Parallel synthesis of a small library of hydroxy functionalized bicyclic lactams with optically pure mimicking dipeptide Pro-Ser has been accomplished via aldol condensation of aldehyde 9 with N-BocGlyCO(2)Et. The configurations of eight scaffolds were established unambiguously by NMR spectroscopy

Synthesis of conformationally restricted and optically pure analogues of serine-proline dipeptide via aldolic condensation

Manzoni L;
2004

Abstract

Parallel synthesis of a small library of hydroxy functionalized bicyclic lactams with optically pure mimicking dipeptide Pro-Ser has been accomplished via aldol condensation of aldehyde 9 with N-BocGlyCO(2)Et. The configurations of eight scaffolds were established unambiguously by NMR spectroscopy
2004
Istituto di Scienze e Tecnologie Molecolari - ISTM - Sede Milano
lactams; bicyclic compounds; peptidomimetics; asymmetric synthesis; aldol reaction
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Descrizione: Synthesis of conformationally restricted and optically pure analogues of serine-proline dipeptide via aldol condensation
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/29257
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