Abstract
A novel copper-catalyzed aminobromination-elimination process has been developed, which provides an easy access to α,β-unsaturated vicinal haloamindes derivatives from readily available α,β-unsaturated ketones and esters in good to excellent yields. The isolated intermediate discloses that the current system proceeds through the aminobromination process.
Original language | English |
---|---|
Pages (from-to) | 4236-4239 |
Number of pages | 4 |
Journal | Organic & Biomolecular Chemistry |
Volume | 8 |
Issue number | 19 |
DOIs | |
State | Published - Oct 7 2010 |