132907-21-2Relevant academic research and scientific papers
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
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.
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.
