Applications of the 3-methyl-.gamma.-butyrolactone strategy to the synthesis of polypropionates: the Prelog-Djerassi lactonic ester, ent-invictolide, and the C19-C27 fragment of rifamycin S

This publication has 10 references indexed in Scilit:

• 3-Methyl-.gamma.-butyrolactones as templates for the synthesis of polypropionates: the basic strategy
  Journal of the American Chemical Society, 1988
• Stereocontrolled synthesis of highly oxygenated acyclic systems via the enolate Claisen rearrangement of O-protected allylic glycolates
  The Journal of Organic Chemistry, 1987
• Expeditious synthesis of the polypropionate sector of rifamycin S by reiterative Diene-Aldehyde cyclocondensation reactions
  Journal of the American Chemical Society, 1987
• Di- and trisubstituted .gamma.-lactones. Conformational study by molecular mechanics calculations and coupling constant analysis
  The Journal of Organic Chemistry, 1986
• Stereocontrolled Synthesis of an Epimer of the C(19)‐to‐C(27) Segment of Rifamycin S
  Helvetica Chimica Acta, 1986
• Synthesis of both the enantiomers invictolide, a pheromone component of the red imported fire ant
  Tetrahedron, 1986
• Carbon-carbon bond-forming reactions using cerium metal or organocerium(III) reagents
  The Journal of Organic Chemistry, 1984
• Assembly of the c19-c29 aliphatic segment of rifamycin s from d-glucose by the chiron approach
  Tetrahedron, 1984
• The synthesis of chiral subunits for macrolide synthesis: the Prelog-Djerassi lactone and derivatives
  The Journal of Organic Chemistry, 1981
• 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