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New Insight into the Reactivity of S,S-Bis-ylide
The present work focuses on the reactivity of S,S-bis-ylide 2, which presents a strong nucleophilic character, as evidenced by reactions with methyl iodide and CO(2), affording C-methylated salts 3 and betaine 4, respectively. The derivatization of betaine 4 affords the corresponding ester derivativ...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10142965/ https://www.ncbi.nlm.nih.gov/pubmed/37110528 http://dx.doi.org/10.3390/molecules28083295 |
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author | Authesserre, Ugo Swamy, V. S. V. S. N. Saffon-Merceron, Nathalie Baceiredo, Antoine Kato, Tsuyoshi Maerten, Eddy |
author_facet | Authesserre, Ugo Swamy, V. S. V. S. N. Saffon-Merceron, Nathalie Baceiredo, Antoine Kato, Tsuyoshi Maerten, Eddy |
author_sort | Authesserre, Ugo |
collection | PubMed |
description | The present work focuses on the reactivity of S,S-bis-ylide 2, which presents a strong nucleophilic character, as evidenced by reactions with methyl iodide and CO(2), affording C-methylated salts 3 and betaine 4, respectively. The derivatization of betaine 4 affords the corresponding ester derivative 6, which is fully characterized by using NMR spectroscopy and X-ray diffraction analysis. Furthermore, an original reaction with phosphenium ions leads to the formation of a transient push–pull phosphino(sulfonio)carbene 8, which rearranges to give stabilized sulfonium ylide derivative 7. |
format | Online Article Text |
id | pubmed-10142965 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-101429652023-04-29 New Insight into the Reactivity of S,S-Bis-ylide Authesserre, Ugo Swamy, V. S. V. S. N. Saffon-Merceron, Nathalie Baceiredo, Antoine Kato, Tsuyoshi Maerten, Eddy Molecules Article The present work focuses on the reactivity of S,S-bis-ylide 2, which presents a strong nucleophilic character, as evidenced by reactions with methyl iodide and CO(2), affording C-methylated salts 3 and betaine 4, respectively. The derivatization of betaine 4 affords the corresponding ester derivative 6, which is fully characterized by using NMR spectroscopy and X-ray diffraction analysis. Furthermore, an original reaction with phosphenium ions leads to the formation of a transient push–pull phosphino(sulfonio)carbene 8, which rearranges to give stabilized sulfonium ylide derivative 7. MDPI 2023-04-07 /pmc/articles/PMC10142965/ /pubmed/37110528 http://dx.doi.org/10.3390/molecules28083295 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Authesserre, Ugo Swamy, V. S. V. S. N. Saffon-Merceron, Nathalie Baceiredo, Antoine Kato, Tsuyoshi Maerten, Eddy New Insight into the Reactivity of S,S-Bis-ylide |
title | New Insight into the Reactivity of S,S-Bis-ylide |
title_full | New Insight into the Reactivity of S,S-Bis-ylide |
title_fullStr | New Insight into the Reactivity of S,S-Bis-ylide |
title_full_unstemmed | New Insight into the Reactivity of S,S-Bis-ylide |
title_short | New Insight into the Reactivity of S,S-Bis-ylide |
title_sort | new insight into the reactivity of s,s-bis-ylide |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10142965/ https://www.ncbi.nlm.nih.gov/pubmed/37110528 http://dx.doi.org/10.3390/molecules28083295 |
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