Add to ORKGThe stereoselective synthesis of (−)-6-acetoxyhexadecanolide was achieved from the readily available chiral pool compound, l-(+)-tartaric acid. The synthetic sequence includes the elaboration of an α-benzyloxy aldehyde derived from tartaric acid with ring closing metathesis as the key step
Enantiodivergent synthesis of both (-)- and (+)-disparlure, a bioactive pheromone, possessing a cis-...
Department of Chemistry, East Texas State University, Commerce, Texas-75428, U. S. A. Manuscript re...
A short sequence comprising an oxy-Cope rearrangement, iridium-catalyzed hydrogenation, and enolate ...
The stereoselective synthesis of (−)-6-acetoxyhexadecanolide was achieved from the readily available...
An efficient asymmetric synthesis of 5-hexadecanolide from a chiral epoxide is described. Both the e...
Enantioselective synthesis of α-hydroxy aldehydes with an alkene tether was accomplished from L...
Both antipodes of α-methyl-α-methoxyarylacetic acid derivatives were prepared from a commo...
Both antipodes of a-methyl-a-methoxyarylacetic acid derivatives were prepared from a common chiralpo...
An efficient (12 steps, 12% overallyield) and stereoselective total synthesis of (±)-serricornine (1...
The asymmetric total synthesis of naturally occurring insect pheromones, (R)-4-dodecanolide and (S)-...
Enantiodivergent synthesis of both (−)- and (+)-disparlure, a bioactive pheromone, possessing a cis-...
The enantioselective synthesis of α-benzyloxy aldehydes containing a terminal alkene was carrie...
The thesis entitled “Enantioselective synthesis of bio-active bicyclic acetals, cyclic ethers and la...
A convergent synthesis of four stereoisomers of the sex pheromone of the western corn rootworm (8-me...
A concise enantiospecific synthesis of the pine beetle pheromone (+)-hydroxy-exo-brevicomin was achi...
Enantiodivergent synthesis of both (-)- and (+)-disparlure, a bioactive pheromone, possessing a cis-...
Department of Chemistry, East Texas State University, Commerce, Texas-75428, U. S. A. Manuscript re...
A short sequence comprising an oxy-Cope rearrangement, iridium-catalyzed hydrogenation, and enolate ...
The stereoselective synthesis of (−)-6-acetoxyhexadecanolide was achieved from the readily available...
An efficient asymmetric synthesis of 5-hexadecanolide from a chiral epoxide is described. Both the e...
Enantioselective synthesis of α-hydroxy aldehydes with an alkene tether was accomplished from L...
Both antipodes of α-methyl-α-methoxyarylacetic acid derivatives were prepared from a commo...
Both antipodes of a-methyl-a-methoxyarylacetic acid derivatives were prepared from a common chiralpo...
An efficient (12 steps, 12% overallyield) and stereoselective total synthesis of (±)-serricornine (1...
The asymmetric total synthesis of naturally occurring insect pheromones, (R)-4-dodecanolide and (S)-...
Enantiodivergent synthesis of both (−)- and (+)-disparlure, a bioactive pheromone, possessing a cis-...
The enantioselective synthesis of α-benzyloxy aldehydes containing a terminal alkene was carrie...
The thesis entitled “Enantioselective synthesis of bio-active bicyclic acetals, cyclic ethers and la...
A convergent synthesis of four stereoisomers of the sex pheromone of the western corn rootworm (8-me...
A concise enantiospecific synthesis of the pine beetle pheromone (+)-hydroxy-exo-brevicomin was achi...
Enantiodivergent synthesis of both (-)- and (+)-disparlure, a bioactive pheromone, possessing a cis-...
Department of Chemistry, East Texas State University, Commerce, Texas-75428, U. S. A. Manuscript re...
A short sequence comprising an oxy-Cope rearrangement, iridium-catalyzed hydrogenation, and enolate ...