95412-07-0Relevant academic research and scientific papers
PYRROLES FROM KETOXIMES AND ACETYLENE. XXXVII. USE OF VINYL CHLORIDE INSTEAD OF ACETYLENE FOR SYNTHESIS OF ARYLPYRROLES FROM ETHYL ARYL KETONE OXIMES
Aliev, I. A.,Zeinalova, S. N.,Gasanov, B. R.,Mikhaleva, A. I.,Korostova, S. E.
, p. 2198 - 2200 (2007/10/02)
The reaction of ethyl aryl ketone oximes with vinyl chloride in the potassium hydroxide-DMSO system at 130 deg C and atmospheric pressure leads to the formation of 2-aryl-3-methylpyrroles and their N-vinyl derivatives (Ar = p-RC6H4, where R = H, Me, Et, i
PYRROLES FROM KETOXIMES AND ACETYLENE. XXVI. THE SYNTHESIS OF NEW 2-ARYLPYRROLES
Korostova, S. E.,Sobenina, L. N.,Nesterenko, R. N.,Aliev, I. A.,Mikhaleva, A. I.
, p. 1790 - 1793 (2007/10/02)
New representatives of the 2-arylpyrrole series were obtained with yields of 36-90percent from the oximes of alkyl aryl ketones by the Trofimov reaction.When vinyl chloride was used instead of acetylene under the same conditions (potassium hydroxide-DMSO, 80-100 deg C), the pyrroles were obtained with yields of 2-7percent.
