503441-71-2Relevant academic research and scientific papers
Highly diastereoselective Michael reaction of (S)-mandelic acid enolate. Chiral benzoyl carbanion equivalent through an oxidative decarboxylation of α-hydroxyacids
Blay, Gonzalo,Fernández, Isabel,Monje, Belén,Pedro, José R,Ruiz, Rafael
, p. 8463 - 8466 (2002)
The reaction of the lithium enolate of the 1,3-dioxolan-4-one derived from optically active (S)-mandelic acid and pivalaldehyde with α,β-unsaturated carbonyl compounds proceeds readily to give the corresponding Michael adducts in good yields and high dias
