Weike Su

TL;DR: A palladium-catalyzed aromatic esterification reaction of aldehydes with arylboronic acids under an air atmosphere was achieved in this paper, where the reaction tolerates many functional groups and provides aryls benzoate derivatives with yields ranging from moderate to good.

TL;DR: Aryl- or hetero-boronic acids with aldehydes, in the presence of PdCl2 and P(1-Nap)3, afforded carbinol derivatives in good to excellent yields.

TL;DR: In this paper, a method for synthesizing quinazolinone compounds using trifluoro mesylate as a catalyst is described. But the method is not suitable for high reaction yield up to more than 85 percent generally, advanced and reasonable process routes, mild reaction conditions, little dosage of the catalyst, reutilization and substantially no three wastes.

TL;DR: In this article, various aldehydes and aldimines undergo a reformatsky reaction mediated by non-activated indium at room temperature to give the corresponding esters in good to excellent yields.