Qingzong Wang

TL;DR: A palladium-catalyzed addition of potassium aryltrifluoroborates to aliphatic nitriles has been developed, leading to a wide range of alkyl aries ketones with moderate to excellent yields and is applicable to library synthesis.

TL;DR: A palladium-catalyzed tandem addition/cyclization of 2-(2-aminoaryl)acetonitriles with arylboronic acids with halogen substituents has been developed for the first time, achieving a new strategy for direct construction of indole skeletons.

TL;DR: A palladium-catalyzed addition of potassium aryltrifluoroborates to aliphatic nitriles has been developed, leading to a wide range of alkyl aryls ketones with moderate to excellent yields as mentioned in this paper.

TL;DR: In this paper, a method for compounding an amino-substituted arylate compound is described. But the method comprises the step that under the condition of the adoption of a copper source compound catalyst and a ligand, and isatoic anhydride derivative and organic cyclic borate compound react in an organic solvent, so that the decarboxylation coupling reaction of isatoically anhydrides is realized, high-yield and high-purity amino-saturated aryl compound is obtained, a new compounding way is

TL;DR: The scope of the developed approach was successfully explored toward the addition of potassium phenyltrifluoroborate to aromatic dinitriles in 2-MeTHF, achieving diphenyl diones in moderate to excellent yields.