141739-95-9Relevant academic research and scientific papers
Erythroselective aldol condensation of amine free 2-t-butyl-5-methyl-2-phenyl-1,3-dioxolan-4-one lithium enolate synthesis of the ethyl acetolactate enantiomers
Greiner,Ortholand
, p. 1897 - 1900 (2007/10/02)
Generated by halogen metal exchange, the sterically hindered 2-t-butyl-5-methyl-2-phenyl-1,3-dioxolan-4-one lithium enolate reacts in an erythroselective way with acetaldehyde. Separation of the resulting diastereomers, followed by alcoholysis lead to the
