Synthesis of (2R,4'R,8'R)-.alpha.-tocopheryl acetate (vitamin E acetate) using [3,3] sigmatropic rearrangement
- 1 September 1978
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 43 (18) , 3435-3440
- https://doi.org/10.1021/jo00412a001
Abstract
No abstract availableThis publication has 4 references indexed in Scilit:
- Synthetic studies on (2R,4'R,8'R)-.alpha.-tocopherol. An approach utilizing side chain synthons of microbiological originThe Journal of Organic Chemistry, 1976
- Synthetic studies on (2R,4'R,8'R)-.alpha.-tocopherol. Facile syntheses of optically active, saturated, acyclic isoprenoids via stereospecific [3,3] sigmatropic rearrangementsThe Journal of Organic Chemistry, 1976
- PALLADIUM CATALYST FOR PARTIAL REDUCTION OF ACETYLENESOrganic Syntheses, 1966
- Über die Chemie des Vitamins E. 3. Mitteilung. Die Totalsynthese von (2R, 4′R, 8′R)‐ und (2S, 4′R, 8′R)‐α‐TocopherolHelvetica Chimica Acta, 1963