187409-26-3Relevant articles and documents
Enantioselective synthesis of (2S,3S)- and (2R,3R)-pyrrolidine-2,3-dicarboxylic acids: Conformationally constrained (S)- and (R)-aspartic acid analogues
Andre Sasaki,Pauly, Regine,Fontaine, Catherine,Chiaroni, Angele,Riche, Claude,Potier, Pierre
, p. 241 - 244 (1994)
The title compounds were prepared from the key intermediate 2 and its enantiomer at C2, derived from chiral synthons 1-(R) and 1- (S), respectively, by ethoxycarbonylation, desulfonylation and conversion to carboxylic acid.