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Asymmetric transformations from sulfoxonium ylides
Sulfoxonium ylides are important surrogates for diazo compounds, and their use in industry as safer alternatives has been evaluated during recent years. Beyond the known classical transformations, these ylides have also been used in a surprising plethora of novel and intrinsic chemical reactions, es...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8809404/ https://www.ncbi.nlm.nih.gov/pubmed/35222906 http://dx.doi.org/10.1039/d1sc05708a |
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author | Caiuby, Clarice A. D. Furniel, Lucas G. Burtoloso, Antonio C. B. |
author_facet | Caiuby, Clarice A. D. Furniel, Lucas G. Burtoloso, Antonio C. B. |
author_sort | Caiuby, Clarice A. D. |
collection | PubMed |
description | Sulfoxonium ylides are important surrogates for diazo compounds, and their use in industry as safer alternatives has been evaluated during recent years. Beyond the known classical transformations, these ylides have also been used in a surprising plethora of novel and intrinsic chemical reactions, especially in recent years. Bench stability and handling are also an advantage of this class of organosulfur molecules. Despite this, efficient asymmetric transformations, specifically catalytic enantioselective versions, have only recently been reported, and there are specific reasons for this. This perspective article covers this topic from the first studies up to the latest advances, giving personal perspectives and showing the main challenges in this area in the coming years. |
format | Online Article Text |
id | pubmed-8809404 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-88094042022-02-24 Asymmetric transformations from sulfoxonium ylides Caiuby, Clarice A. D. Furniel, Lucas G. Burtoloso, Antonio C. B. Chem Sci Chemistry Sulfoxonium ylides are important surrogates for diazo compounds, and their use in industry as safer alternatives has been evaluated during recent years. Beyond the known classical transformations, these ylides have also been used in a surprising plethora of novel and intrinsic chemical reactions, especially in recent years. Bench stability and handling are also an advantage of this class of organosulfur molecules. Despite this, efficient asymmetric transformations, specifically catalytic enantioselective versions, have only recently been reported, and there are specific reasons for this. This perspective article covers this topic from the first studies up to the latest advances, giving personal perspectives and showing the main challenges in this area in the coming years. The Royal Society of Chemistry 2021-12-08 /pmc/articles/PMC8809404/ /pubmed/35222906 http://dx.doi.org/10.1039/d1sc05708a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Caiuby, Clarice A. D. Furniel, Lucas G. Burtoloso, Antonio C. B. Asymmetric transformations from sulfoxonium ylides |
title | Asymmetric transformations from sulfoxonium ylides |
title_full | Asymmetric transformations from sulfoxonium ylides |
title_fullStr | Asymmetric transformations from sulfoxonium ylides |
title_full_unstemmed | Asymmetric transformations from sulfoxonium ylides |
title_short | Asymmetric transformations from sulfoxonium ylides |
title_sort | asymmetric transformations from sulfoxonium ylides |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8809404/ https://www.ncbi.nlm.nih.gov/pubmed/35222906 http://dx.doi.org/10.1039/d1sc05708a |
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