Synthesis and Evaluation of Antimicrobial Activity of Nitrones from Derivatives of Aryl-Substituted Dihydroisoquinoline

This paper describes the synthesis of a series of dihydroisoquinoline nitrones by isomerization of the corresponding oxaziridines. Nitrones 4a–c were obtained in excellent yields and high purity by a simple and effective method from the isomerization of oxaziridines. The synthesized compounds were a...

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Main Authors: Mouna Bouzid, Raed Abdennabi, Mohamed Damak, Majed Kammoun
Format: Article
Language:English
Published: Wiley 2015-01-01
Series:Journal of Chemistry
Online Access:http://dx.doi.org/10.1155/2015/803867
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author Mouna Bouzid
Raed Abdennabi
Mohamed Damak
Majed Kammoun
author_facet Mouna Bouzid
Raed Abdennabi
Mohamed Damak
Majed Kammoun
author_sort Mouna Bouzid
collection DOAJ
description This paper describes the synthesis of a series of dihydroisoquinoline nitrones by isomerization of the corresponding oxaziridines. Nitrones 4a–c were obtained in excellent yields and high purity by a simple and effective method from the isomerization of oxaziridines. The synthesized compounds were also evaluated for their antibacterial activity against Gram-positive and Gram-negative bacteria and fungus.
format Article
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institution Kabale University
issn 2090-9063
2090-9071
language English
publishDate 2015-01-01
publisher Wiley
record_format Article
series Journal of Chemistry
spelling doaj-art-51c8d725c4124167ab7054e8afa5b6b72025-02-03T05:46:05ZengWileyJournal of Chemistry2090-90632090-90712015-01-01201510.1155/2015/803867803867Synthesis and Evaluation of Antimicrobial Activity of Nitrones from Derivatives of Aryl-Substituted DihydroisoquinolineMouna Bouzid0Raed Abdennabi1Mohamed Damak2Majed Kammoun3Laboratory of Chemistry of Natural Products, Faculty of Science, Sfax University, BP 1171, 3000 Sfax, TunisiaLaboratory of Plant Biotechnology Applied to Crop Improvement, Faculty of Science, Sfax University, BP 1171, 3000 Sfax, TunisiaLaboratory of Chemistry of Natural Products, Faculty of Science, Sfax University, BP 1171, 3000 Sfax, TunisiaLaboratory of Chemistry of Natural Products, Faculty of Science, Sfax University, BP 1171, 3000 Sfax, TunisiaThis paper describes the synthesis of a series of dihydroisoquinoline nitrones by isomerization of the corresponding oxaziridines. Nitrones 4a–c were obtained in excellent yields and high purity by a simple and effective method from the isomerization of oxaziridines. The synthesized compounds were also evaluated for their antibacterial activity against Gram-positive and Gram-negative bacteria and fungus.http://dx.doi.org/10.1155/2015/803867
spellingShingle Mouna Bouzid
Raed Abdennabi
Mohamed Damak
Majed Kammoun
Synthesis and Evaluation of Antimicrobial Activity of Nitrones from Derivatives of Aryl-Substituted Dihydroisoquinoline
Journal of Chemistry
title Synthesis and Evaluation of Antimicrobial Activity of Nitrones from Derivatives of Aryl-Substituted Dihydroisoquinoline
title_full Synthesis and Evaluation of Antimicrobial Activity of Nitrones from Derivatives of Aryl-Substituted Dihydroisoquinoline
title_fullStr Synthesis and Evaluation of Antimicrobial Activity of Nitrones from Derivatives of Aryl-Substituted Dihydroisoquinoline
title_full_unstemmed Synthesis and Evaluation of Antimicrobial Activity of Nitrones from Derivatives of Aryl-Substituted Dihydroisoquinoline
title_short Synthesis and Evaluation of Antimicrobial Activity of Nitrones from Derivatives of Aryl-Substituted Dihydroisoquinoline
title_sort synthesis and evaluation of antimicrobial activity of nitrones from derivatives of aryl substituted dihydroisoquinoline
url http://dx.doi.org/10.1155/2015/803867
work_keys_str_mv AT mounabouzid synthesisandevaluationofantimicrobialactivityofnitronesfromderivativesofarylsubstituteddihydroisoquinoline
AT raedabdennabi synthesisandevaluationofantimicrobialactivityofnitronesfromderivativesofarylsubstituteddihydroisoquinoline
AT mohameddamak synthesisandevaluationofantimicrobialactivityofnitronesfromderivativesofarylsubstituteddihydroisoquinoline
AT majedkammoun synthesisandevaluationofantimicrobialactivityofnitronesfromderivativesofarylsubstituteddihydroisoquinoline