1. Crystal structure of HIV-1 protease in complex with VX-478, a potent and orally bioavailable inhibitor of the enzyme
2. Novel spirocyclic pyrrolidones as P2/P1 mimetics in potent inhibitors of HIV-1 protease
3. Tung, R., Hale, M., Baker, C., Furfine, E.; Kaldor, I.; Kazmierski, W., Spaltenstein, A. PTC Int. Appl. WO 9933815.
4. Hale, M.; Tung, R.; Baker, C.; Spaltenstein, A.; Furfine. E.; Kaldor, I., Kazmierski, W. PCT Int. Appl. WO 9933795
5. Hale, M.; Tung, R.; Baker, C.; Spaltenstein, A.; Furfine, E.; Kaldor, I., Kazmierski, W. PCT Int. Appl. WO 9933793