Catalytic allylic functionalization via π-allyl palladium chemistry

Organic & Biomolecular Chemistry Pub Date: 2019-09-16 DOI: 10.1039/C9OB01725A

Abstract

This review highlights the developments in palladium-catalyzed allylic C–H functionalization from early 2014 to the present date. π-Allylpalladium chemistry emphasizes the research originating from less appealing stoichiometric Pd(II) based allylic C–H activation to the present day green, step- and atom-economical and sustainable strategy, wherein the allylic hydrogen atom becomes the “l(fā)eaving group”. This constitutes a direct C–H activation method, which is essentially catalytic in the presence of a terminal oxidant to regenerate the Pd(II)-species from Pd(0). The availability of chiral ligands, under oxidative conditions, has paved the way to realize asymmetric oxidative Tsuji–Trost allylic alkylations.

Graphical abstract: Catalytic allylic functionalization via π-allyl palladium chemistry
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