654061-24-2Relevant academic research and scientific papers
Preparation of (2,2-Dimethylhexahydrofuro[2,3-c]pyrrol-6-yl)methanol: A Conformationally Restricted Congener of Nonproteinogenic 3-Hydroxy-4- methylproline
Jao, Edwin,Bogen, Stephane,Saksena, Anil K.,Girijavallabhan, Viyyoor
, p. 2643 - 2646 (2007/10/03)
Lactam 6 derived from (S)-pyroglutaminol was converted to a conformationally restricted congener of nonproteinogenic 3-hydroxy-4- methylproline. Preparation of precursor Sb was achieved via a diastereoselective epoxidation followed by a regioselective opening of the oxirane ring. Iodine-mediated cyclization was used to assemble the ether moiety of 2.
