The synthesis of novel HIV-protease inhibitors

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Abstract

The syntheses, enzyme inhibition and antiviral activity of potent HIV-protease inhibitors containing novel β-hydroxy ether and thioethers based on the transition state mimetic concept are discussed.

The syntheses and enzyme and antiviral activities of potent HIV-protease inhibitors containing novel β-hydroxy ether and thioethers (e. g. 2) based on the transition state mimetic concept are discussed.

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Cited by (12)

  • Enantioselective synthesis of HIV protease inhibitor amprenavir via Co-catalyzed HKR of 2-(1-azido-2-phenylethyl)oxirane

    2012, Tetrahedron Asymmetry
    Citation Excerpt :

    The strategy employed herein mainly comprises the Co-catalyzed HKR of racemic azido epoxide 11 as the key chirality inducing step. We expect this methodology to find a wide use for the synthesis of other similar HEA multifunctional HIV protease inhibitors.14 Solvents were purified and dried by standard procedures prior to use.

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