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- W4377087984 abstract "Dual photoredox–transition-metal catalysis has emerged as a powerful tool for the development of chemical transformations. However, its application in the selective difunctionalization of 1,3-dienes remains essentially unexploited. By the synergistic action of photoredox and copper catalysts, we report herein an enantioselective 1,2-amidocyanation of 1,3-dienes. Visible-light irradiation of a chloroform solution of conjugated dienes, N-Boc-amidopyridinium salts, and TMSCN in the presence of a catalytic amount of fac-Ir(ppy)3, Cu(OTf)2·xH2O, and a chiral Box ligand affords three-component adducts in good to high yields with high regio- and enantioselectivities. A L*CuCN complex, fully characterized spectroscopically and confirmed by X-ray crystallographic analysis, is able to catalyze the transformation, therefore supporting an inner-sphere cyanide transfer pathway." @default.
- W4377087984 created "2023-05-20" @default.
- W4377087984 creator A5034016630 @default.
- W4377087984 creator A5046323119 @default.
- W4377087984 creator A5055586375 @default.
- W4377087984 creator A5091978899 @default.
- W4377087984 date "2023-05-19" @default.
- W4377087984 modified "2023-10-05" @default.
- W4377087984 title "Dual Photoredox and Copper Catalysis: Enantioselective 1,2-Amidocyanation of 1,3-Dienes" @default.
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- W4377087984 doi "https://doi.org/10.1021/acscatal.3c01782" @default.
- W4377087984 hasPublicationYear "2023" @default.
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