Results 11 to 20 of about 5,856 (239)
Copper(II/III) Redox Couple Enables C─H Methylation via a Radical Mechanism Analogous to SAM Enzymes
Biological C–H methylation proceeds through radical pathways mediated by one‐electron redox cofactors, yet no synthetic model has reproduced this reactivity. Here, we report the first isolable Cu(II/III)–methyl complexes that mediate C–H methylation through hydrogen atom transfer and methyl radical rebound.
Emily N. Doss +2 more
wiley +2 more sources
Re‐envisioning the Ligandable Proteome: Reactive Metallo‐Scaffolds (r‐mS) combine non‐covalent protein engagement by a metallo‐scaffold with covalent cysteine capture through a tethered chloroacetamide warhead. Chemoproteomic profiling reveals unique enzyme engagement including ligases, kinases and methyltransferases, highlighting opportunities for ...
Jessica E. Waters +15 more
wiley +2 more sources
A Catalytic Osmium Redox Couple Collapses Cancer Redox Balance
A stable Os(III)/Os(IV) redox couple is developed to disrupt the tumor cell redox balance by concurrently catalyzing ROS generation and GSH depletion. Osmium‐treated cells exhibit multiple cell death pathways, including apoptosis, ferroptosis, and immunogenic cell death.
Wan‐Qiong Huang +9 more
wiley +1 more source
Mechanistic Understanding of Protein–MOF Integration Through Surfactant‐Driven Interfacial Design
This study reveals how surfactant‐driven interfacial design governs the assembly and stability of protein@MOF composites. Using lipid‐based nonionic surfactants, we modulate protein–MOF interactions to improve encapsulation efficiency, MOF crystallization, and catalytic performance.
Ehsan Rashidniyaghi +4 more
wiley +1 more source
Gold(I) Phosphine/Phosphido‐Borohydride Complexes
Synthesis, structure, and electrochemical characteristics of a homologous series of gold(I) complexes featuring phosphine and phosphido–borohydride ligands. A homologous series of linear, mononuclear gold(I) phosphine/phosphido‐borohydride complexes, encompassing [Au(PR3)2]+ 1, [Au(PR3)(PR2BH3)] 2 and [Au(PR2BH3)2]– 3 (R = tBu, Ad), has been prepared ...
Matthew J. G. Sinclair +3 more
wiley +1 more source
On Oxalyl Halide Isothiocyanates Part II: Decarbonylation and Reactivity Studies
Thermal decarbonylation of oxalyl halide isothiocyanates affords the respective carbonyl halide isothiocyanates as liquids. Crystals grown from melt allowed the elucidation of their crystal structures. Spectroscopic signatures (IR, Raman, NMR) are presented alongside reactivity studies. The reaction of oxalyl halide isothiocyanate, X(CO)2NCS (X = Cl (1)
Sven Ringelband, Frank Tambornino
wiley +1 more source
On Oxalyl Halide Isothiocyanates Part I: Syntheses and Isomerism
Oxalyl halide isothiocyanates can be prepared from oxalyl halide with one equivalent of NH4SCN in liquid SO2. While oxalyl bromide isothiocyanate can be isolated as a liquid, the respective chloride compound readily undergoes isomerization under formation of a thiazole ring, which is obtained as a solid.
Sven Ringelband +2 more
wiley +1 more source
Hydrosilane Chemistry: From Historic First Steps to Modern Applications
This review covers the history of hydrosilanes, from their initial discovery to their modern applications. It highlights the pioneering work of chemists like Alfred Stock and Franz Fehér and discusses the modern ways of synthesis and use of hydrosilanes in printed electronics.
Uwe Böhme, Maik Gerwig
wiley +1 more source
Upon reduction of 1,4‐diaza‐1,3‐diene 1 to the dilithium enediamide 2, the polarity of the C = N bonds is reversed ‐ a classic case of umpolung. This behavior is particularly evident in reactions of the dianion 2 with carbonyl compounds and also explains why 1,4‐diaza‐1,3‐diene ligands do not always act merely as spectator ligands. 1,4‐Diaza‐1,3‐dienes
Muhan Liang +3 more
wiley +1 more source
Carbon Dioxide Insertion by a Methylene‐Bridged Ga/P FLP
In a salt elimination of Bis2GaBr (Bis = CH(SiMe3)2) with LiCH2PtBu2 the Bis2Ga–CH2–PtBu2 frustrated Lewis pairs is afforded. While forming usual 1,2‐adducts with cis‐azobenzene, CS2 and CO2, the latter shows an exceptional insertion when heated to 70°C, leading to a gallium carboxylate.
Julian Buth +4 more
wiley +1 more source

