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Research Article
Portrayaland Amalgamation of Pyridine and Pyrazole Byproducts for Their Biological Actions
L PRAKASH RANJIT1
T JEEVA2
S SEETHA3
123Department of Chemistry, NMAM Institute of Technology, KARNATAKA, India.
Published Online: July-August 2021
Pages: 04-06
Cite this article
No DOIReferences
[1] N. S.El-Gohary and M. I.Shaaban, Synthesis, Antimicrobial, Antiquorum-Sensing, and Cytotoxic Activities of New
Series of Isoindoline-1,3-dione, Pyrazolo[5,1-a]-isoindole, and Pyridine Derivatives (vol 348, pg 666, 2015), Archiv
Der Pharmazie, 348(11), 2015,835-835.
[2] W. A.El-Sayed,M. A. Metwally, D. S.Nada, A. A.Mohamed and A. A. H. Abdel-Rahman, Synthesis and Antimicrobial Activity of New Substituted 5-(Pyridine-3-yl)-1,3,4-Thiadiazoles and Their Sugar Derivatives, Journal of Heterocyclic Chemistry, 50(2), 2013, 194-201.
[3] A. Z. A. Elassar, Synthesis and antimicrobial activity of new polyfunctionally substituted pyridines and their fused
derivatives, Indian Journal of Chemistry Section B-Organic Chemistry Including Medicinal Chemistry, 43(6), 2004,1314-1319.
[4] A. A.Fadda, R.Rabie, H. A.Etman and A. A. S.Fouda, 1-Naphthyl-2-cyanoacetamide in heterocyclic synthesis: synthesis
and evaluation of the antimicrobial activity of some new pyridine, pyrimidine, and naphtho[2,1-b]oxazine derivatives, Research on Chemical Intermediates, 41(10), 2015,7883-7897.
[5] D.Farbstein, A.Kozak-Blickstein andA. P. Levy, Antioxidant Vitamins and Their Use in Preventing Cardiovascular
Disease, Molecules, 15(11), 2010, 8098-8110.
[6] M. A. M.Gad-Elkareem, A. M.Abdel-Fattah, and M. A. A.Elneairy, Pyridine-2(1H)-thione in heterocyclic synthesis: synthesis and antimicrobial activity of some new thio-substituted ethyl nicotinate, thieno[2,3-b]pyridine and pyridothienopyrimidine derivatives, Journal of Sulfur Chemistry, 32(3), 2011,273-286.
[7] A. A Ghoneim, A. F.El-Farargy and S.Abdelaziz, Synthesis and Antimicrobial Activities of New S-Nucleosides of
Chromeno[2,3-B] Pyridine Derivatives and C-Nucleosides of [1,2,4]Triazolo[1,5-a]Quinoline Derivatives, Nucleosides
Nucleotides & Nucleic Acids, 33(9), 2014,583-596.
[8] D. A.Horton, G. T.Bourne and M. L.Smythe, The combinatorial synthesis of bicyclic privileged structures or
privilegedsubstructures,
Series of Isoindoline-1,3-dione, Pyrazolo[5,1-a]-isoindole, and Pyridine Derivatives (vol 348, pg 666, 2015), Archiv
Der Pharmazie, 348(11), 2015,835-835.
[2] W. A.El-Sayed,M. A. Metwally, D. S.Nada, A. A.Mohamed and A. A. H. Abdel-Rahman, Synthesis and Antimicrobial Activity of New Substituted 5-(Pyridine-3-yl)-1,3,4-Thiadiazoles and Their Sugar Derivatives, Journal of Heterocyclic Chemistry, 50(2), 2013, 194-201.
[3] A. Z. A. Elassar, Synthesis and antimicrobial activity of new polyfunctionally substituted pyridines and their fused
derivatives, Indian Journal of Chemistry Section B-Organic Chemistry Including Medicinal Chemistry, 43(6), 2004,1314-1319.
[4] A. A.Fadda, R.Rabie, H. A.Etman and A. A. S.Fouda, 1-Naphthyl-2-cyanoacetamide in heterocyclic synthesis: synthesis
and evaluation of the antimicrobial activity of some new pyridine, pyrimidine, and naphtho[2,1-b]oxazine derivatives, Research on Chemical Intermediates, 41(10), 2015,7883-7897.
[5] D.Farbstein, A.Kozak-Blickstein andA. P. Levy, Antioxidant Vitamins and Their Use in Preventing Cardiovascular
Disease, Molecules, 15(11), 2010, 8098-8110.
[6] M. A. M.Gad-Elkareem, A. M.Abdel-Fattah, and M. A. A.Elneairy, Pyridine-2(1H)-thione in heterocyclic synthesis: synthesis and antimicrobial activity of some new thio-substituted ethyl nicotinate, thieno[2,3-b]pyridine and pyridothienopyrimidine derivatives, Journal of Sulfur Chemistry, 32(3), 2011,273-286.
[7] A. A Ghoneim, A. F.El-Farargy and S.Abdelaziz, Synthesis and Antimicrobial Activities of New S-Nucleosides of
Chromeno[2,3-B] Pyridine Derivatives and C-Nucleosides of [1,2,4]Triazolo[1,5-a]Quinoline Derivatives, Nucleosides
Nucleotides & Nucleic Acids, 33(9), 2014,583-596.
[8] D. A.Horton, G. T.Bourne and M. L.Smythe, The combinatorial synthesis of bicyclic privileged structures or
privilegedsubstructures,
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