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: Labriola, Rafael A., Deulofeu, Venancio, Berinzaghi, Blanca G.
Publicado: 1951
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
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spelling paper:paper_00223263_v16_n1_p90_Labriola2023-06-08T14:49:20Z Studies in argentine plants. XI. The partial structure of erysovine, erysodine, and erysopine Labriola, Rafael A. Deulofeu, Venancio Berinzaghi, Blanca G. 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. Fil:Labriola, R.A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Deulofeu, V. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Berinzaghi, B. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. 1951 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
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
description 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.
author Labriola, Rafael A.
Deulofeu, Venancio
Berinzaghi, Blanca G.
spellingShingle Labriola, Rafael A.
Deulofeu, Venancio
Berinzaghi, Blanca G.
Studies in argentine plants. XI. The partial structure of erysovine, erysodine, and erysopine
author_facet Labriola, Rafael A.
Deulofeu, Venancio
Berinzaghi, Blanca G.
author_sort Labriola, Rafael A.
title Studies in argentine plants. XI. The partial structure of erysovine, erysodine, and erysopine
title_short Studies in argentine plants. XI. The partial structure of erysovine, erysodine, and erysopine
title_full Studies in argentine plants. XI. The partial structure of erysovine, erysodine, and erysopine
title_fullStr Studies in argentine plants. XI. The partial structure of erysovine, erysodine, and erysopine
title_full_unstemmed Studies in argentine plants. XI. The partial structure of erysovine, erysodine, and erysopine
title_sort studies in argentine plants. xi. the partial structure of erysovine, erysodine, and erysopine
publishDate 1951
url 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
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