Synthesis of PotentC₂-Symmetric, Diol-Based HIV-1 Protease Inhibitors. Investigation of Thioalkyl and Thioaryl P1/P1‘ Substituents

Synthesis of PotentC₂-Symmetric, Diol-Based HIV-1 Protease Inhibitors. Investigation of Thioalkyl and Thioaryl P1/P1‘ Substituents Novel pseudosymmetric inhibitors of HIV-1 protease P1′ oxadiazole protease inhibitors with excellent activity against native and protease inhibitor-resistant HIV-1 Flexible Cyclic Ethers/Polyethers as Novel P2-Ligands for HIV-1 Protease Inhibitors: Design, Synthesis, Biological Evaluation, and Protein−Ligand X-ray Studies Functionalized aliphatic P2/P2′ analogs of HIV-1 protease inhibitor DMP323 Design and synthesis of potent HIV-1 protease inhibitors incorporating hydroxyprolinamides as novel P2 ligands Synthesis and antiviral activity of a series of HIV-1 protease inhibitors with functionality tethered to the P1 or P1' phenyl design Design and Synthesis of New PotentC₂-Symmetric HIV-1 Protease Inhibitors. Use of<scp>l</scp>-Mannaric Acid as a Peptidomimetic Scaffold Potent inhibitors of the HIV-1 protease incorporating cyclic urea P1–P2 scaffold Novel inhibitors of HIV protease