The chemical and microbiological preparation of 15-oxo-Gibberellin derivatives
The biotransformation of 15-oxo-ent-kaur-16-ene (1) with the fungus Gibberella fujikuroi gave 16a, 17-dihydro-7B-hydroxy-15-oxo-kaurenolide (5), 16a, 17-dihydro-15-oxo-GA12 (7) 16a,17-dihydro-15-oxo-GA25 (8) 16a,17-dihydro-15-oxo-GA24 (9), 7-aldehhyde of 16a,17-dihydro-15-oxo-GA14 (10), ent-3a,7a-15-oxo-kauran-19-oic acid (11), and 16a,17-dihydro-15-oxo-GA7 (12). The hydrogenation of the 16,17-double bond observed in this incubation is directed by the presence of the 15-oxo group, and it does not take place in the normal biosynthetic gibberellin pathway. The Chemical preparation of some of these 15-oxo-gibberellins has also been carried out.
Main Authors: | , , , , |
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Format: | artículo biblioteca |
Language: | English |
Published: |
Elsevier
1995
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Online Access: | http://hdl.handle.net/10261/21718 http://dx.doi.org/10.13039/501100008737 |
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