The absolute configuration of santolina alcohol from ormenis multicaulis
- 31 December 1972
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 13 (1) , 71-74
- https://doi.org/10.1016/s0040-4039(01)84242-8
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
- Stereospecific homoallylic ring expansions and contractionsJournal of the American Chemical Society, 1970
- Stereospecific cationic rearrangements of syn- and antibicyclo[6.1.0]nonane derivativesJournal of the American Chemical Society, 1970
- The structure and stereochemistry of lyratol a new C10 alcohol from Cyathocline lyrataTetrahedron, 1969
- Requirements for the artemisyl, santolinyl and lavandulyl fissions of chrysanthemic acid relatives under carbonium ion type initiationTetrahedron Letters, 1967
- Terpenoids. IX. Biogenesis of some monoterpenoids not derived from a geranyl precursorTetrahedron Letters, 1965
- 948. Synthesis, absolute configuration, and ring-fission of cis- and trans-homocaronic acid: their configurative relation to natural terpenesJournal of the Chemical Society, 1963