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- W3197685943 endingPage "8585" @default.
- W3197685943 startingPage "8578" @default.
- W3197685943 abstract "Allylamines are versatile building blocks in the synthesis of various naturally occurring products and pharmaceuticals. In contrast to terminal allylamines, the methods of synthesis of their branched congeners with internal, stereodefined double bonds are less explored. This work describes a new approach for the preparation of allylamines via cross-coupling of alkyl bromides with simple 3-bromoallylamines by merging the photoredox approach and Ni catalysis. The reaction proceeds under mild conditions, under blue light irradiation, and in the presence of an organic dye, 4CzIPN, as a photocatalyst. The scope of suitable reaction partners is broad, including alkyl bromides bearing reactive functionalities (e.g., esters, nitriles, aldehydes, ketones, epoxides) and N-protected allylamines, as well as N-allylated secondary and tertiary amines and heterocycles. The employment of non-racemic starting materials allows for rapid and easy construction of complex multifunctional allylamine derivatives without the loss of enantiomeric purity." @default.
- W3197685943 created "2021-09-13" @default.
- W3197685943 creator A5047468950 @default.
- W3197685943 creator A5018671619 @default.
- W3197685943 date "2021-01-01" @default.
- W3197685943 modified "2023-09-24" @default.
- W3197685943 title "Synthesis of chiral branched allylamines through dual photoredox/nickel catalysis" @default.
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