Results 101 to 110 of about 11,349 (193)
Boronic Acid Inhibitors of β‐Lactamases: A Promising Strategy Against Antimicrobial Resistance
ABSTRACT The rise of antimicrobial resistance (AMR) poses a critical threat to global health, mostly due to the proliferation of β‐lactamases, a class of enzymes responsible for the inactivation of β‐lactam antibiotics. Among the most promising strategies to restore β‐lactam efficacy is the use of β‐lactamase inhibitors (BLIs), with boronic acid ...
Nicolò Santi +4 more
wiley +1 more source
Extent of the Oxidative Side Reactions to Peptides and Proteins During the CuAAC Reaction
The copper-catalyzed azide–alkyne cycloaddition (CuAAC) reaction is a powerful tool for bioconjugation of biomolecules, particularly proteins and peptides.
Honghao Cai (510333) +8 more
core +1 more source
Three ferrocene‐BODIPY‐C60‐peptides (T1–T3) were synthesized and grafted on gold surfaces to form self‐assembled monolayers. Calculation of the tilt angles and surface density of these SAMs using PM‐IRRAS and ultrafast electrochemical experiments revealed that less vertically oriented and densely packed monolayers were obtained compared with previously
Jad Rabah +8 more
wiley +1 more source
Naphthalene diimide (NDI) cores with peripheral fluorocyclohexyl ring systems are explored binding to G‐quadruplex DNA and were also assayed against the Trypanosoma brucei parasite. The most active compound of the series displayed nanomolar activity and suggested electrostatic interactions between the polarized cyclohexane and G‐Quad DNA.
Josephine M. Stewart +7 more
wiley +1 more source
Modulating catalytic activity of polymer-based cuAAC "click" reactions
The copper(I)-catalyzed azide-alkyne cycloaddition (CuAAC) reaction is used to synthesize complex polymer architectures. In this work, we demonstrate the control of this reaction at 25 degrees C between polystyrene (PSTY) chains through modulating the ...
Jia, Zhongfan +7 more
core +1 more source
Thiolane sulfoximines provide practical and safer surrogates for hazardous azides in nitrene photochemistry, enabling direct access to 7,8‐diaminoquinolines and fused δ‐lactams. DFT calculations support the reaction mechanism and rationalize product selectivity.
Lorenzo Serusi +5 more
wiley +1 more source
Safirinium Fluorescent “Click” Molecular Probes: Synthesis, CuAAC Reactions, and Microscopic Imaging
Fluorescent labeling utilizing Cu(I)-catalyzed azide–alkyne cycloaddition reactions (CuAAC) is among the leading applications of the “click” chemistry strategy.
Patryk Kasza +10 more
doaj +1 more source
‐lactide) copolymers by CuAAC click chemistry
Altinkok, Cagatay (Trakya author)The syntheses of polypropylene-graft-poly(l-lactide) copolymers (PP-g-PLAs) via copper (I)-catalyzed azide-alkyne cycloaddition "click" reaction (CuAAC) using azide side-chain functionalized polypropylene (PP-N-3) and ...
Mehmet Atilla Tasdelen +5 more
core +1 more source
Strain and Chirality: Catalytic Asymmetric Synthesis of Planar Chiral [2.2]Paracyclophanes
Catalytic asymmetric synthesis is transforming access to planar‐chiral [2.2]paracyclophanes. This Review highlights recent advances in catalytic desymmetrization and asymmetric functionalization, emphasizing how catalyst design and PCP geometry govern reactivity and stereocontrol.
Daniel Alonso +2 more
wiley +1 more source
Redox‐Active Verdazyl Radical Polymers via Postpolymerization Modification of Active Ester Polymers
Organic radical polymers were synthesized via postpolymerization modification (PPM) of poly(pentafluorophenyl (meth)acrylate) with diverse 6‐oxoverdazyl stable radicals. This work servs as an electrochemical proof‐of‐concept, exhibiting a chemically reversible redox couple at 3.43 V versus Li/Li+, validating the electrochemical accessibility of the ...
Theo A. Ellingsen +7 more
wiley +1 more source

