132907-21-2Relevant academic research and scientific papers
PYRROLES FROM KETOXIMES AND ACETYLENE. 46. PYRROLES WITH STERICALLY HINDERED SUBSTITUENTS
Aliev, I. A.,Korostova, S. E.,Mikhaleva, A. I.,Shevchenko, S. G.,Zeinalova, S. N.,et al.
, p. 1055 - 1058 (2007/10/02)
The corresponding pyrroles and their N-vinyl derivatives were obtained by the catalyzed (by an MOH-DMSO superbase) reaction of acetylene and its crypto forms (vinyl chloride, 1,2-dichloroethane) with alkyl-2,4-, alkyl-2,5-, and alkyl-3,4-dimethylphenylketoximes.Reaction intermediates - O-vinylketoximes - were detected.
Reactivity of 3,6-dimethoxy-3,6-dimethylcyclohexa-1,4-diene (Part 2). Regioselective arylation of electron-rich aromatic compounds
Alonso,Yus
, p. 313 - 316 (2007/10/02)
The reaction of 3,6-dimethoxy-3,6-dimethylcyclohexa-1,4-diene (1) with electron-rich heterocycles (furan, thiophene, pyrrole, 2-methylfuran, indole) and 1,3,5-trimethoxybenzene in the presence of catalytic amounts of zinc dichloride or concentrated sulfur
Arylation of N-Acyl-pyrroles and -indoles with Arenes and Palladium Acetate
Itahara, Toshio
, p. 254 - 255 (2007/10/02)
Treatment of 1-benzoylpyrroles with palladium acetate in acetic acid containing benzene gave mixtures of 1-benzoyl-2-phenylpyrroles; similar treatment of 1-acetylindoles gave the corresponding 1-acetyl-2-phenylindoles.
