N N O O H H O O H nano-CdZr (PO ) 4 4 6 NH NH 2 2 NH NH 2 2 N NH OAc N HN N N H H Electronic supplementary material The online version of this article (doi:10.1007/s11164-016-2585-9) contains supplementary material, which is available to authorized users. & Javad Safaei-Ghomi safaei@kashanu.ac.ir Department of Organic Chemistry, Faculty of Chemistry, University of Kashan, Kashan 51167, Islamic Republic of Iran School of Chemistry, College of Science, University of Tehran, Tehran 14155-6455, Islamic Republic of Iran 123 8144 J. Safaei-Ghomi et al. Keywords Nano-CdZr (PO )  Pyrazolopyridines  Nanocatalyst 4 4 6 Multicomponent reaction Introduction Pyrazolopyridines are attractive targets in organic and medicinal chemistry owing to their potency and wide spectrum of biological activities including antioxidant, antitumor and antimicrobial [1, 2], treatment of Type 2 diabetes mellitus [3], anti- virus [4], anti-Leishmania [5], protein kinase inhibitors [6] dopaminergic properties [7] and can also serve as synthetic intermediates for many kinds of pharmaceuticals or drug precursors [8–10]. Therefore, the development of simple methods for the synthesis of pyrazolopyridines is a major challenge and an interesting field in chemistry. The synthesis of pyrazolopyridine derivatives has been reported in http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Research on Chemical Intermediates Springer Journals

Synthesis of pyrazolopyridines catalyzed by nano-CdZr4(PO4)6 as a reusable catalyst

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Publisher
Springer Netherlands
Copyright
Copyright © 2016 by Springer Science+Business Media Dordrecht
Subject
Chemistry; Catalysis; Physical Chemistry; Inorganic Chemistry
ISSN
0922-6168
eISSN
1568-5675
D.O.I.
10.1007/s11164-016-2585-9
Publisher site
See Article on Publisher Site

Abstract

N N N N O O H H O O H nano-CdZr (PO ) 4 4 6 NH NH 2 2 NH NH 2 2 N NH OAc N HN N N H H Electronic supplementary material The online version of this article (doi:10.1007/s11164-016-2585-9) contains supplementary material, which is available to authorized users. & Javad Safaei-Ghomi safaei@kashanu.ac.ir Department of Organic Chemistry, Faculty of Chemistry, University of Kashan, Kashan 51167, Islamic Republic of Iran School of Chemistry, College of Science, University of Tehran, Tehran 14155-6455, Islamic Republic of Iran 123 8144 J. Safaei-Ghomi et al. Keywords Nano-CdZr (PO )  Pyrazolopyridines  Nanocatalyst 4 4 6 Multicomponent reaction Introduction Pyrazolopyridines are attractive targets in organic and medicinal chemistry owing to their potency and wide spectrum of biological activities including antioxidant, antitumor and antimicrobial [1, 2], treatment of Type 2 diabetes mellitus [3], anti- virus [4], anti-Leishmania [5], protein kinase inhibitors [6] dopaminergic properties [7] and can also serve as synthetic intermediates for many kinds of pharmaceuticals or drug precursors [8–10]. Therefore, the development of simple methods for the synthesis of pyrazolopyridines is a major challenge and an interesting field in chemistry. The synthesis of pyrazolopyridine derivatives has been reported in

Journal

Research on Chemical IntermediatesSpringer Journals

Published: May 31, 2016

References

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