115974-95-3Relevant articles and documents
Aryldiazonium silica sulfates as efficient reagents for Heck-type arylation reactions under mild conditions
Zarei, Amin,Khazdooz, Leila,Pirisedigh, Azadeh,Hajipour, Abdol R.,Seyedjamali, Hojjat,Aghaei, Hamidreza
, p. 4554 - 4557 (2011)
An efficient and straightforward procedure for Heck-type arylation reactions was studied using aryldiazonium silica sulfates and olefins in the presence of a catalytic amount of Pd(OAc)2. These reactions were carried out in water at room temperature without using a base or additional ligands. The use of a non-toxic solvent, a simple and clean work-up, short reaction times, and good yields are advantages of this method.
Regioselective organocatalyzed asymmetric bromolactonization of aryl acrylate-type carboxylic acids: a new approach towards enantioenriched 3-substituted isobenzofuranones
Gelat, Fabien,Coffinet, Micha?l,Lebrun, Stéphane,Agbossou-Niedercorn, Francine,Michon, Christophe,Deniau, Eric
, p. 980 - 989 (2016/09/13)
The enantioselective synthesis of several 3-substituted isobenzofuranones has been developed through a new and flexible route. When combined with a catalytic amount of benzoic acid, quinidine thiocarbamate bifunctional catalysts have demonstrated their efficiency for the highly regioselective organocatalyzed asymmetric bromolactonization reaction of aryl acrylate-type carboxylic acids.
Synthesis of isoindolinones via palladium-catalyzed C-H activation of N-methoxybenzamides
Li, Dan-Dan,Yuan, Ting-Ting,Wang, Guan-Wu
supporting information; experimental part, p. 12789 - 12791 (2012/01/05)
The synthesis of isoindolinones from N-methoxybenzamides and alkenes has been achieved by Pd-catalyzed ortho sp2 C-H activation and intramolecular oxidative amidation, which involve the cleavage of four bonds and formation of two bonds.
