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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...

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Autores principales: Bai, Guishun, Yang, Yang, Wang, Xingyue, Wu, Jiamin, Wang, Hong, Ye, Xinyi, Bao, Xiaoze
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
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.
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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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