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Asymmetric Total Synthesis of the Gastroprotective Microbial Agent AI-77-B.
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SYNTHESIS AND OPTICAL RESOLUTION OF HIGH AFFINITY P-LIGANDS FOR HIV-1 PROTEASE INHIBITORS.
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Ultra-potent P1 modified arylsulfonamide HIV protease inhibitors: the discovery of GW0385.
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Stereoselective and efficient synthesis of (3R,3aS,6aR)-hexahydrofuro[2,3-b]furan-3-ol.
Org Lett. 2005 Dec 22;7(26):5917-20. doi: 10.1021/ol052554i.
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Discovery and selection of TMC114, a next generation HIV-1 protease inhibitor.
J Med Chem. 2005 Mar 24;48(6):1813-22. doi: 10.1021/jm049560p.

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