A Facile and Practical Synthesis of N-Acetyl Enamides
The Journal of Organic Chemistry2009Vol. 74(24), pp. 9528–9530
Citations Over TimeTop 15% of 2009 papers
Abstract
A facile and practical method for the synthesis of N-acetyl alpha-arylenamides has been developed from corresponding ketoximes as the starting materials with ferrous acetate as the reducing reagent. This methodology offers mild reaction conditions, simple purification procedures, and high yields for a variety of N-acetyl enamides.
Related Papers
- → N,N‘-Ditosylhydrazine: A Convenient Reagent for Facile Synthesis of Diazoacetates(2007)134 cited
- → Novel one-pot three-step reaction using supported reagents system: synthesis of 2-aminothiazoles(2007)15 cited
- → Silphos as an efficient heterogeneous reagent for the synthesis of 2-azetidinones(2014)5 cited
- → TFFH as an Excellent Reagent for Acylation of Alcohols, Thiols and Dithiocarbamates.(2005)4 cited
- → Parallel synthesis with fluorous reagents and reactants(1999)