| Autor: |
Goralski, Christian T., Hasha, Dennis L., Nicholson, Lawrence W., Singaram, Bakthan |
| Zdroj: |
Tetrahedron Letters; July 1994, Vol. 35 Issue: 29 p5165-5168, 4p |
| Abstrakt: |
The hydroboration of the enamines derived from 2-norbornanone with BMS followed by methanolysis and oxidation with basic hydrogen peroxide afforded moderate yields of the corresponding endo-3-(dialkylamino)-exo-2-norbornanols. Hydroboration with 9-BBN followed by methanolysis gave excellent yields of the corresponding endo-2-(dialkylamino)norbornanes. |
| Databáze: |
Supplemental Index |
| Externí odkaz: |
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