A new enantioselective HPLC procedure for the direct resolution of β-amino acids is described, based on the use of a new chiral stationary phase (CSP) containing the macrocyclic glycopeptide antibiotic A-40,926, structurally related to teicoplanin, covalently bonded to silica gel microparticles. The new CSP shows higher enantioselectivity and broader applicability in this field compared to the parent teicoplanin phase. The potential for semi-preparative separations on the A-40,926-CSP is demonstrated for a selected cyclic β-amino acid.
Application of a chiral stationary phase containing the new glycopeptide A-40,926 in the direct chromatographic resolution of beta-amino acids / D'Acquarica, Ilaria; Gasparrini, Francesco; Misiti, Domenico; G., Zappia; C., Cimarelli; G., Palmieri; A., Carotti; S., Cellamare; Villani, Claudio. - In: TETRAHEDRON-ASYMMETRY. - ISSN 0957-4166. - STAMPA. - 11:(2000), pp. 2375-2385. [10.1016/S0957-4166(00)00198-1]
Application of a chiral stationary phase containing the new glycopeptide A-40,926 in the direct chromatographic resolution of beta-amino acids
D'ACQUARICA, Ilaria;GASPARRINI, Francesco;MISITI, Domenico;VILLANI, Claudio
2000
Abstract
A new enantioselective HPLC procedure for the direct resolution of β-amino acids is described, based on the use of a new chiral stationary phase (CSP) containing the macrocyclic glycopeptide antibiotic A-40,926, structurally related to teicoplanin, covalently bonded to silica gel microparticles. The new CSP shows higher enantioselectivity and broader applicability in this field compared to the parent teicoplanin phase. The potential for semi-preparative separations on the A-40,926-CSP is demonstrated for a selected cyclic β-amino acid.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
