Abstract
Abstractπ‐Allyltitanium complexes, generated in situ from 1,3‐dienes and [Cp2TiH], react with benzotriazole derivatives to give homoallylic amines in good yields. Under similar conditions, triple cascade reactions (allyltitanation followed by cationic 2‐aza‐Cope rearrangement followed by a second allyltitanation) occur from bis(benzotriazolyl) compounds affording a straightforward route to homoallyl‐(E)‐homocrotylamines. A theoretical study provides further insight into the factors that govern the selectivity of this sequence of reactions.
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