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DBU Promoted Polysubstituted Arene Formation via a Michael Addition/Cyclization/Elimination Cascade Reaction
The straightforward construction of polysubstituted arenes is essential in both synthetic chemistry and medicinal chemistry. Herein, we reported a DBU promoted Michael addition/cyclization/elimination cascade reaction between vinylogous malononitrile derivatives and chlorinated nitrostyrenes for the...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9738611/ https://www.ncbi.nlm.nih.gov/pubmed/36500260 http://dx.doi.org/10.3390/molecules27238167 |
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author | Bai, Guishun Yang, Yang Wang, Xingyue Wu, Jiamin Wang, Hong Ye, Xinyi Bao, Xiaoze |
author_facet | Bai, Guishun Yang, Yang Wang, Xingyue Wu, Jiamin Wang, Hong Ye, Xinyi Bao, Xiaoze |
author_sort | Bai, Guishun |
collection | PubMed |
description | The straightforward construction of polysubstituted arenes is essential in both synthetic chemistry and medicinal chemistry. Herein, we reported a DBU promoted Michael addition/cyclization/elimination cascade reaction between vinylogous malononitrile derivatives and chlorinated nitrostyrenes for the synthesis of polysubstituted arenes. The method features mild reaction conditions, wide substrate scope and high yield. Interestingly, preliminary study of the enantioselective version of this cascade was conducted to give chiral biaryl atropisomers with up to 40% ee through center-to-axial chirality transfer strategy. |
format | Online Article Text |
id | pubmed-9738611 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-97386112022-12-11 DBU Promoted Polysubstituted Arene Formation via a Michael Addition/Cyclization/Elimination Cascade Reaction Bai, Guishun Yang, Yang Wang, Xingyue Wu, Jiamin Wang, Hong Ye, Xinyi Bao, Xiaoze Molecules Communication The straightforward construction of polysubstituted arenes is essential in both synthetic chemistry and medicinal chemistry. Herein, we reported a DBU promoted Michael addition/cyclization/elimination cascade reaction between vinylogous malononitrile derivatives and chlorinated nitrostyrenes for the synthesis of polysubstituted arenes. The method features mild reaction conditions, wide substrate scope and high yield. Interestingly, preliminary study of the enantioselective version of this cascade was conducted to give chiral biaryl atropisomers with up to 40% ee through center-to-axial chirality transfer strategy. MDPI 2022-11-23 /pmc/articles/PMC9738611/ /pubmed/36500260 http://dx.doi.org/10.3390/molecules27238167 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Communication Bai, Guishun Yang, Yang Wang, Xingyue Wu, Jiamin Wang, Hong Ye, Xinyi Bao, Xiaoze DBU Promoted Polysubstituted Arene Formation via a Michael Addition/Cyclization/Elimination Cascade Reaction |
title | DBU Promoted Polysubstituted Arene Formation via a Michael Addition/Cyclization/Elimination Cascade Reaction |
title_full | DBU Promoted Polysubstituted Arene Formation via a Michael Addition/Cyclization/Elimination Cascade Reaction |
title_fullStr | DBU Promoted Polysubstituted Arene Formation via a Michael Addition/Cyclization/Elimination Cascade Reaction |
title_full_unstemmed | DBU Promoted Polysubstituted Arene Formation via a Michael Addition/Cyclization/Elimination Cascade Reaction |
title_short | DBU Promoted Polysubstituted Arene Formation via a Michael Addition/Cyclization/Elimination Cascade Reaction |
title_sort | dbu promoted polysubstituted arene formation via a michael addition/cyclization/elimination cascade reaction |
topic | Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9738611/ https://www.ncbi.nlm.nih.gov/pubmed/36500260 http://dx.doi.org/10.3390/molecules27238167 |
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