Litcius/Paper detail

Solvent-Controlled Enantioselective Allylic C–H Alkylation of 2,5-Dihydrofuran via Synergistic Palladium/Nickel Catalysis

Fule Wu, Hongkai Wang, Zhenwei Wu, Yangbin Liu, Xiaoming Feng

2025Journal of the American Chemical Society11 citationsDOI

Abstract

Enantioenriched, substituted tetrahydrofuran skeletons extensively occur in natural products, bioactive targets, and organic frameworks. The rapid and diverse synthesis of these tetrahydrofuran molecules is highly desired yet challenging. Herein, we present a practical synthetic strategy for asymmetric allylic C–H bond functionalization of oxyheterocyclic alkenes by making use of the synergistic catalysis of achiral Pd complex and chiral N, N ′-dioxide-Ni(II) catalyst. Notably, the chemodivergent synthesis of allylic C–H alkylated products and hydroalkylated products was readily achieved in good outcomes via the regulation of solvents. Furthermore, the post-transformation of these functionalized 2,5-dihydrofurans provides an innovative synthetic route to access tetrahydrofuran skeleton compounds containing multiple stereocenters.

Topics & Concepts

ChemistryTetrahydrofuranTsuji–Trost reactionEnantioselective synthesisStereocenterAllylic rearrangementPalladiumCatalysisAlkylationCombinatorial chemistryOrganic chemistrySolventCatalytic C–H Functionalization MethodsAlkaloids: synthesis and pharmacologyTraditional and Medicinal Uses of Annonaceae