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- W4212912078 abstract "Abstract Intermolecular photocatalytic hydroaminoalkylation (HAA) of alkenes have emerged as a powerful method for the construction of alkyl amines. Although there are some studies aiming at stereoselective photocatalytic HAA reactions, the alkenes are limited to electrophilic alkenes. Herein, we report a highly regio‐, diastereo‐, and enantioselective HAA of electron‐rich dienol ethers and α‐amino radicals derived from α‐amino acids using a unified photoredox and palladium catalytic system. This decarboxylative 1,2‐Markovnikov addition enables the construction of vicinal amino tertiary ethers with high levels of regio‐ (up to >19 : 1 rr), diastereo‐ (up to >19 : 1 dr), and enantioselectivity control (up to >99 % ee). Mechanistic studies support a reversible hydropalladation as a key step." @default.
- W4212912078 created "2022-02-24" @default.
- W4212912078 creator A5022567012 @default.
- W4212912078 creator A5048668242 @default.
- W4212912078 creator A5067624195 @default.
- W4212912078 creator A5084409554 @default.
- W4212912078 date "2022-03-16" @default.
- W4212912078 modified "2023-10-05" @default.
- W4212912078 title "Regio‐, Diastereo‐, and Enantioselective Decarboxylative Hydroaminoalkylation of Dienol Ethers Enabled by Dual Palladium/Photoredox Catalysis" @default.
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- W4212912078 doi "https://doi.org/10.1002/ange.202200105" @default.
- W4212912078 hasPublicationYear "2022" @default.
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