Photocatalytic carbocarboxylation of styrenes with CO2 for the synthesis of γ-aminobutyric esters

Abstract

Metal-free photoredox-catalyzed carbocarboxylation of various styrenes with carbon dioxide (CO₂) and amines to obtain γ-aminobutyric ester derivatives has been developed (up to 91% yield, 36 examples). The radical anion of (2,3,4,6)-3-benzyl-2,4,5,6-tetra(9H-carbazol-9-yl)benzonitrile (4CzBnBN) possessing a high reduction potential (−1.72 V vs. saturated calomel electrode (SCE)) easily reduces both electron-donating and electron-withdrawing group-substituted styrenes.