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Synthesis of (E,E)-Dienones and (E,E)-Dienals via Palladium-Catalyzed γ,δ-Dehydrogenation of Enones and Enals
A new strategy for the synthesis of conjugated (E,E)-dienones and (E,E)-dienals via a palladium-catalyzed aerobic γ,δ-dehydrogenation of enones and enals has been developed. The method can be employed in the direct and efficient synthesis of various (E,E)-dienones and (E,E)-dienals, including non-su...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6817633/ https://www.ncbi.nlm.nih.gov/pubmed/31590075 http://dx.doi.org/10.1016/j.isci.2019.09.027 |
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author | Pan, Gao-Fei Zhang, Xing-Long Zhu, Xue-Qing Guo, Rui-Li Wang, Yong-Qiang |
author_facet | Pan, Gao-Fei Zhang, Xing-Long Zhu, Xue-Qing Guo, Rui-Li Wang, Yong-Qiang |
author_sort | Pan, Gao-Fei |
collection | PubMed |
description | A new strategy for the synthesis of conjugated (E,E)-dienones and (E,E)-dienals via a palladium-catalyzed aerobic γ,δ-dehydrogenation of enones and enals has been developed. The method can be employed in the direct and efficient synthesis of various (E,E)-dienones and (E,E)-dienals, including non-substituted α-, β-, and γ- and/or δ-substituted (E,E)-dienones and (E,E)-dienals. The protocol is featured by the ready accessibility and elaboration of the starting materials, good functional group compatibility, and mild reaction conditions. Furthermore, the reaction is of complete E,E-stereoselectivity and uses molecular oxygen as the sole clean oxidant. |
format | Online Article Text |
id | pubmed-6817633 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-68176332019-10-31 Synthesis of (E,E)-Dienones and (E,E)-Dienals via Palladium-Catalyzed γ,δ-Dehydrogenation of Enones and Enals Pan, Gao-Fei Zhang, Xing-Long Zhu, Xue-Qing Guo, Rui-Li Wang, Yong-Qiang iScience Article A new strategy for the synthesis of conjugated (E,E)-dienones and (E,E)-dienals via a palladium-catalyzed aerobic γ,δ-dehydrogenation of enones and enals has been developed. The method can be employed in the direct and efficient synthesis of various (E,E)-dienones and (E,E)-dienals, including non-substituted α-, β-, and γ- and/or δ-substituted (E,E)-dienones and (E,E)-dienals. The protocol is featured by the ready accessibility and elaboration of the starting materials, good functional group compatibility, and mild reaction conditions. Furthermore, the reaction is of complete E,E-stereoselectivity and uses molecular oxygen as the sole clean oxidant. Elsevier 2019-09-21 /pmc/articles/PMC6817633/ /pubmed/31590075 http://dx.doi.org/10.1016/j.isci.2019.09.027 Text en © 2019 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Pan, Gao-Fei Zhang, Xing-Long Zhu, Xue-Qing Guo, Rui-Li Wang, Yong-Qiang Synthesis of (E,E)-Dienones and (E,E)-Dienals via Palladium-Catalyzed γ,δ-Dehydrogenation of Enones and Enals |
title | Synthesis of (E,E)-Dienones and (E,E)-Dienals via Palladium-Catalyzed γ,δ-Dehydrogenation of Enones and Enals |
title_full | Synthesis of (E,E)-Dienones and (E,E)-Dienals via Palladium-Catalyzed γ,δ-Dehydrogenation of Enones and Enals |
title_fullStr | Synthesis of (E,E)-Dienones and (E,E)-Dienals via Palladium-Catalyzed γ,δ-Dehydrogenation of Enones and Enals |
title_full_unstemmed | Synthesis of (E,E)-Dienones and (E,E)-Dienals via Palladium-Catalyzed γ,δ-Dehydrogenation of Enones and Enals |
title_short | Synthesis of (E,E)-Dienones and (E,E)-Dienals via Palladium-Catalyzed γ,δ-Dehydrogenation of Enones and Enals |
title_sort | synthesis of (e,e)-dienones and (e,e)-dienals via palladium-catalyzed γ,δ-dehydrogenation of enones and enals |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6817633/ https://www.ncbi.nlm.nih.gov/pubmed/31590075 http://dx.doi.org/10.1016/j.isci.2019.09.027 |
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