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Brønsted Acid‐Catalysed Dehydrative Substitution Reactions of Alcohols
The direct, catalytic dehydrative substitution of alcohols is a challenging, yet highly desirable process in the development of more sustainable approaches to organic chemistry. This review outlines recent advances in Brønsted acid‐catalysed dehydrative substitution reactions for C−C, C−O, C−N and C...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
John Wiley and Sons Inc.
2020
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7820959/ https://www.ncbi.nlm.nih.gov/pubmed/32491202 http://dx.doi.org/10.1002/chem.202002106 |
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| author | Estopiñá‐Durán, Susana Taylor, James E. |
| author_facet | Estopiñá‐Durán, Susana Taylor, James E. |
| author_sort | Estopiñá‐Durán, Susana |
| collection | PubMed |
| description | The direct, catalytic dehydrative substitution of alcohols is a challenging, yet highly desirable process in the development of more sustainable approaches to organic chemistry. This review outlines recent advances in Brønsted acid‐catalysed dehydrative substitution reactions for C−C, C−O, C−N and C−S bond formation. The wide range of processes that are now accessible using simple alcohols as the formal electrophile are highlighted, while current limitations and therefore possible future directions for research are also discussed. |
| format | Online Article Text |
| id | pubmed-7820959 |
| institution | National Center for Biotechnology Information |
| language | English |
| publishDate | 2020 |
| publisher | John Wiley and Sons Inc. |
| record_format | MEDLINE/PubMed |
| spelling | pubmed-78209592021-01-26 Brønsted Acid‐Catalysed Dehydrative Substitution Reactions of Alcohols Estopiñá‐Durán, Susana Taylor, James E. Chemistry Minireviews The direct, catalytic dehydrative substitution of alcohols is a challenging, yet highly desirable process in the development of more sustainable approaches to organic chemistry. This review outlines recent advances in Brønsted acid‐catalysed dehydrative substitution reactions for C−C, C−O, C−N and C−S bond formation. The wide range of processes that are now accessible using simple alcohols as the formal electrophile are highlighted, while current limitations and therefore possible future directions for research are also discussed. John Wiley and Sons Inc. 2020-10-15 2021-01-04 /pmc/articles/PMC7820959/ /pubmed/32491202 http://dx.doi.org/10.1002/chem.202002106 Text en © 2020 The Authors. Published by Wiley-VCH GmbH This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
| spellingShingle | Minireviews Estopiñá‐Durán, Susana Taylor, James E. Brønsted Acid‐Catalysed Dehydrative Substitution Reactions of Alcohols |
| title | Brønsted Acid‐Catalysed Dehydrative Substitution Reactions of Alcohols |
| title_full | Brønsted Acid‐Catalysed Dehydrative Substitution Reactions of Alcohols |
| title_fullStr | Brønsted Acid‐Catalysed Dehydrative Substitution Reactions of Alcohols |
| title_full_unstemmed | Brønsted Acid‐Catalysed Dehydrative Substitution Reactions of Alcohols |
| title_short | Brønsted Acid‐Catalysed Dehydrative Substitution Reactions of Alcohols |
| title_sort | brønsted acid‐catalysed dehydrative substitution reactions of alcohols |
| topic | Minireviews |
| url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7820959/ https://www.ncbi.nlm.nih.gov/pubmed/32491202 http://dx.doi.org/10.1002/chem.202002106 |
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