360579-41-5Relevant academic research and scientific papers
Diastereoselective synthesis of (2R,4R)-2-aryl-4-hydroxypyrrolidine: Preparation of the side chain of novel carbapenem
Hashihayata,Sakoh,Goto,Hirose,Sakuraba,Imamura,Sugimoto,Yamada,Morishima
, p. 1500 - 1502 (2007/10/03)
Improved synthesis of the trans-3,5-disubstituted pyrrolidin-3-ylthio side-chain of the novel carbapenem 1 was achieved via stereoselective reduction of the 1-aryl-1-butanone derivative 5 and successive intramolecular cyclization of the resulting chiral alcohol 6. The 1-aryl-1-butanone derivative 5 was obtained by a coupling reaction of protected 4-hydroxy-2-pyrrolidone with aryl-Grignard reagent.
