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Enzymatic Cascade Reactions for the Synthesis of Chiral Amino Alcohols from L-lysine
Published on: February 16, 2018
Enantioselective Reductive Alkenylation of α-CF2H (-CF3) Amino Halides: Rapid Access to Chiral α-CF2H (-CF3)
Peng Liu1,2, Kuiliang Li3, Yan He2
1Department of Pharmacy, Division of Life Sciences and Medicine, The First Affiliated Hospital of USTC, University of Science and Technology of China, Hefei, China.
Abstract:
The incorporation of fluoroalkyl groups into drug candidates has garnered increasing attention in the pharmaceutical industry due to their ability to modulate lipophilicity, permeability, metabolic stability, and binding affinity. Despite significant advances realized, the means to introducing fluoroalkyl groups such as ─CF2H or ─CF3 in an enantioselective manner remain scarce. Herein, we report a Ni-catalyzed enantioselective reductive alkenylation of α-CF2H or ─CF3 amino chlorides with vinyl iodides. This method provides an efficient and modular technique for constructing stereocenters bearing a fluoroalkyl group. A key to success was the incorporation of an arylamide moiety with the substrates, which stabilizes the α-fluoroalkyl radical intermediate, thus offering a de novo approach to access enantioenriched α-CF2H (─CF3) allylamines. Our protocol is characterized by its mild reaction conditions, broad substrate scope, as well as excellent enantio-and chemo-selectivity, even in the context of late-stage functionalization.
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