Sulfonyl fluorides as targets and substrates in the development of new synthetic methods
The advent of sulfur(VI)-fluoride exchange (SuFEx) processes as transformations with click-like reactivity has invigorated research into electrophilic species featuring a sulfur–fluorine bond. Among these, sulfonyl fluorides have emerged as the workhorse functional group, with diverse applications b...
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| 格式: | Journal article |
| 語言: | English |
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Springer Nature
2022
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| _version_ | 1826308189837066240 |
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| author | Lou, TS-B Willis, MC |
| author_facet | Lou, TS-B Willis, MC |
| author_sort | Lou, TS-B |
| collection | OXFORD |
| description | The advent of sulfur(VI)-fluoride exchange (SuFEx) processes as transformations with click-like reactivity has invigorated research into electrophilic species featuring a sulfur–fluorine bond. Among these, sulfonyl fluorides have emerged as the workhorse functional group, with diverse applications being reported. Sulfonyl fluorides are used as electrophilic warheads by both medicinal chemists and chemical biologists. The balance of reactivity and stability that is so attractive for these applications, particularly the resistance of sulfonyl fluorides to hydrolysis under physiological conditions, has provided opportunities for synthetic chemists. New synthetic approaches that start with sulfur-containing substrates include the activation of sulfonamides using pyrilium salts, the deoxygenation of sulfonic acids, and the electrochemical oxidation of thiols. Employing non-sulfur-containing substrates has led to the development of transition-metal-catalysed processes based on palladium, copper and nickel, as well as the use of SO2F2 gas as an electrophilic hub. Selectively manipulating molecules that already contain a sulfonyl fluoride group has also proved to be a popular tactic, with metal-catalysed processes again at the fore. Finally, coaxing sulfonyl fluorides to engage with nucleophiles, when required, and under suitable reaction conditions, has led to new activation methods. This Review provides an overview of the challenges in the efficient synthesis and manipulation of these intriguing functional groups.
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| first_indexed | 2024-03-07T07:14:19Z |
| format | Journal article |
| id | oxford-uuid:c34f767c-0ab6-4c65-aad5-0c96f8fc09b3 |
| institution | University of Oxford |
| language | English |
| last_indexed | 2024-03-07T07:14:19Z |
| publishDate | 2022 |
| publisher | Springer Nature |
| record_format | dspace |
| spelling | oxford-uuid:c34f767c-0ab6-4c65-aad5-0c96f8fc09b32022-07-26T09:45:21ZSulfonyl fluorides as targets and substrates in the development of new synthetic methodsJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:c34f767c-0ab6-4c65-aad5-0c96f8fc09b3EnglishSymplectic ElementsSpringer Nature2022Lou, TS-BWillis, MCThe advent of sulfur(VI)-fluoride exchange (SuFEx) processes as transformations with click-like reactivity has invigorated research into electrophilic species featuring a sulfur–fluorine bond. Among these, sulfonyl fluorides have emerged as the workhorse functional group, with diverse applications being reported. Sulfonyl fluorides are used as electrophilic warheads by both medicinal chemists and chemical biologists. The balance of reactivity and stability that is so attractive for these applications, particularly the resistance of sulfonyl fluorides to hydrolysis under physiological conditions, has provided opportunities for synthetic chemists. New synthetic approaches that start with sulfur-containing substrates include the activation of sulfonamides using pyrilium salts, the deoxygenation of sulfonic acids, and the electrochemical oxidation of thiols. Employing non-sulfur-containing substrates has led to the development of transition-metal-catalysed processes based on palladium, copper and nickel, as well as the use of SO2F2 gas as an electrophilic hub. Selectively manipulating molecules that already contain a sulfonyl fluoride group has also proved to be a popular tactic, with metal-catalysed processes again at the fore. Finally, coaxing sulfonyl fluorides to engage with nucleophiles, when required, and under suitable reaction conditions, has led to new activation methods. This Review provides an overview of the challenges in the efficient synthesis and manipulation of these intriguing functional groups. |
| spellingShingle | Lou, TS-B Willis, MC Sulfonyl fluorides as targets and substrates in the development of new synthetic methods |
| title | Sulfonyl fluorides as targets and substrates in the development of new synthetic methods |
| title_full | Sulfonyl fluorides as targets and substrates in the development of new synthetic methods |
| title_fullStr | Sulfonyl fluorides as targets and substrates in the development of new synthetic methods |
| title_full_unstemmed | Sulfonyl fluorides as targets and substrates in the development of new synthetic methods |
| title_short | Sulfonyl fluorides as targets and substrates in the development of new synthetic methods |
| title_sort | sulfonyl fluorides as targets and substrates in the development of new synthetic methods |
| work_keys_str_mv | AT loutsb sulfonylfluoridesastargetsandsubstratesinthedevelopmentofnewsyntheticmethods AT willismc sulfonylfluoridesastargetsandsubstratesinthedevelopmentofnewsyntheticmethods |