RT info:eu-repo/semantics/article T1 Synthesis and chromatographic-separation of the stereoisomers of furnidipine A1 Alajarín Ferrández, Luis Ramón A1 Álvarez-Builla Gómez, Julio A1 Vaquero López, Juan J. A1 Sunkel Letelier, Carlos A1 Casa-Juana Muñoz, Miguel Fau de A1 Statkow, Peter R. A1 Sanz-Aparicio, Julia K1 Fumidipine K1 Synthesis K1 Chiral HPLC K1 Four stereoisomers K1 Separation K1 Ciencia K1 Química orgánica K1 Science K1 Chemistry, organic AB The four stereoisomers of methyl tetrahydrofuran-2-ylmethyl 2,6-dimethyl-4-(o-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxilate (furnidipine), have been synthesized and separated by chiral chromatography using D-phenylglycine as chiral stationary phase. Enantiomeric purity of stereoisomers is determined by HPLC-CSP technique and configurations deduced via X-ray crystallography. PB Pergamon SN 0957-4166 YR 1993 FD 1993 LK http://hdl.handle.net/10017/3584 UL http://hdl.handle.net/10017/3584 LA eng DS MINDS@UW RD 29-mar-2024