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- W3154392004 abstract "A three-component 1,2-aminoarylation of vinyl ethers, enamides, ene-carbamates and vinyl thioethers by synergistic photoredox and nickel catalysis is reported. 2,2,2-Trifluoroethoxy carbonyl protected α-amino-oxy acids are used as amidyl radical precursors. anti-Markovnikov addition of the amidyl radical to the alkene and Ni-mediated radical/transition metal cross over lead to the corresponding 1,2-aminoarylation product. The radical cascade, which can be conducted under practical and mild conditions, features high functional group tolerance and broad substrate scope. Stereoselective 1,2-aminoarylation is achieved using a L-(+)-lactic acid derived vinyl ether as the substrate, offering a novel route for the preparation of protected enantiopure α-arylated β-amino alcohols. In addition, 1,2-aminoacylation of vinyl ethers is achieved by using an acyl succinimide as the electrophile for the Ni-mediated radical coupling." @default.
- W3154392004 created "2021-04-26" @default.
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- W3154392004 date "2021-05-19" @default.
- W3154392004 modified "2023-10-17" @default.
- W3154392004 title "Three‐Component Aminoarylation of Electron‐Rich Alkenes by Merging Photoredox with Nickel Catalysis" @default.
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- W3154392004 doi "https://doi.org/10.1002/anie.202101775" @default.
- W3154392004 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/8252614" @default.
- W3154392004 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/33871137" @default.
- W3154392004 hasPublicationYear "2021" @default.
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