Abstract
Herein, we report the catalytic allylic amination of α-methylalkenes with V2O3Dipic2(HMPA)2 and chloramine T as the quantitative source of N. The reaction works with high yields and stereoselectivities for α-methylalkenes. A proposed tosylnitrene-free catalytic cycle involving the formation of vanadoxaziridine complex 1 as the active catalyst and aminovanadation across the substrate as the rate-determining step has been proposed. Initial kinetic and competition experiments provide evidence for the proposed mechanism.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 4001-4008 |
| Number of pages | 8 |
| Journal | Journal of Organic Chemistry |
| Volume | 89 |
| Issue number | 6 |
| DOIs | |
| State | Published - Mar 15 2024 |
All Science Journal Classification (ASJC) codes
- Organic Chemistry