1283733-07-2Relevant academic research and scientific papers
A general, asymmetric, and noniterative synthesis of trideoxypropionates. Straightforward syntheses of the pheromones (+)-vittatalactone and (+)-norvittatalactone
Weise, Christian F.,Pischl, Matthias C.,Pfaltz, Andreas,Schneider, Christoph
, p. 1477 - 1488 (2012/04/04)
A novel, highly stereocontrolled, and very flexible synthetic access to biologically relevant trideoxypropionate building blocks in optically pure form has been developed. On the basis of a three-step sequence comprising a thermal oxy-Cope rearrangement,
A non-iterative, flexible, and highly stereoselective synthesis of polydeoxypropionates-synthesis of (+)-vittatalactone
Weise, Christian F.,Pischl, Matthias,Pfaltz, Andreas,Schneider, Christoph
, p. 3248 - 3250 (2011/05/05)
A short sequence comprising an oxy-Cope rearrangement, iridium-catalyzed hydrogenation, and enolate methylation provides trideoxypropionates with excellent diastereocontrol. A straightforward synthesis of the cucumber beetle pheromone (+)-vittatalactone i
