| | 1 | Author
| J. B. Stothers, A. Stoessl, E.W B Ward | Requires cookie* | | | Title
|  | | | | Abstract
| The mechanism of the biological hydroxylation of the isopropenyl side-chain of the sesquiterpene capsidiol, to give 13-hydroxycapsidiol, has been investigated with 13C-N M R techniques, using capsidiol biogenetically enriched with 13C from [l^-^CU] acetate. The results indicate that neither an allylic rearrangement nor the formation of an epoxide intervene in the process. | | | |
Reference
| Z. Naturforsch. 33c, 149—150 (1978); eingegangen am 30. Dezember 1977 | | | |
Published
| 1978 | | | |
Keywords
| Biosynthesis, Capsidiol, 13C-NMR, Phytoalexins, Sesquiterpenes | | | |
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| default:Reihe_C/33/ZNC-1978-33c-0149_n.pdf | | | | Identifier
| ZNC-1978-33c-0149_n | | | | Volume
| 33 | |
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