## Abstract For Abstract see ChemInform Abstract in Full Text.
The absolute stereochemistry of hardwickiic acid and its congeners
โ Scribed by R. Misra; R.C. Pandey; Sukh Dev
- Publisher
- Elsevier Science
- Year
- 1968
- Tongue
- French
- Weight
- 224 KB
- Volume
- 9
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
โฆ Synopsis
IN an earlier communicationl, we reported on the structure elucidation of hardwickiic acid (I) and some other related diterpenoids, all constituents of the oleo-resin of Hardwickia pinnata. However, biogenetic considerations were invoked for the placement of the angular methyla as shown in I. We now provide experimental support for the location elucidate the absolute stereochemistry at the provides conclusive evidence for the absolute acid. describe degradation work, designed to of these quaternary methyls, as also to various asymmetric centre8. This work stereostructure II for (-)-hardwickiic
๐ SIMILAR VOLUMES
Three novel cyclopropanoid guaianolides axivalin, ivaxillarin, and anhydroivaxillarin have been isolated from Iva axillaris Pursh. ssp. robustior, and were assigned gross structures I, II, and III, respectively.' To confirm the
We wish to report that the metabolic transformation of (?Z)-epoxyfarnesol (I) by Helminthosporium sativum yielded (-)-lO,ll-dihydroxyfarnesol (II), (-)-lO,ll-dihydroxyfarnesic acid (III) and (-)-9,10-dihydroxygeranylacetone (IV), and that their absolute stereochemistry, as well as
The synthesis of both enantiomers of phosphonothrixin is described. On the basis of optical rotation and biological activity, the natural product was determined to have S configuration.
## Abstract For Abstract see ChemInform Abstract in Full Text.