Copper-catalyzed aminobromination/elimination process: an efficient access to α,β-unsaturated vicinal haloamino ketones and esters
Organic & Biomolecular Chemistry2010Vol. 8(19), pp. 4236–4236
Citations Over TimeTop 15% of 2010 papers
Abstract
A novel copper-catalyzed aminobromination-elimination process has been developed, which provides an easy access to alpha,beta-unsaturated vicinal haloamindes derivatives from readily available alpha,beta-unsaturated ketones and esters in good to excellent yields. The isolated intermediate discloses that the current system proceeds through the aminobromination process.
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