Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5217438 | Tetrahedron | 2013 | 7 Pages |
Abstract
3-Chloropiperidine compounds were obtained via Cu(II)-promoted one-pot intramolecular chloroamination of N-benzyl-4-penten-1-amines and subsequent rearrangement. The reaction conditions leading to this skeleton were studied, and the structure of the product was confirmed by NMR as well as X-ray diffraction experiments.
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