Development of one-pot benzylic amination reactions of azine N-oxides
Embargo Lift Date: 2020-05-02
Türkmen, Y. E.
0040-4039 (print)1873-3581 (online)
1723 - 1727
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An efficient one-pot synthetic methodology has been developed for the benzylic amination reactions of methyl-substituted azine N-oxides that operate under mild conditions. The reaction was found to tolerate quinoline and isoquinoline N-oxides with electron donating and withdrawing substituents as the electrophilic reaction partners as well as a broad range of nucleophilic primary, secondary and aromatic amines, affording the benzylic amination products in up to 82% yield.