An Efficient Route to 1-Vinylpyrrole-2-carbaldehydes
Al'bina I. Mikhaleva, Andrey V. Ivanov, Elena V. Skital'tseva, Igor' A. Ushakov, Alexander M. Vasil'tsov, Boris A. Trofimov*
*A. E. Favorsky Irkutsk Institute of Chemistry, Siberian
Branch of the Russian Academy of Sciences, 1 Favorsky Street, 664033 Irkutsk,
Russian Federation, Email: boris_trofimov
irioch.irk.ru
A. I. Mikhaleva, A. V. Ivanoc, E. V. Skital'tseva, I. A. Ushakov, A. M. Vasil'tsov, B. A. Trofimov, Synthesis, 2009, 587-590.
DOI: 10.1055/s-0028-1083312
Abstract
1-Vinylpyrroles are formylated by the N,N-dimethylformamide/oxalyl chloride reagent system to give the corresponding 1-vinylpyrrole-2-carbaldehydes in good yields in short reaction times.
see article for more examples
While ads financed 62% of the published abstracts in 2024, donations allowed us to publish additional 12%. 26% of the abstracts have been published voluntarly. If you kindly donate, we can publish more freely accessible information and help the chemical community even more:
If you don't like pawalls or a flood of more and more advertising, then you can send a clear signal here!
Key Words
aldehydes, pyrroles, formylation, oxalyl chloride, Vilsmeier-Haack reaction
ID: J66-Y2009-0470
