10.1021/jo401967a.s003 José A. Gálvez José A. Gálvez María D. Díaz-de-Villegas María D. Díaz-de-Villegas Miriam Alías Miriam Alías Ramón Badorrey Ramón Badorrey Chiral Iminoesters Derived from d‑Glyceraldehyde in [3 + 2] Cycloaddition Reactions. Asymmetric Synthesis of a Key Intermediate in the Synthesis of Neuramidinase Inhibitors American Chemical Society 2013 Key Intermediate cycloaddition synthesis Neuramidinase chiral iminoesters reaction diastereoselectively approach pyrrolidine influenza neuramidinase inhibitors Asymmetric Synthesis Chiral Iminoesters Derived functionalized pyrrolidines acrylate Cycloaddition 2013-11-15 00:00:00 Dataset https://acs.figshare.com/articles/dataset/Chiral_Iminoesters_Derived_from_d_Glyceraldehyde_in_3_2_Cycloaddition_Reactions_Asymmetric_Synthesis_of_a_Key_Intermediate_in_the_Synthesis_of_Neuramidinase_Inhibitors/2352706 Silver-catalyzed <i>endo</i>-selective and copper-catalyzed <i>exo</i>-selective asymmetric [3 + 2] cycloadditions of acrylates to chiral iminoesters derived from d-glyceraldehyde have been investigated. The reaction diastereoselectively provides highly functionalized pyrrolidines. This approach was used to develop the first asymmetric synthesis of a key intermediate in the synthesis of pyrrolidine influenza neuramidinase inhibitors.