186517-11-3Relevant academic research and scientific papers
Diastereoselectivity of enolate anion protonation. H/D exchange of β-substituted ethyl butanoates in ethanol-d
Mohrig, Jerry R.,Rosenberg, Robert E.,Apostol, John W.,Bastienaansen, Mark,Evans, Jordan W.,Franklin, Sonya J.,Frisbie, C. Daniel,Fu, Sabrina S.,Hamm, Michelle L.,Hirose, Christopher B.,Hunstad, David A.,James, Thomas L.,King, Randall W.,Larson, Christopher J.,Latham, Hallie A.,Owen, David A.,Stein, Karin A.,Warnet, Ronald
, p. 479 - 486 (1997)
The stereochemistry of base-catalyzed H/D exchange on 13 β-substituted ethyl butanoates in ethanol-d has been studied in order to analyze the steric and electronic factors which control the diastereoselectivity of electrophilic attack on enolate anions. E
