TDAE Strategy in the Benzoxazolone Series: Synthesis and Reactivity of a New Benzoxazolinonic Anion

We describe an original pathway to produce new 5-substituted 3-methyl-6-nitro-benzoxazolones by the reaction of aromatic carbonyl and α-carbonyl ester derivatives with a benzoxazolinonic anion formed exclusively via the TDAE strategy.

Detalles Bibliográficos
Autores principales: Nadji-Boukrouche, Aïda R., Khoumeri, Omar, Terme, Thierry, Liacha, Messaoud, Vanelle, Patrice
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2015
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272611/
https://www.ncbi.nlm.nih.gov/pubmed/25594341
http://dx.doi.org/10.3390/molecules20011262
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author Nadji-Boukrouche, Aïda R.
Khoumeri, Omar
Terme, Thierry
Liacha, Messaoud
Vanelle, Patrice
author_facet Nadji-Boukrouche, Aïda R.
Khoumeri, Omar
Terme, Thierry
Liacha, Messaoud
Vanelle, Patrice
author_sort Nadji-Boukrouche, Aïda R.
collection PubMed
description We describe an original pathway to produce new 5-substituted 3-methyl-6-nitro-benzoxazolones by the reaction of aromatic carbonyl and α-carbonyl ester derivatives with a benzoxazolinonic anion formed exclusively via the TDAE strategy.
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spelling pubmed-62726112018-12-28 TDAE Strategy in the Benzoxazolone Series: Synthesis and Reactivity of a New Benzoxazolinonic Anion Nadji-Boukrouche, Aïda R. Khoumeri, Omar Terme, Thierry Liacha, Messaoud Vanelle, Patrice Molecules Article We describe an original pathway to produce new 5-substituted 3-methyl-6-nitro-benzoxazolones by the reaction of aromatic carbonyl and α-carbonyl ester derivatives with a benzoxazolinonic anion formed exclusively via the TDAE strategy. MDPI 2015-01-14 /pmc/articles/PMC6272611/ /pubmed/25594341 http://dx.doi.org/10.3390/molecules20011262 Text en © 2015 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/4.0/).
spellingShingle Article
Nadji-Boukrouche, Aïda R.
Khoumeri, Omar
Terme, Thierry
Liacha, Messaoud
Vanelle, Patrice
TDAE Strategy in the Benzoxazolone Series: Synthesis and Reactivity of a New Benzoxazolinonic Anion
title TDAE Strategy in the Benzoxazolone Series: Synthesis and Reactivity of a New Benzoxazolinonic Anion
title_full TDAE Strategy in the Benzoxazolone Series: Synthesis and Reactivity of a New Benzoxazolinonic Anion
title_fullStr TDAE Strategy in the Benzoxazolone Series: Synthesis and Reactivity of a New Benzoxazolinonic Anion
title_full_unstemmed TDAE Strategy in the Benzoxazolone Series: Synthesis and Reactivity of a New Benzoxazolinonic Anion
title_short TDAE Strategy in the Benzoxazolone Series: Synthesis and Reactivity of a New Benzoxazolinonic Anion
title_sort tdae strategy in the benzoxazolone series: synthesis and reactivity of a new benzoxazolinonic anion
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272611/
https://www.ncbi.nlm.nih.gov/pubmed/25594341
http://dx.doi.org/10.3390/molecules20011262
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