Studies in argentine plants. XI. The partial structure of erysovine, erysodine, and erysopine
1. Treatment of the liberated alkaloids of Erythrina: erysovine, erysodine, and erysopine, with diazomethane gave the same methylated base, erysotrine, which was obtained in crystalline condition. 2. Oxidation of erysotrine gave m-hemipinic acid imide. When erysotrine methohydroxide was oxidized m-h...
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| Autores principales: | , , |
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| Publicado: |
1951
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| Acceso en línea: | https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00223263_v16_n1_p90_Labriola http://hdl.handle.net/20.500.12110/paper_00223263_v16_n1_p90_Labriola |
| Aporte de: |
| Sumario: | 1. Treatment of the liberated alkaloids of Erythrina: erysovine, erysodine, and erysopine, with diazomethane gave the same methylated base, erysotrine, which was obtained in crystalline condition. 2. Oxidation of erysotrine gave m-hemipinic acid imide. When erysotrine methohydroxide was oxidized m-hemipinic acid N-methylimide was obtained. 3. The constitutional relationship between the liberated alkaloids and the free alkaloids erythramine and erytbraline is confirmed. © 1951, American Chemical Society. All rights reserved. |
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