A chiral stationary phase with an immobilized, optically active diamine was prepared for the separation of enantiomers. The synthesis of the phase was carried out by bonding (–)trans-1,2-cyclohexanediamine to microparticulate silica gel through the coupling agent 3-glycidoxypropylsilane. The resolution of the racemic compounds catechin, 2,2-dihydroxy-1,1binaphthyl and trans-1,2-cyclohexandiol, is reported

High-performance liquid chromatographic resolution of enantiomers on chiral amine-bonded silica gel / M., Sinibaldi; Carunchio, Vincenzo Tito; C., Corradini; Girelli, Anna Maria. - In: CHROMATOGRAPHIA. - ISSN 0009-5893. - STAMPA. - 18:(1984), pp. 459-462. [10.1007/BF02262978]

High-performance liquid chromatographic resolution of enantiomers on chiral amine-bonded silica gel

CARUNCHIO, Vincenzo Tito;GIRELLI, Anna Maria
1984

Abstract

A chiral stationary phase with an immobilized, optically active diamine was prepared for the separation of enantiomers. The synthesis of the phase was carried out by bonding (–)trans-1,2-cyclohexanediamine to microparticulate silica gel through the coupling agent 3-glycidoxypropylsilane. The resolution of the racemic compounds catechin, 2,2-dihydroxy-1,1binaphthyl and trans-1,2-cyclohexandiol, is reported
1984
Column liquid chromatography; Chiral bonded phase; Racemate resolution
01 Pubblicazione su rivista::01a Articolo in rivista
High-performance liquid chromatographic resolution of enantiomers on chiral amine-bonded silica gel / M., Sinibaldi; Carunchio, Vincenzo Tito; C., Corradini; Girelli, Anna Maria. - In: CHROMATOGRAPHIA. - ISSN 0009-5893. - STAMPA. - 18:(1984), pp. 459-462. [10.1007/BF02262978]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/385268
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