Regioselective Formal -Allylation of Carbonyl Compounds Enabled by Cooperative Nickel and Photoredox Catalysis

The Tsuji-Trost reaction between carbonyl compounds and allylic precursors has been widely used in the synthesis of natural products and pharmaceutical compounds. As the alpha-C-H bond is far more acidic than the beta-C-H bond, carbonyl compounds undergo highly regioselective allylation at the alpha-position and their beta-allylation is therefore highly challenging. This innate alpha-reactivity conversely hampers diversity, especially if the corresponding beta-allylation product is targeted. Herein, we present a formal intermolecular beta-C-C bond formation reaction of a broad range of aldehydes and ketones with different allyl electrophiles through cooperative nickel and photoredox catalysis. beta-Selectivity is achieved via initial transformation of the aldehydes and ketones to their corresponding silyl enol ethers. The overall transformation features mild conditions, excellent regioselectivity, wide functional group tolerance and high reaction efficiency. The introduced facile and regioselective beta-allylation of carbonyl compounds proceeding through cooperative catalysis allows the preparation of valuable building blocks that are difficult to access from aldehydes and ketones using existing methodology.