General chiral route to irregular monoterpenes via a common intermediate: syntheses of (S)-lavandulol, cis(1S,3R)-chrysanthemol, (1R,2S)-rothrockene, and (R)-santolinatriene
- 1 April 1985
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 50 (7) , 931-936
- https://doi.org/10.1021/jo00207a004
Abstract
No abstract availableThis publication has 4 references indexed in Scilit:
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- Synthetic study of (+)-nootkatone from (-)-.beta.-pineneThe Journal of Organic Chemistry, 1980
- Non-head-to-tail monoterpenes. Synthesis of (S)-lyratol and (S)-lyratyl acetate from (1R,3R)-chrysanthemic acidThe Journal of Organic Chemistry, 1979
- Model studies of the biosynthesis of non-head-to-tail terpenes. Rearrangements of the chrysanthemyl systemJournal of the American Chemical Society, 1977