Chromatographic optical resolution on trans‐1,2‐diaminocyclohexane derivatives: Theory and applications
- 1 January 1992
- Vol. 4 (7), 447-458
- https://doi.org/10.1002/chir.530040709
Abstract
No abstract availableKeywords
This publication has 14 references indexed in Scilit:
- Chiral α‐substituted α‐aryloxy acetic acids: Synthesis, absolute configuration, chemical resolution, and direct separation by hplcChirality, 1992
- Enantiomeric separation of substituted 2-aryloxy propionic esters : Application to the determination of the enantiomeric excess in herbicide formulationsJournal of Chromatography A, 1991
- Chromatographic resolution of 1,2-amino alcohols on a chiral stationary phase containing N,N′-(3,5-dinitrobenzoyl)-trans-1,2-diaminocyclohexane : Theoretical and practical aspectsJournal of Chromatography A, 1991
- Direct resolution of racemic compounds on chiral microbore columns by sub‐ and supercritical fluid chromatographyJournal of High Resolution Chromatography, 1990
- Chapter 34 Significance of Drug Stereochemistry in Modern Pharmaceutical Research and DevelopmentPublished by Elsevier ,1990
- Synthesis of (2R) and (2S)-benzyl-2,3-epoxypropyl ether from a common precursor: O-benzyl-L-serineTetrahedron Letters, 1989
- C2 symmetry and asymmetric inductionChemical Reviews, 1989
- Considerations of chiral recognition relevant to the liquid chromatography separation of enantiomersChemical Reviews, 1989
- High-performance liquid chromatography on chiral packed microbore columns with the 3,5-dinitrobenzoyl derivative of trans-1,2-diaminocyclohexane as selectorJournal of Chromatography A, 1988
- The Preparation, Separation, and Characterization of the lel3- and ob3-Isomers of Tris(trans-1,2-cyclohexanediamine)rhodium(III) Complexes.Acta Chemica Scandinavica, 1972