Studies in terpenoid biosynthesis. Part IV. Biosynthesis of the kaurenolides and gibberellic acid
- 1 January 1969
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society C: Organic
- No. 6,p. 981-985
- https://doi.org/10.1039/j39690000981
Abstract
Geranylgeraniol and (–)-labda-8,13-dien-15-ol pyrophosphate have been shown to act as precursors of (–)-kaurene, the kaurenolides, and gibberellic acid. The labelling pattern from 4-(R)-[4-3H]- and 2-[3H2]-mevalonic acid in these tetracyclic diterpenes has been determined and this evidence is used to exclude (–)-primara-7,8- and -8,9-dienes from the biosynthesis. (–)Pimara-8(14)-diene has been shown to be specifically incorporated into the kaurenolides and gibberellic acid. The stereochemistry of hydroxylation of ring A of the gibberellins has been shown to proceed with retention of configuration. The loss of the angular C-20 atom in the formation of the C-19 gibberellins does not involve the decarboxylation of a 4-, 4b-, or 10a-unsaturated acid.Keywords
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