MICROWAVE-ASSISTED ONE-POT SYNTHESIS OF SOME NEW FLAVONOLS BY MODIFIED ALGAR–FLYNN–OYAMADA REACTION AND THEIR ANTIMICROBIAL ACTIVITY

Authors

  • Ashok Dongamanti Department of Chemistry, Osmania University
  • Ahmed Kifah Mohsin Department of Chemistry, Osmania University
  • Vijaya Lakshmi Bommidi Department of Chemistry, Osmania University
  • Sarasija Madderla Department of Chemistry, Satavahana University
  • Adam Shaik Regional Agricultural Research Station, ANGRAU

DOI:

https://doi.org/10.1007/3049

Keywords:

3-hydroxy-2-[1-phenyl-3-(thiophen-2-yl)-1H-pyrazol-4-yl]-4H-chromen-4-ones, 1-phenyl-3-(thiophen-2-yl)-1H-pyrazole-4-carbaldehyde, antimicrobial activity, microwave irradiation, modified Algar–Flynn–Oyamada reaction

Abstract

A new series of 3-hydroxy-2-[1-phenyl-3-(thiophen-2-yl)-1H-pyrazol-4-yl]-4H-chromen-4-ones has been synthesized from substituted 2-hydroxyacetophenones and 1-phenyl-3-(thiophen-2-yl)-1H-pyrazole-4-carbaldehyde using NaOH and H2O2 by modified Algar–Flynn–Oyamada reaction under conventional and microwave irradiation conditions. In this method flavonols are synthesized without isolating chalcones in good yields (80–85%). The structures of the compounds were established on the basis of IR, 1H, 13C NMR and mass spectral and elemental analysis data. The synthesized compounds were screened for their antibacterial and antifungal activities.

How to Cite
Ashok, D.; Kifah, M. A.; Vijaya Lakshmi, B.; Sarasija, M.; Adam, S. Chem. Heterocycl. Compd. 2016, 52, 172. [Khim. Geterotsikl. Soedin. 2016, 52, 172.]

For this article in the English edition see DOI 10.1007/s10593-016-1852-4

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Published

2016-03-15

Issue

Vol. 52 No. 3 (2016)

Section

Original Papers