| Autor: |
Dozorova, E. N., Kadushkin, A. V., Bogdanova, G. A., Solov'eva, N. P., Granik, V. G. |
| Zdroj: |
Chemistry of Heterocyclic Compounds; June 1991, Vol. 27 Issue: 6 p590-594, 5p |
| Abstrakt: |
1-Cyanomethyl-2-cyaniminopyrrolidine was synthesized by the reaction of 1-cyanomethyl-2-pyrrolidone diethylacetal with cyanamide. The product undergoes Thorpe—Ziegler cyclization under the influence of sodium ethoxide to give 2-amino-3-cyano-5,6-dihydro-7H-pyrrolo[1,2-a]imidazole, from which 4-amino derivatives of pyrrolo[2,1-f]purine were synthesized. |
| Databáze: |
Supplemental Index |
| Externí odkaz: |
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