Publication | Open Access
Asymmetric dihydroxylation route to a dipeptide isostere of a protease inhibitor: enantioselective synthesis of the core unit of ritonavir
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Citations
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References
1999
Year
Key StepBiosynthesisProtease InhibitorBiochemistryDipeptide IsostereNatural SciencesMedicineCore UnitOrganic ChemistrySynthetic ChemistryStereoselective SynthesisChemistryPharmacologyAsymmetric CatalysisAsymmetric Dihydroxylation RouteEnantioselective SynthesisDrug DiscoveryNatural Product Synthesis
An enantioselective synthesis of the dipeptide isostere of ritonavir has been accomplished utilizing Sharpless asymmetric hydroxylation as the key step.
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