| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5223306 | Tetrahedron | 2010 | 9 Pages |
Abstract
Studies directed at the amine exchange reaction of vinamidinium salts followed by sodium borohydride reduction to secondary and tertiary allylic amines are described. The tertiary allylic amines were alkylated and subjected to base mediated rearrangement to yield a variety of highly functionalized tertiary homoallylic amines.
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