Biosynthesis of skimmianine in Fagara coco

Fagara coco plants were inoculated in separate experiments with sodium acetate 1-14C, sodium formate-14C, mevalonic acid-4-14C, mevalonic acid-5-14C, 3,3-dimethylallyl alcohol-1-14C, and 3,3-dimethylacrylic acid-1-14C. The furanoquinoline alkaloid skimmianine was isolated from each plant and degrade...

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Autores principales: Colonna, A.O., Gros, E.G.
Formato: JOUR
Acceso en línea:http://hdl.handle.net/20.500.12110/paper_00319422_v10_n7_p1515_Colonna
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spelling todo:paper_00319422_v10_n7_p1515_Colonna2023-10-03T14:43:48Z Biosynthesis of skimmianine in Fagara coco Colonna, A.O. Gros, E.G. Fagara coco plants were inoculated in separate experiments with sodium acetate 1-14C, sodium formate-14C, mevalonic acid-4-14C, mevalonic acid-5-14C, 3,3-dimethylallyl alcohol-1-14C, and 3,3-dimethylacrylic acid-1-14C. The furanoquinoline alkaloid skimmianine was isolated from each plant and degraded to determine the activity at C-2 and C-3. The result from the acetate experiment confirmed previous findings for labelling only in the quinoline moiety; the same result was encountered with labelled dimethylacrylic acid. Sodium formate labelled mainly the methoxy groups, while the results from both mevalonic acids and dimethylallyl alcohol clearly indicated that C-2 and C-3 of the furan ring are derived from C-4 and C-5 of mevalonic acid respectively. © 1971. Fil:Colonna, A.O. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Gros, E.G. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_00319422_v10_n7_p1515_Colonna
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
description Fagara coco plants were inoculated in separate experiments with sodium acetate 1-14C, sodium formate-14C, mevalonic acid-4-14C, mevalonic acid-5-14C, 3,3-dimethylallyl alcohol-1-14C, and 3,3-dimethylacrylic acid-1-14C. The furanoquinoline alkaloid skimmianine was isolated from each plant and degraded to determine the activity at C-2 and C-3. The result from the acetate experiment confirmed previous findings for labelling only in the quinoline moiety; the same result was encountered with labelled dimethylacrylic acid. Sodium formate labelled mainly the methoxy groups, while the results from both mevalonic acids and dimethylallyl alcohol clearly indicated that C-2 and C-3 of the furan ring are derived from C-4 and C-5 of mevalonic acid respectively. © 1971.
format JOUR
author Colonna, A.O.
Gros, E.G.
spellingShingle Colonna, A.O.
Gros, E.G.
Biosynthesis of skimmianine in Fagara coco
author_facet Colonna, A.O.
Gros, E.G.
author_sort Colonna, A.O.
title Biosynthesis of skimmianine in Fagara coco
title_short Biosynthesis of skimmianine in Fagara coco
title_full Biosynthesis of skimmianine in Fagara coco
title_fullStr Biosynthesis of skimmianine in Fagara coco
title_full_unstemmed Biosynthesis of skimmianine in Fagara coco
title_sort biosynthesis of skimmianine in fagara coco
url http://hdl.handle.net/20.500.12110/paper_00319422_v10_n7_p1515_Colonna
work_keys_str_mv AT colonnaao biosynthesisofskimmianineinfagaracoco
AT groseg biosynthesisofskimmianineinfagaracoco
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