223384-52-9Relevant academic research and scientific papers
The ester dienolate [2,3]-Wittig rearrangement. Diastereoselective synthesis of 2,3-dialkenyl-substituted 2-hydroxy-γ-lactones
Hiersemann, Martin
, p. 2625 - 2638 (2007/10/03)
The ester dienolate [2,3]-Wittig rearrangement proceeds with high yield and anti/syn diastereoselection to afford 3-alkoxycarbonyl-3-hydroxy- substituted 1,5-hexadienes. No donor solvent or metal salt additive was necessary to trigger the rearrangement. T
