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Aminodifluorosulfinium Salts: Selective Fluorination Reagents with Enhanced Thermal Stability and Ease of Handling(,)
[Image: see text] Diethylaminodifluorosulfinium tetrafluoroborate (XtalFluor-E) and morpholinodifluorosulfinium tetrafluoroborate (XtalFluor-M) are crystalline fluorinating agents that are more easily handled and significantly more stable than Deoxo-Fluor, DAST, and their analogues. These reagents c...
Autores principales: | , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2869536/ https://www.ncbi.nlm.nih.gov/pubmed/20405933 http://dx.doi.org/10.1021/jo100504x |
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author | L’Heureux, Alexandre Beaulieu, Francis Bennett, Christopher Bill, David R. Clayton, Simon LaFlamme, François Mirmehrabi, Mahmoud Tadayon, Sam Tovell, David Couturier, Michel |
author_facet | L’Heureux, Alexandre Beaulieu, Francis Bennett, Christopher Bill, David R. Clayton, Simon LaFlamme, François Mirmehrabi, Mahmoud Tadayon, Sam Tovell, David Couturier, Michel |
author_sort | L’Heureux, Alexandre |
collection | PubMed |
description | [Image: see text] Diethylaminodifluorosulfinium tetrafluoroborate (XtalFluor-E) and morpholinodifluorosulfinium tetrafluoroborate (XtalFluor-M) are crystalline fluorinating agents that are more easily handled and significantly more stable than Deoxo-Fluor, DAST, and their analogues. These reagents can be prepared in a safer and more cost-efficient manner by avoiding the laborious and hazardous distillation of dialkylaminosulfur trifluorides. Unlike DAST, Deoxo-Fluor, and Fluolead, XtalFluor reagents do not generate highly corrosive free-HF and therefore can be used in standard borosilicate vessels. When used in conjunction with promoters such as Et(3)N·3HF, Et(3)N·2HF, or DBU, XtalFluor reagents effectively convert alcohols to alkyl fluorides and carbonyls to gem-difluorides. These reagents are typically more selective than DAST and Deoxo-Fluor and exhibit superior performance by providing significantly less elimination side products. |
format | Text |
id | pubmed-2869536 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-28695362010-05-14 Aminodifluorosulfinium Salts: Selective Fluorination Reagents with Enhanced Thermal Stability and Ease of Handling(,) L’Heureux, Alexandre Beaulieu, Francis Bennett, Christopher Bill, David R. Clayton, Simon LaFlamme, François Mirmehrabi, Mahmoud Tadayon, Sam Tovell, David Couturier, Michel J Org Chem [Image: see text] Diethylaminodifluorosulfinium tetrafluoroborate (XtalFluor-E) and morpholinodifluorosulfinium tetrafluoroborate (XtalFluor-M) are crystalline fluorinating agents that are more easily handled and significantly more stable than Deoxo-Fluor, DAST, and their analogues. These reagents can be prepared in a safer and more cost-efficient manner by avoiding the laborious and hazardous distillation of dialkylaminosulfur trifluorides. Unlike DAST, Deoxo-Fluor, and Fluolead, XtalFluor reagents do not generate highly corrosive free-HF and therefore can be used in standard borosilicate vessels. When used in conjunction with promoters such as Et(3)N·3HF, Et(3)N·2HF, or DBU, XtalFluor reagents effectively convert alcohols to alkyl fluorides and carbonyls to gem-difluorides. These reagents are typically more selective than DAST and Deoxo-Fluor and exhibit superior performance by providing significantly less elimination side products. American Chemical Society 2010-04-21 2010-05-21 /pmc/articles/PMC2869536/ /pubmed/20405933 http://dx.doi.org/10.1021/jo100504x Text en Copyright © 2010 American Chemical Society http://pubs.acs.org This is an open-access article distributed under the ACS AuthorChoice Terms & Conditions. Any use of this article, must conform to the terms of that license which are available at http://pubs.acs.org. |
spellingShingle | L’Heureux, Alexandre Beaulieu, Francis Bennett, Christopher Bill, David R. Clayton, Simon LaFlamme, François Mirmehrabi, Mahmoud Tadayon, Sam Tovell, David Couturier, Michel Aminodifluorosulfinium Salts: Selective Fluorination Reagents with Enhanced Thermal Stability and Ease of Handling(,) |
title | Aminodifluorosulfinium Salts: Selective Fluorination Reagents with Enhanced Thermal Stability and Ease of Handling(,) |
title_full | Aminodifluorosulfinium Salts: Selective Fluorination Reagents with Enhanced Thermal Stability and Ease of Handling(,) |
title_fullStr | Aminodifluorosulfinium Salts: Selective Fluorination Reagents with Enhanced Thermal Stability and Ease of Handling(,) |
title_full_unstemmed | Aminodifluorosulfinium Salts: Selective Fluorination Reagents with Enhanced Thermal Stability and Ease of Handling(,) |
title_short | Aminodifluorosulfinium Salts: Selective Fluorination Reagents with Enhanced Thermal Stability and Ease of Handling(,) |
title_sort | aminodifluorosulfinium salts: selective fluorination reagents with enhanced thermal stability and ease of handling(,) |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2869536/ https://www.ncbi.nlm.nih.gov/pubmed/20405933 http://dx.doi.org/10.1021/jo100504x |
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