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Continuous-flow retro-Diels–Alder reaction: an efficient method for the preparation of pyrimidinone derivatives

The syntheses of various pyrimidinones as potentially bioactive products by means of the highly controlled continuous-flow retro-Diels–Alder reaction of condensed pyrimidinone derivatives are presented. Noteworthy, the use of this approach allowed us to rapidly screen a selection of conditions and q...

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Autores principales: Nekkaa, Imane, Palkó, Márta, Mándity, István M, Fülöp, Ferenc
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5815275/
https://www.ncbi.nlm.nih.gov/pubmed/29507637
http://dx.doi.org/10.3762/bjoc.14.20
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author Nekkaa, Imane
Palkó, Márta
Mándity, István M
Fülöp, Ferenc
author_facet Nekkaa, Imane
Palkó, Márta
Mándity, István M
Fülöp, Ferenc
author_sort Nekkaa, Imane
collection PubMed
description The syntheses of various pyrimidinones as potentially bioactive products by means of the highly controlled continuous-flow retro-Diels–Alder reaction of condensed pyrimidinone derivatives are presented. Noteworthy, the use of this approach allowed us to rapidly screen a selection of conditions and quickly confirm the viability of preparing the desired pyrimidinones in short reaction times. Yields typically higher than those published earlier using conventional batch or microwave processes were achieved.
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spelling pubmed-58152752018-03-05 Continuous-flow retro-Diels–Alder reaction: an efficient method for the preparation of pyrimidinone derivatives Nekkaa, Imane Palkó, Márta Mándity, István M Fülöp, Ferenc Beilstein J Org Chem Full Research Paper The syntheses of various pyrimidinones as potentially bioactive products by means of the highly controlled continuous-flow retro-Diels–Alder reaction of condensed pyrimidinone derivatives are presented. Noteworthy, the use of this approach allowed us to rapidly screen a selection of conditions and quickly confirm the viability of preparing the desired pyrimidinones in short reaction times. Yields typically higher than those published earlier using conventional batch or microwave processes were achieved. Beilstein-Institut 2018-02-01 /pmc/articles/PMC5815275/ /pubmed/29507637 http://dx.doi.org/10.3762/bjoc.14.20 Text en Copyright © 2018, Nekkaa et al. https://creativecommons.org/licenses/by/4.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Full Research Paper
Nekkaa, Imane
Palkó, Márta
Mándity, István M
Fülöp, Ferenc
Continuous-flow retro-Diels–Alder reaction: an efficient method for the preparation of pyrimidinone derivatives
title Continuous-flow retro-Diels–Alder reaction: an efficient method for the preparation of pyrimidinone derivatives
title_full Continuous-flow retro-Diels–Alder reaction: an efficient method for the preparation of pyrimidinone derivatives
title_fullStr Continuous-flow retro-Diels–Alder reaction: an efficient method for the preparation of pyrimidinone derivatives
title_full_unstemmed Continuous-flow retro-Diels–Alder reaction: an efficient method for the preparation of pyrimidinone derivatives
title_short Continuous-flow retro-Diels–Alder reaction: an efficient method for the preparation of pyrimidinone derivatives
title_sort continuous-flow retro-diels–alder reaction: an efficient method for the preparation of pyrimidinone derivatives
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5815275/
https://www.ncbi.nlm.nih.gov/pubmed/29507637
http://dx.doi.org/10.3762/bjoc.14.20
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