227095-33-2Relevant academic research and scientific papers
Diastereoselective synthesis of a novel lactam peptidomimetic exploiting vinylogous Mannich addition of 2-silyloxyfuran reagents
Battistini, Lucia,Rassu, Gloria,Pinna, Luigi,Zanardi, Franca,Casiraghi, Giovanni
, p. 765 - 773 (2007/10/03)
The total synthesis of a potential inhibitor of HIV-protease-the chiral nonracemic six-membered hydroxy lactam 6-has been accomplished, that involves, as key reaction, the highly diastereoselective vinylogous Mannich addition of furan-based silyloxy diene 7 to glyceraldeyde imine 8.
