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 …

Click chemistry in the design of AIEgens for biosensing and bioimaging

MC Giel, Y Hong - Aggregate, 2023 - Wiley Online Library
The development of rapid, selective, and sensitive fluorescent sensors is essential for
visualizing and quantifying biological molecules and processes in vitro, ex vitro, and in vivo …

Sulfonyl fluorides (SFs): more than click reagents?

PK Chinthakindi, PI Arvidsson - European Journal of Organic …, 2018 - Wiley Online Library
Sulfonyl fluoride (SF) containing substances are currently attracting enormous attention
among practitioners of both chemical biology and synthetic organic chemistry. The groups of …

Palladium‐Catalyzed Fluorosulfonylvinylation of Organic Iodides

GF Zha, Q Zheng, J Leng, P Wu, HL Qin… - Angewandte Chemie …, 2017 - Wiley Online Library
A palladium‐catalyzed fluorosulfonylvinylation reaction of organic iodides is described.
Catalytic Pd (OAc) 2 with a stoichiometric amount of silver (I) trifluoroacetate enables the …

One-pot fluorosulfurylation of Grignard reagents using sulfuryl fluoride

C Lee, ND Ball, GM Sammis - Chemical Communications, 2019 - pubs.rsc.org
Herein, we report a new method for the one-pot syntheses of sulfonyl fluorides. Addition of
an alkyl, aryl, or heteroaryl Grignard to a solution of sulfuryl fluoride at ambient temperature …

Synthetic strategies for fluorosulfonylated compounds: application to click chemistry reactions

S Barata-Vallejo, DE Yerien, A Postigo - Catalysis Science & …, 2023 - pubs.rsc.org
The syntheses and applications of fluorosulfonylated organic compounds have flourished in
the last ten years due to their versatility to participate in click chemistry (SuFEx) reactions …

The expanding repertoire of covalent warheads for drug discovery

NV Mehta, MS Degani - Drug Discovery Today, 2023 - Elsevier
The reactive functionalities of drugs that engage in covalent interactions with the
enzyme/receptor residue in either a reversible or an irreversible manner are …

A synthesis of “dual warhead” β-aryl ethenesulfonyl fluorides and one-pot reaction to β-sultams

PK Chinthakindi, KB Govender, AS Kumar… - Organic …, 2017 - ACS Publications
Herein, we report an operationally simple, ligand-and additive-free oxidative boron-Heck
coupling that is compatible with the ethenesulfonyl fluoride functional group. The protocol …

Ethenesulfonyl fluoride (ESF) and its derivatives in SuFEx click chemistry and more

YP Meng, SM Wang, WY Fang, ZZ Xie, J Leng… - …, 2020 - thieme-connect.com
The sulfur (VI) fluoride exchange reaction (SuFEx), developed by Sharpless and co-workers
in 2014, is a new category of click reaction that creates molecular connections with absolute …

1-Bromoethene-1-sulfonyl fluoride (1-Br-ESF), a new SuFEx clickable reagent, and its application for regioselective construction of 5-sulfonylfluoro isoxazoles

J Leng, HL Qin - Chemical Communications, 2018 - pubs.rsc.org
A new fluorosulfonylation reagent 1-bromoethene-1-sulfonyl fluoride was developed (1-Br-
ESF). This unique reagent possesses three addressable handles (vinyl, bromide, and …