Abstract
A H4SiW12O40-catalyzed three-component tandem reaction of 2-acylbenzoic acids,primary amines and phosphine oxides to form 3,3-disubstituted isoindolinones was developed.By employing H4SiW12O40 as the catalyst and dimethyl carbonate(DMC)as the solvent,a diverse range of 2-acylbenzoic acid deriva-tives and primary amines worked well to give the C3-phosphinoyl-functionalized 3,3-disubstituted isoin-dolinones with the yield range of 61%-87%.Advantages of this transformation include green catalyst and solvent,available starting materials,broad substrate scope,high efficiency and operational simplicity with water as the sole by-product.The strategy achieved an efficient and green molecular fragment assembly to access isoindolinones,which would provide opportunities for the synthesis of potential biologically active molecules in a green manner.
基金项目
国家自然科学基金(22001034)
江西省自然科学基金(20212BAB213001)