Citation: A. Iuliano et al., (S)-leucine and [(S)-1-(1-naphthyl)ethyl]amine as chiral building blocks for a bifunctional system - Synthesis of a new chiral stationary phase and evaluation of its biselector properties in the HPLC resolution of racemic compounds, EUR J ORG C, (18), 2001, pp. 3523-3529
Authors:
Iuliano, A
Bartalucci, D
Uccello-Barretta, G
Balzano, F
Salvadori, P
Citation: A. Iuliano et al., 3,5-dinitrobenzoylphenylglycine analogues bearing the 1,1 '-binaphthalene moiety - Synthesis, conformational study, and application as chiral solvating agents, EUR J ORG C, (11), 2001, pp. 2177-2184
Citation: A. Iuliano et al., A circular dichroism approach to the conformation of 1-arylethylamino-substituted 1,3,5-triazine derivatives, EUR J ORG C, (9), 2000, pp. 1767-1772
Authors:
Iuliano, A
Uccello-Barretta, G
Salvadori, P
Citation: A. Iuliano et al., 1-Arylethylamino-substituted s-triazine derivatives as chiral solvating agents for the determination of the enantiomeric composition of chiral compounds, TETRAHEDR-A, 11(7), 2000, pp. 1555-1563
Citation: A. Iuliano et al., Synthesis of a new family of four deoxycholic acid derived chiral stationary phases and their evaluation in the HPLC resolution of racemic compounds, TETRAHEDR-A, 10(17), 1999, pp. 3353-3364
Citation: A. Iuliano et al., The s-triazine chromophore as a probe for the absolute configuration determination of (+)-1-(9-anthryl)ethylamine by circular dichroism, J ORG CHEM, 64(16), 1999, pp. 5754-5756
Authors:
Uccello-Barretta, G
Iuliano, A
Franchi, E
Balzano, F
Salvadori, P
Citation: G. Uccello-barretta et al., Di- and tri-1-(1-naphthyl)ethylamino-substituted 1,3,5-triazine derivatives: A new class of versatile chiral auxiliaries for NMR spectroscopy, J ORG CHEM, 63(25), 1998, pp. 9197-9203
Authors:
Iuliano, A
Franchi, E
Uccello-Barretta, G
Salvadori, P
Citation: A. Iuliano et al., Circular dichroism determination of the conformation of optically pure 1-(1-naphthyl)ethylamino-substituted 1,3,5-triazine derivatives, J ORG CHEM, 63(24), 1998, pp. 8765-8768