130870-89-2Relevant academic research and scientific papers
Palladium-catalysed regioselective sequential C-5 and C-2 direct arylations of 3-acetylpyrroles with aryl bromides
Xu, Yijing,Zhao, Liqin,Li, Yiqun,Doucet, Henri
, p. 1423 - 1432 (2013)
The PdCl(C3H5)(dppb)/KOAc system was found to be effective for the direct regioselective C-5 arylation of 3-acetylpyrroles with ortho-substituted aryl bromides. This procedure has been found to be tolerant to a variety of functional groups at C-2 of the aryl bromide such as methyl, formyl, nitrile, nitro, hydroxymethyl, chloro, fluoro or trifluoromethyl. The sequential direct C-5 arylation followed by C-2 arylation of such 3-substituted pyrroles allows the synthesis of 2,5-diaryl-3-acetylpyrroles in high yields. Copyright
Oxidative Halogenation of Substituted Pyrroles with Cu(II). Part I. Bromination of some 3-Acetylpyrroles
Petruso, S.,Caronna, S.,Sprio, V.
, p. 1209 - 1211 (2007/10/02)
3-Acetylpyrroles are brominated with copper(II) bromide.The reaction afforded almost quantitatively only nuclear monobromination.Evidence for the structures of final compounds was by mass spectrometry, 1H-nuclear magnetic resonance, ir, and elemental analysis.
