Linkage chemistry of S (VI) fluorides
D Zeng, WP Deng, X Jiang - Chemistry–A European Journal, 2023 - Wiley Online Library
Sulfur (VI)‐fluoride exchange linkage as a next generation of click chemistry was introduced
by Sharpless and coworkers in 2014. Distinguished from CuAAC, the SuFEx reaction …
by Sharpless and coworkers in 2014. Distinguished from CuAAC, the SuFEx reaction …
Antimicrobial peptides: An alternative to traditional antibiotics
S Ji, F An, T Zhang, M Lou, J Guo, K Liu, Y Zhu… - European Journal of …, 2023 - Elsevier
As antibiotic-resistant bacteria and genes continue to emerge, the identification of effective
alternatives to traditional antibiotics has become a pressing issue. Antimicrobial peptides …
alternatives to traditional antibiotics has become a pressing issue. Antimicrobial peptides …
FSO2N3-Enabled Synthesis of Tetrazoles from Amidines and Guanidines
T Wang, L Xu, J Dong - Organic Letters, 2023 - ACS Publications
Herein we report the facile syntheses of tetrazoles enabled by FSO2N3 under mild
conditions. FSO2N3 has been shown as the most powerful diazotizing reagent, which …
conditions. FSO2N3 has been shown as the most powerful diazotizing reagent, which …
Triazole derivatives as potential antifungal agents: A structure-activity relationship (SAR) studies
Y Hu, Z Liu, G Zha, S Long, MB Sridhara… - Process …, 2023 - Elsevier
Today's research is focused on developing new safe drugs of clinical importance. Nitrogen-
containing heterocycles are abundant in the common of therapeutic scaffolds. Triazoles are …
containing heterocycles are abundant in the common of therapeutic scaffolds. Triazoles are …
Fluorinated azoles as effective weapons in fight against methicillin-resistance staphylococcus aureus (MRSA) and its SAR studies
The rapid spread of Methicillin-resistant Staphylococcus aureus (MRSA) and its difficult-to-
treat skin and filmsy diseases are making MRSA a threat to human life. The most dangerous …
treat skin and filmsy diseases are making MRSA a threat to human life. The most dangerous …
Sulfur-fluoride exchange (SuFEx)-enabled lead discovery of AChE inhibitors by fragment linking strategies
Z Zhang, SL Zhang, C Wu, HH Li, L Zha, J Shi… - European Journal of …, 2023 - Elsevier
SuFEx click chemistry has been a method for the rapid synthesis of functional molecules
with desirable properties. Here, we demonstrated a workflow that allows for in situ synthesis …
with desirable properties. Here, we demonstrated a workflow that allows for in situ synthesis …
The expanding repertoire of covalent warheads for drug discovery
The reactive functionalities of drugs that engage in covalent interactions with the
enzyme/receptor residue in either a reversible or an irreversible manner are …
enzyme/receptor residue in either a reversible or an irreversible manner are …
Click chemistry and targeted degradation: a winning combination for medicinal chemists?
A Pasieka, E Diamanti, E Uliassi… - …, 2023 - Wiley Online Library
Click chemistry is universally recognized as a powerful strategy for the fast and precise
assembly of diverse building blocks. Targeted Protein Degradation (TPD) is a new …
assembly of diverse building blocks. Targeted Protein Degradation (TPD) is a new …
Enantioselective Addition of Dialkyl Malonates to β-Arylethenesulfonyl Fluorides under High-Pressure Conditions
M Kopyt, M Tryniszewski, M Barbasiewicz… - Organic …, 2023 - ACS Publications
Application of high-pressure conditions enables enantioselective Michael-type addition of
dialkyl malonates to β-arylethenesulfonyl fluorides. The reaction is efficiently catalyzed with …
dialkyl malonates to β-arylethenesulfonyl fluorides. The reaction is efficiently catalyzed with …