Synthesis of Norbisabolide
- 1 March 1983
- journal article
- research article
- Published by Taylor & Francis in Synthetic Communications
- Vol. 13 (4) , 341-345
- https://doi.org/10.1080/00397918308066986
Abstract
Norbisabolide has been synthesized from limonene 8,9-oxide via malonate alkylation. In situ generation of the terpene synthon from 4-methyl-3-cyclo-hexen-1-yl methyl ketone is demonstrated. Homolimonenol can also serve as precursor of the terpene.Keywords
This publication has 5 references indexed in Scilit:
- A synthesis of γ-lactones by reaction of lithium β-lithiopropionate with aldehydes and ketonesTetrahedron Letters, 1978
- A Synthesis of NorbisabolideSynthetic Communications, 1977
- Oxidation by metal salts. X. One-step synthesis of .gamma.-lactones from olefinsJournal of the American Chemical Society, 1974
- Dimethyloxosulfonium Methylide ((CH3)2SOCH2) and Dimethylsulfonium Methylide ((CH3)2SCH2). Formation and Application to Organic SynthesisJournal of the American Chemical Society, 1965
- Thermal Condensation of Cyclic Olefins with Formaldehyde1,2Journal of the American Chemical Society, 1957