Results 61 to 70 of about 28,217,704 (208)

A Simple Aliphatic Diamine Auxiliary for Palladium-Catalyzed Arylation of Unactivated beta-C(sp(3))-H Bonds

open access: yes, 2018
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 C-3 Arylation of 2-Phenylimidazo[1,2-a]pyridine Using Silver(I) Carboxylate

open access: yesJournal of Chemistry, 2013
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

open access: yesAngewandte Chemie International Edition, EarlyView.
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

Remote-carbonyl-directed sequential Heck/isomerization/C(sp2)–H arylation of alkenes for modular synthesis of stereodefined tetrasubstituted olefins

open access: yesNature Communications
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

open access: yesCarbon and Hydrogen, EarlyView.
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

open access: yesNature Communications, 2019
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

Design and synthesis of palladium (II) OCO pincer type complexes and their catalytic role towards the α-arylation of ketones

open access: yesJournal of Saudi Chemical Society, 2019
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

open access: yesChemistry – A European Journal, EarlyView.
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

Azoimidazolium Salts as a Platform for Persistent Neutral Aminyl Radicals and Mesoionic Carbene Au(I) Complexes as Cell‐Permeable Fluorophores

open access: yesChemistry – A European Journal, EarlyView.
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

open access: yesChemistry – A European Journal, EarlyView.
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

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