| Autor: |
Kul'nevich, V. G., Zelikman, Z. I., Kapustyanskaya, Zh. V., Glukhovtsev, V. G., Tkachenko, S. E., Zhinzhina, I. S. |
| Zdroj: |
Chemistry of Heterocyclic Compounds; August 1977, Vol. 13 Issue: 8 p823-826, 4p |
| Abstrakt: |
The possibility of the reduction of the furan ring to a tetrahydrofuran ring under the conditions of liquid-phase hydrogenation of 2-furyl-1,3-dioxanes on Raney nickel at atmospheric pressure is demonstrated. 2-Furyl or tetrahydro-2-furyl amino derivatives of 1,3-dioxane are formed in the case of 5-nitro-2-furyl-1,3-dioxanes as a function of the structure of the starting acetals. Data from the UV and IR spectra are presented. |
| Databáze: |
Supplemental Index |
| Externí odkaz: |
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