Publication | Closed Access
Synthesis of Peptides Containing α,α‐Disubstituted α‐Amino Acids by the Azirine/Oxazolone Method: The (12–20)‐Nonapeptide of the Ionophore Alamethicin
60
Citations
41
References
1990
Year
Bioorganic ChemistryIonophore AlamethicinPeptide EngineeringPeptides Containing αOrganic ChemistryPeptide SciencePharmaceutical Chemistry‐Nonapeptide Z‐leu‐aib‐pro‐val‐aib‐aib‐gluBiochemistryIonophor AlamethicinDiversity-oriented SynthesisAzirine/oxazolone MethodPharmacologyNatural Product SynthesisBiomolecular EngineeringNatural SciencesPeptide SynthesisMedicineSynthetic ChemistryH ‐Azirines 2
Abstract The (12–20)‐nonapeptide Z‐Leu‐Aib‐Pro‐Val‐Aib‐Aib‐Glu (OBzl)‐Gln‐Pheol ( 10 ) of the ionophor alamethicin was synthesized by a new strategy, using 3‐amino‐2,2‐dimethyl‐2 H ‐azirines 2 as synthons for the α‐aminoisobutyric acid (Aib) moieties.
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