746639-69-0Relevant academic research and scientific papers
Highly stereoselective oxy-Michael additions to β,γ-unsaturated α-Keto Esters: Rapid enantioselective synthesis of 3-hydroxybutenolides
Xiong, Xin,Ovens, Caroline,Pilling, Adam W.,Ward, John W.,Dixon, Darren J.
, p. 565 - 567 (2008)
The highly diastereoselective oxy-Michael addition of the "naked" anion of (6S)-methyl δ-lactol to γ-substituted β,γ- unsaturated α-keto esters leading to the direct formation of THP*-protected γ-hydroxy α-keto ester derivatives is described. Subsequent a
