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Ligand-Enabled Triple CH Activation Reactions: One-Pot Synthesis of Diverse 4-Aryl-2-quinolinones from Propionamides
Ist Teil von
Angewandte Chemie (International ed.), 2014-06, Vol.53 (26), p.6692-6695
Ort / Verlag
Weinheim: WILEY-VCH Verlag
Erscheinungsjahr
2014
Link zum Volltext
Quelle
Alma/SFX Local Collection
Beschreibungen/Notizen
Diverse 4‐aryl‐2‐quinolinones are prepared from propionamides in one pot by ligand‐promoted triple sequential CH activation reactions and a stereospecific Heck reaction. In these cascade reactions, three new CC bonds and one CN bond are formed to rapidly build molecular complexity from propionic acid.
Building complexity: Diverse 4‐aryl‐2‐quinolinones such as 1 are prepared from propionamides in one pot by pyridine ligand‐promoted triple sequential CH activation reactions and a stereospecific Heck reaction. In these cascade reactions, three new CC bonds and one CN bond are formed to rapidly build molecular complexity from propionic acid.