Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: L’Heureux, Alexandre, Beaulieu, Francis, Bennett, Christopher, Bill, David R., Clayton, Simon, LaFlamme, François, Mirmehrabi, Mahmoud, Tadayon, Sam, Tovell, David, Couturier, Michel
Formato: Texto
Lenguaje:English
Publicado: American Chemical Society 2010
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
_version_ 1782181132262965248
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
work_keys_str_mv AT lheureuxalexandre aminodifluorosulfiniumsaltsselectivefluorinationreagentswithenhancedthermalstabilityandeaseofhandling
AT beaulieufrancis aminodifluorosulfiniumsaltsselectivefluorinationreagentswithenhancedthermalstabilityandeaseofhandling
AT bennettchristopher aminodifluorosulfiniumsaltsselectivefluorinationreagentswithenhancedthermalstabilityandeaseofhandling
AT billdavidr aminodifluorosulfiniumsaltsselectivefluorinationreagentswithenhancedthermalstabilityandeaseofhandling
AT claytonsimon aminodifluorosulfiniumsaltsselectivefluorinationreagentswithenhancedthermalstabilityandeaseofhandling
AT laflammefrancois aminodifluorosulfiniumsaltsselectivefluorinationreagentswithenhancedthermalstabilityandeaseofhandling
AT mirmehrabimahmoud aminodifluorosulfiniumsaltsselectivefluorinationreagentswithenhancedthermalstabilityandeaseofhandling
AT tadayonsam aminodifluorosulfiniumsaltsselectivefluorinationreagentswithenhancedthermalstabilityandeaseofhandling
AT tovelldavid aminodifluorosulfiniumsaltsselectivefluorinationreagentswithenhancedthermalstabilityandeaseofhandling
AT couturiermichel aminodifluorosulfiniumsaltsselectivefluorinationreagentswithenhancedthermalstabilityandeaseofhandling