Chemical and biology of sulfur fluoride exchange (SuFEx) click chemistry for drug discovery
Compounds containing an Ssingle bondF bond have garnered intense interest in the
chemical and biological literature. In particular, sulfonyl fluorides (RSO 2 F) are commonly …
chemical and biological literature. In particular, sulfonyl fluorides (RSO 2 F) are commonly …
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 …
Fluorochemicals from fluorspar via a phosphate-enabled mechanochemical process that bypasses HF
C Patel, E André-Joyaux, JA Leitch… - Science, 2023 - science.org
All fluorochemicals—including elemental fluorine and nucleophilic, electrophilic, and radical
fluorinating reagents—are prepared from hydrogen fluoride (HF). This highly toxic and …
fluorinating reagents—are prepared from hydrogen fluoride (HF). This highly toxic and …
Direct mapping of ligandable tyrosines and lysines in cells with chiral sulfonyl fluoride probes
Advances in chemoproteomic technology have revealed covalent interactions between
small molecules and protein nucleophiles, primarily cysteine, on a proteome-wide scale …
small molecules and protein nucleophiles, primarily cysteine, on a proteome-wide scale …
Photoredox Catalysis-Enabled Sulfination of Alcohols and Bromides
WP Carson II, PJ Sarver, NS Goudy… - Journal of the …, 2023 - ACS Publications
Sulfinates are important lynchpin intermediates in pharmaceutical production; however, their
synthesis via photoredox catalysis is challenging because of their facile oxidation. We …
synthesis via photoredox catalysis is challenging because of their facile oxidation. We …
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 …
Turning sulfonyl and sulfonimidoyl fluoride electrophiles into sulfur (VI) radicals for alkene ligation
X Wu, W Zhang, G Sun, X Zou, X Sang, Y He… - Nature …, 2023 - nature.com
Sulfonyl and sulfonimidoyl fluorides are versatile substrates in organic synthesis and
medicinal chemistry. However, they have been exclusively used as S (VI)+ electrophiles for …
medicinal chemistry. However, they have been exclusively used as S (VI)+ electrophiles for …
Electroreductive hydroxy fluorosulfonylation of alkenes
Q Feng, T He, S Qian, P Xu, S Liao, S Huang - Nature Communications, 2023 - nature.com
An electroreductive strategy for radical hydroxyl fluorosulfonylation of alkenes with sulfuryl
chlorofluoride and molecular oxygen from air is described. This mild protocol displays …
chlorofluoride and molecular oxygen from air is described. This mild protocol displays …
Sulfur (VI) fluorides as tools in biomolecular and medicinal chemistry
SN Carneiro, SR Khasnavis, J Lee, TW Butler… - Organic & …, 2023 - pubs.rsc.org
Recent advances in the synthesis of sulfur (VI)-fluorides has enabled incredible growth in
their application in biomolecular chemistry. This review aims to serve as a primer …
their application in biomolecular chemistry. This review aims to serve as a primer …