Asymmetric reductions of .alpha.,.beta.-acetylenic ketones and acetophenone using lithium aluminum hydride complexed with optically active 1,3-amino alcohols
- 1 February 1980
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 45 (4) , 582-588
- https://doi.org/10.1021/jo01292a006
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
- Synthesis of (2R,4'R,8'R)-.alpha.-tocopheryl acetate (vitamin E acetate) using [3,3] sigmatropic rearrangementThe Journal of Organic Chemistry, 1978
- Transfer of chirality in the [2,3] sigmatropic rearrangement of allylic alcohols to .beta.,.gamma.-unsaturated amides. Preparation of optically active nine- and fourteen-carbon saturated isoprenoid synthonsThe Journal of Organic Chemistry, 1977
- 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. An alternative synthesis of (2R,6R)-(+)-2,6,10-trimethylundecan-1-ol, a key side chain synthonThe 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
- Syntheses of (2R, 4′R, 8′R)‐α‐Tocopherol and (2R, 3′E, 7′E)‐α‐TocotrienolHelvetica Chimica Acta, 1976