173091-87-7Relevant academic research and scientific papers
Pyrrolinone-based HIV protease inhibitors. Design, synthesis, and antiviral activity: Evidence for improved transport
Smith III, Amos B.,Hirschmann, Ralph,Pasternak, Alexander,Guzman, Mark C.,Yokoyama, Akihisa,Sprengeler, Paul A.,Darke, Paul L.,Emini, Emilio A.,Schleif, William A.
, p. 11113 - 11123 (2007/10/03)
Pyrrolinone-based peptidomimetics, the first mimics of β-strands, are potent inhibitors of HIV-1 protease. Importantly, the bis(pyrrolinones) described herein proved to be more active in cellular antiviral assays compared with an analogous peptide-derived
Synthesis of β-hydroxy-γ-trimethylsilyl-γ-butyrolactone as key chiral building block for preparation of four-carbon chain units having tertiary stereogenic carbon
Miyazaki, Yasushi,Hotta, Hiroyasu,Sato, Fumie
, p. 4389 - 4392 (2007/10/02)
A new chiral building block β-hydroxy-γ-trimethylsilyl-γ-butyrolactone (1) was prepared from γ-trimethylsilylallyl acetate (2) via two steps in excellent overall yield. The lactone 1 is a useful precursor to four-carbon chain blocks having tertiary stereogenic centers such as 6, 10 and 11.
