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 synthons

This publication has 5 references indexed in Scilit:

• Synthetic studies on (2R,4'R,8'R)-.alpha.-tocopherol. An approach utilizing side chain synthons of microbiological origin
  The 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 synthon
  The 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 rearrangements
  The Journal of Organic Chemistry, 1976
• Syntheses of (2R, 4′R, 8′R)‐α‐Tocopherol and (2R, 3′E, 7′E)‐α‐Tocotrienol
  Helvetica Chimica Acta, 1976
• Über die Chemie des Vitamins E. 3. Mitteilung. Die Totalsynthese von (2R, 4′R, 8′R)‐ und (2S, 4′R, 8′R)‐α‐Tocopherol
  Helvetica Chimica Acta, 1963