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Mechanochemical synthesis of magnesium-based carbon nucleophiles in air and their use in organic synthesis
Since the discovery of Grignard reagents in 1900, the nucleophilic addition of magnesium-based carbon nucleophiles to various electrophiles has become one of the most powerful, versatile, and well-established methods for the formation of carbon−carbon bonds in organic synthesis. Grignard reagents ar...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8602241/ https://www.ncbi.nlm.nih.gov/pubmed/34795265 http://dx.doi.org/10.1038/s41467-021-26962-w |
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author | Takahashi, Rina Hu, Anqi Gao, Pan Gao, Yunpeng Pang, Yadong Seo, Tamae Jiang, Julong Maeda, Satoshi Takaya, Hikaru Kubota, Koji Ito, Hajime |
author_facet | Takahashi, Rina Hu, Anqi Gao, Pan Gao, Yunpeng Pang, Yadong Seo, Tamae Jiang, Julong Maeda, Satoshi Takaya, Hikaru Kubota, Koji Ito, Hajime |
author_sort | Takahashi, Rina |
collection | PubMed |
description | Since the discovery of Grignard reagents in 1900, the nucleophilic addition of magnesium-based carbon nucleophiles to various electrophiles has become one of the most powerful, versatile, and well-established methods for the formation of carbon−carbon bonds in organic synthesis. Grignard reagents are typically prepared via reactions between organic halides and magnesium metal in a solvent. However, this method usually requires the use of dry organic solvents, long reaction times, strict control of the reaction temperature, and inert-gas-line techniques. Despite the utility of Grignard reagents, these requirements still represent major drawbacks from both an environmental and an economic perspective, and often cause reproducibility problems. Here, we report the general mechanochemical synthesis of magnesium-based carbon nucleophiles (Grignard reagents in paste form) in air using a ball milling technique. These nucleophiles can be used directly for one-pot nucleophilic addition reactions with various electrophiles and nickel-catalyzed cross-coupling reactions under solvent-free conditions. |
format | Online Article Text |
id | pubmed-8602241 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-86022412021-11-19 Mechanochemical synthesis of magnesium-based carbon nucleophiles in air and their use in organic synthesis Takahashi, Rina Hu, Anqi Gao, Pan Gao, Yunpeng Pang, Yadong Seo, Tamae Jiang, Julong Maeda, Satoshi Takaya, Hikaru Kubota, Koji Ito, Hajime Nat Commun Article Since the discovery of Grignard reagents in 1900, the nucleophilic addition of magnesium-based carbon nucleophiles to various electrophiles has become one of the most powerful, versatile, and well-established methods for the formation of carbon−carbon bonds in organic synthesis. Grignard reagents are typically prepared via reactions between organic halides and magnesium metal in a solvent. However, this method usually requires the use of dry organic solvents, long reaction times, strict control of the reaction temperature, and inert-gas-line techniques. Despite the utility of Grignard reagents, these requirements still represent major drawbacks from both an environmental and an economic perspective, and often cause reproducibility problems. Here, we report the general mechanochemical synthesis of magnesium-based carbon nucleophiles (Grignard reagents in paste form) in air using a ball milling technique. These nucleophiles can be used directly for one-pot nucleophilic addition reactions with various electrophiles and nickel-catalyzed cross-coupling reactions under solvent-free conditions. Nature Publishing Group UK 2021-11-18 /pmc/articles/PMC8602241/ /pubmed/34795265 http://dx.doi.org/10.1038/s41467-021-26962-w Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Takahashi, Rina Hu, Anqi Gao, Pan Gao, Yunpeng Pang, Yadong Seo, Tamae Jiang, Julong Maeda, Satoshi Takaya, Hikaru Kubota, Koji Ito, Hajime Mechanochemical synthesis of magnesium-based carbon nucleophiles in air and their use in organic synthesis |
title | Mechanochemical synthesis of magnesium-based carbon nucleophiles in air and their use in organic synthesis |
title_full | Mechanochemical synthesis of magnesium-based carbon nucleophiles in air and their use in organic synthesis |
title_fullStr | Mechanochemical synthesis of magnesium-based carbon nucleophiles in air and their use in organic synthesis |
title_full_unstemmed | Mechanochemical synthesis of magnesium-based carbon nucleophiles in air and their use in organic synthesis |
title_short | Mechanochemical synthesis of magnesium-based carbon nucleophiles in air and their use in organic synthesis |
title_sort | mechanochemical synthesis of magnesium-based carbon nucleophiles in air and their use in organic synthesis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8602241/ https://www.ncbi.nlm.nih.gov/pubmed/34795265 http://dx.doi.org/10.1038/s41467-021-26962-w |
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