Reactions of 1-aryl-2,5-dimethylpyrroles with ketones
✍ Scribed by O. Pushechnikov; S. P. Ivonin; A. A. Chaikovskaya; T. N. Kudrya; V. V. Pirozhenko; A. A. Tolmachev
- Publisher
- Springer US
- Year
- 1999
- Tongue
- English
- Weight
- 238 KB
- Volume
- 35
- Category
- Article
- ISSN
- 0009-3122
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## Abstract The reaction of 1,4‐naphthoquinone (**1**) with 2,5‐dimethylpyrroles (**7a‐7d**) gives only 3‐(1,4‐naphtho‐quinonyl)‐2,5‐dimethylpyrroles. Extending the reaction to other quinones: 5‐hydroxy‐1,4‐naphthoquinone (**2**), 1,2‐naphthoquinone (**3**), quinoline‐5,8‐dione (**4**) and quinoxal
The chemical reaction of 2,5-dimethylpyrrole (CsHgN) with Oz('A,) ## (W) CsHgN + oz('Ag) -CsHgNOz was studied in the gas phase in an isothermal flow reactor at room temperature and low pressures. The CsHgN concentration profiles were studied under pseudo-first order conditions ([CeHgN], < [Oz('A,