Cargando…
Synthesis of Functionalized Arylaziridines as Potential Antimicrobial Agents
By using the Suzuki-Miyaura protocol, a simple straightforward synthesis of functionalized 2-arylaziridines has been developed. By means of this synthetic strategy from readily available ortho-, meta- and para-bromophenylaziridines and aryl- or heteroarylboronic acids, new aziridines could be obtain...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271868/ https://www.ncbi.nlm.nih.gov/pubmed/25093988 http://dx.doi.org/10.3390/molecules190811505 |
_version_ | 1783377026528313344 |
---|---|
author | Giovine, Arianna Muraglia, Marilena Florio, Marco Antonio Rosato, Antonio Corbo, Filomena Franchini, Carlo Musio, Biagia Degennaro, Leonardo Luisi, Renzo |
author_facet | Giovine, Arianna Muraglia, Marilena Florio, Marco Antonio Rosato, Antonio Corbo, Filomena Franchini, Carlo Musio, Biagia Degennaro, Leonardo Luisi, Renzo |
author_sort | Giovine, Arianna |
collection | PubMed |
description | By using the Suzuki-Miyaura protocol, a simple straightforward synthesis of functionalized 2-arylaziridines has been developed. By means of this synthetic strategy from readily available ortho-, meta- and para-bromophenylaziridines and aryl- or heteroarylboronic acids, new aziridines could be obtained. The cross-coupling reactions occurred without ring opening of the three membered ring. Preliminary results on the antimicrobial activity of the heterosubstituted biaryl compounds have been also included. |
format | Online Article Text |
id | pubmed-6271868 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62718682018-12-27 Synthesis of Functionalized Arylaziridines as Potential Antimicrobial Agents Giovine, Arianna Muraglia, Marilena Florio, Marco Antonio Rosato, Antonio Corbo, Filomena Franchini, Carlo Musio, Biagia Degennaro, Leonardo Luisi, Renzo Molecules Article By using the Suzuki-Miyaura protocol, a simple straightforward synthesis of functionalized 2-arylaziridines has been developed. By means of this synthetic strategy from readily available ortho-, meta- and para-bromophenylaziridines and aryl- or heteroarylboronic acids, new aziridines could be obtained. The cross-coupling reactions occurred without ring opening of the three membered ring. Preliminary results on the antimicrobial activity of the heterosubstituted biaryl compounds have been also included. MDPI 2014-08-04 /pmc/articles/PMC6271868/ /pubmed/25093988 http://dx.doi.org/10.3390/molecules190811505 Text en © 2014 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Giovine, Arianna Muraglia, Marilena Florio, Marco Antonio Rosato, Antonio Corbo, Filomena Franchini, Carlo Musio, Biagia Degennaro, Leonardo Luisi, Renzo Synthesis of Functionalized Arylaziridines as Potential Antimicrobial Agents |
title | Synthesis of Functionalized Arylaziridines as Potential Antimicrobial Agents |
title_full | Synthesis of Functionalized Arylaziridines as Potential Antimicrobial Agents |
title_fullStr | Synthesis of Functionalized Arylaziridines as Potential Antimicrobial Agents |
title_full_unstemmed | Synthesis of Functionalized Arylaziridines as Potential Antimicrobial Agents |
title_short | Synthesis of Functionalized Arylaziridines as Potential Antimicrobial Agents |
title_sort | synthesis of functionalized arylaziridines as potential antimicrobial agents |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271868/ https://www.ncbi.nlm.nih.gov/pubmed/25093988 http://dx.doi.org/10.3390/molecules190811505 |
work_keys_str_mv | AT giovinearianna synthesisoffunctionalizedarylaziridinesaspotentialantimicrobialagents AT muragliamarilena synthesisoffunctionalizedarylaziridinesaspotentialantimicrobialagents AT floriomarcoantonio synthesisoffunctionalizedarylaziridinesaspotentialantimicrobialagents AT rosatoantonio synthesisoffunctionalizedarylaziridinesaspotentialantimicrobialagents AT corbofilomena synthesisoffunctionalizedarylaziridinesaspotentialantimicrobialagents AT franchinicarlo synthesisoffunctionalizedarylaziridinesaspotentialantimicrobialagents AT musiobiagia synthesisoffunctionalizedarylaziridinesaspotentialantimicrobialagents AT degennaroleonardo synthesisoffunctionalizedarylaziridinesaspotentialantimicrobialagents AT luisirenzo synthesisoffunctionalizedarylaziridinesaspotentialantimicrobialagents |