| Autor: |
Zhestkov, V. P., Mironov, A. F., Evstigneeva, R. P. |
| Zdroj: |
Chemistry of Heterocyclic Compounds; June 1976, Vol. 12 Issue: 6 p656-659, 4p |
| Abstrakt: |
A number of cyanopyrroles were synthesized. The nitrile group was created by treatment of pyrrolecarboxylic acids with p-toluenesulfonamide and phosphorus pentachloride. It was found that the pyrrole ring is rapidly N-methylated in the presence of diazomethane when it contains three electron-acceptor substituents. |
| Databáze: |
Supplemental Index |
| Externí odkaz: |
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