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Periselectivity in the Aza-Diels–Alder Reaction of 1-Azadienes with α-Oxoketenes: A Combined Experimental and Theoretical Study

Inversions in the periselectivity of formal aza-Diels–Alder cycloadditions between α-oxoketenes generated by a thermally-induced Wolff rearrangement and 1-azadienes were observed experimentally as a function of the α-oxoketene and the 1-azadiene, as well as the reaction temperature and time. Some un...

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Autores principales: Presset, Marc, Rajzmann, Michel, Dauvergne, Guillaume, Rodriguez, Jean, Coquerel, Yoann
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7587935/
https://www.ncbi.nlm.nih.gov/pubmed/33092017
http://dx.doi.org/10.3390/molecules25204811
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author Presset, Marc
Rajzmann, Michel
Dauvergne, Guillaume
Rodriguez, Jean
Coquerel, Yoann
author_facet Presset, Marc
Rajzmann, Michel
Dauvergne, Guillaume
Rodriguez, Jean
Coquerel, Yoann
author_sort Presset, Marc
collection PubMed
description Inversions in the periselectivity of formal aza-Diels–Alder cycloadditions between α-oxoketenes generated by a thermally-induced Wolff rearrangement and 1-azadienes were observed experimentally as a function of the α-oxoketene and the 1-azadiene, as well as the reaction temperature and time. Some unexpected inversion in the diastereoselectivity was observed, too. These variations in selectivities were fully rationalized by computational modeling using density functional theory (DFT) methods.
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spelling pubmed-75879352020-10-29 Periselectivity in the Aza-Diels–Alder Reaction of 1-Azadienes with α-Oxoketenes: A Combined Experimental and Theoretical Study Presset, Marc Rajzmann, Michel Dauvergne, Guillaume Rodriguez, Jean Coquerel, Yoann Molecules Article Inversions in the periselectivity of formal aza-Diels–Alder cycloadditions between α-oxoketenes generated by a thermally-induced Wolff rearrangement and 1-azadienes were observed experimentally as a function of the α-oxoketene and the 1-azadiene, as well as the reaction temperature and time. Some unexpected inversion in the diastereoselectivity was observed, too. These variations in selectivities were fully rationalized by computational modeling using density functional theory (DFT) methods. MDPI 2020-10-20 /pmc/articles/PMC7587935/ /pubmed/33092017 http://dx.doi.org/10.3390/molecules25204811 Text en © 2020 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 (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Presset, Marc
Rajzmann, Michel
Dauvergne, Guillaume
Rodriguez, Jean
Coquerel, Yoann
Periselectivity in the Aza-Diels–Alder Reaction of 1-Azadienes with α-Oxoketenes: A Combined Experimental and Theoretical Study
title Periselectivity in the Aza-Diels–Alder Reaction of 1-Azadienes with α-Oxoketenes: A Combined Experimental and Theoretical Study
title_full Periselectivity in the Aza-Diels–Alder Reaction of 1-Azadienes with α-Oxoketenes: A Combined Experimental and Theoretical Study
title_fullStr Periselectivity in the Aza-Diels–Alder Reaction of 1-Azadienes with α-Oxoketenes: A Combined Experimental and Theoretical Study
title_full_unstemmed Periselectivity in the Aza-Diels–Alder Reaction of 1-Azadienes with α-Oxoketenes: A Combined Experimental and Theoretical Study
title_short Periselectivity in the Aza-Diels–Alder Reaction of 1-Azadienes with α-Oxoketenes: A Combined Experimental and Theoretical Study
title_sort periselectivity in the aza-diels–alder reaction of 1-azadienes with α-oxoketenes: a combined experimental and theoretical study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7587935/
https://www.ncbi.nlm.nih.gov/pubmed/33092017
http://dx.doi.org/10.3390/molecules25204811
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