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Manganese-Mediated Coupling Reaction of Vinylarenes and Aliphatic Alcohols
Alcohols and alkenes are the most abundant and commonly used organic building blocks in the large-scale chemical synthesis. Herein, this is the first time to report a novel and operationally simple coupling reaction of vinylarenes and aliphatic alcohols catalyzed by manganese in the presence of TBHP...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4607950/ https://www.ncbi.nlm.nih.gov/pubmed/26470633 http://dx.doi.org/10.1038/srep15250 |
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author | Zhang, Wei Wang, Nai-Xing Bai, Cui-Bing Wang, Yan-Jing Lan, Xing-Wang Xing, Yalan Li, Yi-He Wen, Jia-Long |
author_facet | Zhang, Wei Wang, Nai-Xing Bai, Cui-Bing Wang, Yan-Jing Lan, Xing-Wang Xing, Yalan Li, Yi-He Wen, Jia-Long |
author_sort | Zhang, Wei |
collection | PubMed |
description | Alcohols and alkenes are the most abundant and commonly used organic building blocks in the large-scale chemical synthesis. Herein, this is the first time to report a novel and operationally simple coupling reaction of vinylarenes and aliphatic alcohols catalyzed by manganese in the presence of TBHP (tert-butyl hydroperoxide). This coupling reaction provides the oxyalkylated products of vinylarenes with good regioselectivity and accomplishes with the principles of step-economies. A possible reaction mechanism has also been proposed. |
format | Online Article Text |
id | pubmed-4607950 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-46079502015-10-28 Manganese-Mediated Coupling Reaction of Vinylarenes and Aliphatic Alcohols Zhang, Wei Wang, Nai-Xing Bai, Cui-Bing Wang, Yan-Jing Lan, Xing-Wang Xing, Yalan Li, Yi-He Wen, Jia-Long Sci Rep Article Alcohols and alkenes are the most abundant and commonly used organic building blocks in the large-scale chemical synthesis. Herein, this is the first time to report a novel and operationally simple coupling reaction of vinylarenes and aliphatic alcohols catalyzed by manganese in the presence of TBHP (tert-butyl hydroperoxide). This coupling reaction provides the oxyalkylated products of vinylarenes with good regioselectivity and accomplishes with the principles of step-economies. A possible reaction mechanism has also been proposed. Nature Publishing Group 2015-10-16 /pmc/articles/PMC4607950/ /pubmed/26470633 http://dx.doi.org/10.1038/srep15250 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Zhang, Wei Wang, Nai-Xing Bai, Cui-Bing Wang, Yan-Jing Lan, Xing-Wang Xing, Yalan Li, Yi-He Wen, Jia-Long Manganese-Mediated Coupling Reaction of Vinylarenes and Aliphatic Alcohols |
title | Manganese-Mediated Coupling Reaction of Vinylarenes and Aliphatic Alcohols |
title_full | Manganese-Mediated Coupling Reaction of Vinylarenes and Aliphatic Alcohols |
title_fullStr | Manganese-Mediated Coupling Reaction of Vinylarenes and Aliphatic Alcohols |
title_full_unstemmed | Manganese-Mediated Coupling Reaction of Vinylarenes and Aliphatic Alcohols |
title_short | Manganese-Mediated Coupling Reaction of Vinylarenes and Aliphatic Alcohols |
title_sort | manganese-mediated coupling reaction of vinylarenes and aliphatic alcohols |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4607950/ https://www.ncbi.nlm.nih.gov/pubmed/26470633 http://dx.doi.org/10.1038/srep15250 |
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