Stereocontrolled synthesis of highly oxygenated acyclic systems via the enolate Claisen rearrangement of O-protected allylic glycolates

This publication has 13 references indexed in Scilit:

• Asymmetric reductions of .alpha.,.beta.-acetylenic ketones and acetophenone using lithium aluminum hydride complexed with optically active 1,3-amino alcohols
  The Journal of Organic Chemistry, 1980
• Enolate Claisen rearrangement of esters from furanoid and pyranoid glycals
  The Journal of Organic Chemistry, 1980
• Synthesis of (2R,4'R,8'R)-.alpha.-tocopheryl acetate (vitamin E acetate) using [3,3] sigmatropic rearrangement
  The Journal of Organic Chemistry, 1978
• Total synthesis of (.+-.)-sarracenin
  The 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 synthons
  The Journal of Organic Chemistry, 1977
• Absolute configuration of (−)-4-methylheptan-3-ol, a pheromone of the smaller european elm bark beetle, as determined by the synthesis of its (3R,4R)-(+)- and (3S,4R)-(+)-isomers
  Tetrahedron, 1977
• 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
• Sex Pheromone Specificity in the Pine Sawflies: Interchange of Acid Moieties in an Ester
  Science, 1976