Abstract
Distinct reaction modes of π-allylruthenium complexes, derived from allylic acetals, in the urazole-directed C–H/N–H annulation are described. By controlling the reaction conditions, electrophilic addition of π-allylruthenium complexes at the α- and γ-positions was selectively achieved, resulting in the formation of dihydrocinnolines and benzodiazepines, respectively. A series of control experiments for plausible reaction mechanism were performed.
| Original language | English |
|---|---|
| Pages (from-to) | 11806-11811 |
| Number of pages | 6 |
| Journal | Organic Letters |
| Volume | 27 |
| Issue number | 42 |
| DOIs | |
| State | Published - 24 Oct 2025 |
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