1027335-58-5Relevant academic research and scientific papers
Mechanistic insight into direct arylations with ruthenium(II) carboxylate catalysts
Ackermann, Lutz,Vicente, Ruben,Potukuchi, Harish K.,Pirovano, Valentina
supporting information; experimental part, p. 5032 - 5035 (2010/12/25)
Mechanistic studies revealed ruthenium-catalyzed direct arylations to proceed through reversible C-H bond activation and subsequent rate-limiting oxidative addition with aryl halides, which led to the development of widely applicable well-defined rutheniu
Catalytic direct arylations in polyethylene glycol (PEG): Recyclable palladium(O) catalyst for C-H bond cleavages in the presence of air
Ackermann, Lutz,Vicente, Ruben
supporting information; experimental part, p. 4922 - 4925 (2010/01/16)
Two protocols for ruthenium- or palladium-catalyzed direct arylations In user-friendly polyethylene glycol (PEG) were devised, which set the stage for the development of user-friendly paliadium(0)-cataiyzed C-H bond functionalizations In the presence of a
Assisted ruthenium-catalyzed C-H bond activation: Carboxylic acids as cocatalysts for generally applicable direct arylations in apolar solvents
Ackermann, Lutz,Vicente, Ruben,Althammer, Andreas
supporting information; experimental part, p. 2299 - 2302 (2009/05/11)
(Chemical Equation Presented) Catalytic amounts of aromatic carboxylic acid MesCO2H enabled efficient ruthenium-catalyzed direct arylations in apolar solvents with unparalleled broad scope via a concerted deprotonation-metalation mechanism.
