Publication | Open Access
Synthesis of the peptidic α-hydroxy amides phebestin, probestin, and bestatin from α-keto amide precursors
34
Citations
20
References
1999
Year
Bioorganic ChemistryOrganic ChemistryPeptide ScienceChemical BiologyPharmaceutical ChemistryMolecular PharmacologyMedicinal ChemistryAminopeptidase InhibitorsZinc BorohydrideProtein Degradationα-Keto Amide PrecursorsInhibitory ActivityBiochemistryBioconjugationPharmacologyNatural Product SynthesisNatural SciencesPeptide SynthesisMedicineSynthetic ChemistryDrug Discovery
Aminopeptidase inhibitors, phebestin, probestin and bestatin have been prepared by stereospecific reduction of α-keto amide precursors using zinc borohydride.
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