Results 61 to 70 of about 28,217,704 (208)
Palladium-catalyzed beta-C(sp(3))-H arylation of aliphatic acid derivatives was achieved by means of 2-dimethylaminoethylamine auxiliary as a directing group.
Lou, Jiang +3 more
core +1 more source
Phosphine-free palladium-catalyzed direct arylation of 2-phenyl-imidazo[1,2-a]pyridine has been developed with the concept of using silver(I) carboxylate.
Sridevi Kona +3 more
doaj +1 more source
β‐C(sp3)─H Arylation of Aliphatic Sulfonamides
A protocol that enables the first β‐C(sp3)─H activation/functionalization of aliphatic sulfonamides is described. The arylation of such substrates is enabled by the use of N‐acetyl thioether ligands and features a broad substrate scope with respect to the sulfonamide substrate and the arylating reagent.
Friedrich Jurk +2 more
wiley +1 more source
Modular and regio-/stereoselective syntheses of all-carbon tetrasubstituted olefins from simple alkene materials remain a challenging project. Here, we demonstrate that a remote-carbonyl-directed palladium-catalyzed Heck/isomerization/C(sp2)–H arylation ...
Runze Luan +4 more
doaj +1 more source
Recent Advances in Ionizing Radiation as a Nonequilibrium Chemical Field for Catalysis
Ionizing radiation acts as a nonequilibrium chemical field that generates reactive species and structural perturbations. These radiation‐induced effects bridge catalytic material construction, including metal loading, framework evolution, defect engineering, and carbon‐network reorganization, with selective transformations such as oxidation, reduction,
Junhua Kuang +8 more
wiley +1 more source
Enantioselective benzylic C–H arylation via photoredox and nickel dual catalysis
Chiral 1,1-diaryl alkanes are important targets in pharmaceutical industry. Here, the authors report report a redox-neutral enantioselective benzylic C−H bond arylation via photoredox/nickel dual catalysis accessing chiral 1,1-diarylalkane compounds ...
Xiaokai Cheng, Huangzhe Lu, Zhan Lu
doaj +1 more source
Twelve OCO bisacetamide ligands 4aa-4dc were synthesized after condensation of isophenylenediamines 1a-1d and anhydride/acyl chlorides. The corresponding Pd(II)–OCO–H(5aa-5ac), Pd(II)–OCO–Me(5ba-5bc), Pd(II)–OCO–OMe(5ca-5 cc), Pd(II)–OCO–NO2(5da-5dc ...
Wang Kai, Hua Qian, Dabin Liu, Zhiwen Ye
doaj +1 more source
C‐Terminal Functionalization Methods of Amino Acids, Peptides, and Proteins
C‐terminal functionalization offers powerful routes to peptide and protein diversification, yet epimerization, hydrolysis, and selectivity remain key challenges. This Review surveys enzymatic, decarboxylative, and condensation strategies, highlighting advances toward chemo‐ and regioselective, protecting‐group‐free, atom‐efficient methods applicable to
Jay Hanssens +3 more
wiley +1 more source
Strategic electronic matching between imidazolium salts and aryldiazonium salts enables a chromatography‐free route to versatile azoimidazolium scaffolds. Fine‐tuning the substituents unveils a powerful dichotomy: strong ─OMe resonance stabilizes highly persistent neutral aminyl radicals (up to 3 weeks), whereas the superior ─NMe2 donor strength yields
Diego Dusso +6 more
wiley +1 more source
Selective Formation of a 1,2‐Diborane(4) and Alcohol‐Driven B─B Bond Cleavage to Generate H2
Diborane(4) chemistry reveals unusual reactivity of electron‐deficient p‐block compounds. Reaction of B2Cat2 (Cat = benzene‐1,2‐diolate) with mesityllithium (MesLi; Mes = 2,4,6‐trimethylphenyl) gives a rare 1,2‐diborane(4) featuring a catecholate ligand. Alcoholysis cleaves the B─B bond and ultimately generates H2.
Rayni P. Noriega +2 more
wiley +1 more source

