103681-94-3Relevant articles and documents
Directed: Ortho-metalation-nucleophilic acyl substitution strategies in deep eutectic solvents: The organolithium base dictates the chemoselectivity
Ghinato, Simone,Dilauro, Giuseppe,Perna, Filippo Maria,Capriati, Vito,Blangetti, Marco,Prandi, Cristina
, p. 7741 - 7744 (2019/07/12)
Directed ortho metalation (DoM) or nucleophilic acyl substitution (SNAc) can be efficiently programmed on the same aromatic carboxylic acid amide, in a choline chloride-based eutectic mixture, by simply switching the nature of the organolithium reagent. Telescoped, one-pot ortho-lithiation/Suzuki-Miyaura cross-couplings have also been demonstrated for the first time in Deep Eutectic Solvents.
SYNTHETIC CONNECTIONS TO THE AROMATIC DIRECTED METALATION REACTION. UNSYMMETRICAL BIARYLS BY PALLADIUM-CATALYZED CROSS COUPLING OF DIRECTED METALATION-DERIVED ARYLBORONIC ACIDS WITH ARYL HALIDES
Sharp, M.J.,Snieckus, V.
, p. 5997 - 6000 (2007/10/02)
The arylboronic acids 2 and 4 derived by directed ortho metalation of benzamides and carbamates, undergo an efficient palladium-catalyzed cross coupling reaction with a variety of aryl halides to yield unsymmetrical biaryls and heterobiaryls (Table).