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Synthesis and antimicrobial activity of novel quinazolinone–thiazolidine–quinoline compounds

A series of 2-(2-chloroquinolin-3-yl)-5-((aryl)benzylidene)-3-(4-oxo-2-phenylquinazolin-3(4H)-yl)thiazolidin-4-ones (V)(1–12) have been synthesized. In order to establish optimization of different parameters of chemical transformation, that is the reaction pathway for each step and reaction conditio...

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Detalles Bibliográficos
Autores principales: Desai, N.C., Dodiya, Amit, Shihory, Niraj
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Production and hosting by Elsevier B.V. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7148931/
http://dx.doi.org/10.1016/j.jscs.2011.04.001
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author Desai, N.C.
Dodiya, Amit
Shihory, Niraj
author_facet Desai, N.C.
Dodiya, Amit
Shihory, Niraj
author_sort Desai, N.C.
collection PubMed
description A series of 2-(2-chloroquinolin-3-yl)-5-((aryl)benzylidene)-3-(4-oxo-2-phenylquinazolin-3(4H)-yl)thiazolidin-4-ones (V)(1–12) have been synthesized. In order to establish optimization of different parameters of chemical transformation, that is the reaction pathway for each step and reaction conditions in the each step, in the present paper, different solvents and catalysts were used. The structures of the synthesized compounds were assigned on the basis of elemental analysis, IR, (1)H NMR and (13)C NMR spectral data. All the newly synthesized compounds were screened against various strains of bacteria and fungi.
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spelling pubmed-71489312020-04-13 Synthesis and antimicrobial activity of novel quinazolinone–thiazolidine–quinoline compounds Desai, N.C. Dodiya, Amit Shihory, Niraj Journal of Saudi Chemical Society Original Article A series of 2-(2-chloroquinolin-3-yl)-5-((aryl)benzylidene)-3-(4-oxo-2-phenylquinazolin-3(4H)-yl)thiazolidin-4-ones (V)(1–12) have been synthesized. In order to establish optimization of different parameters of chemical transformation, that is the reaction pathway for each step and reaction conditions in the each step, in the present paper, different solvents and catalysts were used. The structures of the synthesized compounds were assigned on the basis of elemental analysis, IR, (1)H NMR and (13)C NMR spectral data. All the newly synthesized compounds were screened against various strains of bacteria and fungi. Production and hosting by Elsevier B.V. 2013-07 2011-04-12 /pmc/articles/PMC7148931/ http://dx.doi.org/10.1016/j.jscs.2011.04.001 Text en Copyright © 2011 Production and hosting by Elsevier B.V. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Original Article
Desai, N.C.
Dodiya, Amit
Shihory, Niraj
Synthesis and antimicrobial activity of novel quinazolinone–thiazolidine–quinoline compounds
title Synthesis and antimicrobial activity of novel quinazolinone–thiazolidine–quinoline compounds
title_full Synthesis and antimicrobial activity of novel quinazolinone–thiazolidine–quinoline compounds
title_fullStr Synthesis and antimicrobial activity of novel quinazolinone–thiazolidine–quinoline compounds
title_full_unstemmed Synthesis and antimicrobial activity of novel quinazolinone–thiazolidine–quinoline compounds
title_short Synthesis and antimicrobial activity of novel quinazolinone–thiazolidine–quinoline compounds
title_sort synthesis and antimicrobial activity of novel quinazolinone–thiazolidine–quinoline compounds
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7148931/
http://dx.doi.org/10.1016/j.jscs.2011.04.001
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