620151-84-0Relevant articles and documents
Chemoselective Nucleophilic Attack on N-Acyl Derivatives of (S)-Ethyl 4,4-Dimethyl Pyroglutamate (DMPG)
Mantecon, Susana,Vaquero, Juan J.,Alvarez-Builla, Julio,De La Puente, Maria Luz,Espinosa, Juan F.,Ezquerra, Jesus
, p. 3791 - 3794 (2007/10/03)
(Matrix presented) Heteronucleophiles and C-nucleophiles chemoselectively react with N-acyl (S)-ethyl 4,4-dimethyl pyroglutamate (DMPG) affording esters, amides, and ketones in high yield. The intramolecular process allows the stereoselective formation of β-hydroxy acids likely by formation and ring opening of the corresponding β-lactones.