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 …
like reactivity has invigorated research into electrophilic species featuring a sulfur–fluorine …
Synthesis of sulfonamide and their synthetic and therapeutic applications: Recent advances
S Mondal, S Malakar - Tetrahedron, 2020 - Elsevier
A sulfonamide is a functional group that is the basis of several sulfa drugs and thereby are
very much important scaffolds in medicinal as well as in synthetic organic chemistry …
very much important scaffolds in medicinal as well as in synthetic organic chemistry …
EnT-mediated N–S bond homolysis of a bifunctional reagent leading to aliphatic sulfonyl fluorides
JE Erchinger, R Hoogesteger, R Laskar… - Journal of the …, 2023 - ACS Publications
Sulfur (VI) fluoride exchange (SuFEx) gives rise to a plethora of high-valent sulfur linkages;
however, the availability of (aliphatic) sulfonyl fluoride manifolds lag behind, owing to the …
however, the availability of (aliphatic) sulfonyl fluoride manifolds lag behind, owing to the …
Scalable, Chemoselective Nickel Electrocatalytic Sulfinylation of Aryl Halides with SO2
TSB Lou, Y Kawamata, T Ewing… - Angewandte Chemie …, 2022 - Wiley Online Library
Simple access to aryl sulfinates from aryl iodides and bromides is reported using an
inexpensive Ni‐electrocatalytic protocol. The reaction exhibits a broad scope, uses stock …
inexpensive Ni‐electrocatalytic protocol. The reaction exhibits a broad scope, uses stock …
The emerging applications of sulfur (VI) fluorides in catalysis
C Lee, AJ Cook, JE Elisabeth, NC Friede… - ACS …, 2021 - ACS Publications
The past decade has witnessed remarkable growth of catalytic transformations in organic
sulfur (VI) fluoride chemistry. This Perspective concentrates exclusively on foundational …
sulfur (VI) fluoride chemistry. This Perspective concentrates exclusively on foundational …
Radical Hydro‐Fluorosulfonylation of Unactivated Alkenes and Alkynes
P Wang, H Zhang, M Zhao, S Ji, L Lin… - Angewandte Chemie …, 2022 - Wiley Online Library
Recently, radical fluorosulfonylation is emerging as an appealing approach for the synthesis
of sulfonyl fluorides, which are highly in demand in various disciplines, particularly in …
of sulfonyl fluorides, which are highly in demand in various disciplines, particularly in …
A practical fluorosulfonylating platform via photocatalytic imidazolium-based SO2F radical reagent
W Zhang, H Li, X Li, Z Zou, M Huang, J Liu… - Nature …, 2022 - nature.com
Sulfonyl fluorides are key components in the fields of chemical biology, materials science
and drug discovery. In this line, the highly active SO2F radical has been employed for the …
and drug discovery. In this line, the highly active SO2F radical has been employed for the …
The same oxygenation-state introduction of hypervalent sulfur under transition-metal-free conditions
D Zeng, M Wang, WP Deng, X Jiang - Organic Chemistry Frontiers, 2020 - pubs.rsc.org
Sulfonyl compounds have attracted considerable interest due to their extensive applications
in drug discovery. Access to the assembly of SO2-containing compounds via the …
in drug discovery. Access to the assembly of SO2-containing compounds via the …
Redox-neutral organometallic elementary steps at bismuth: catalytic synthesis of aryl sulfonyl fluorides
M Magre, J Cornella - Journal of the American Chemical Society, 2021 - ACS Publications
A Bi-catalyzed synthesis of sulfonyl fluorides from the corresponding (hetero) aryl boronic
acids is presented. We demonstrate that the organobismuth (III) catalysts bearing a bis-aryl …
acids is presented. We demonstrate that the organobismuth (III) catalysts bearing a bis-aryl …
Selective fluorosulfonylation of thianthrenium salts enabled by electrochemistry
X Kong, Y Chen, Q Liu, WJ Wang, S Zhang… - Organic …, 2023 - ACS Publications
A practical electrochemically driven method for fluorosulfonylation of both aryl and alkyl
thianthrenium salts has been disclosed. The strategy does not need external redox reagents …
thianthrenium salts has been disclosed. The strategy does not need external redox reagents …