In an embodiment, a composition including a chiral solvating agent to resolve nuclear magnetic resonance signals of an enantiomer of at least one analyte, where the chiral solvating agent facilitates in the at least one analyte binding to a C.sub.2 face or a C.sub.3 face of the chiral solvating agent, and where the chiral solvating agent causes an upfield shift or a downfield shift in at least one nuclear magnetic resonance signals corresponding to a .sup.1H, .sup.19F{.sup.1H}, or .sup.31P{.sup.1H} signal, and where the chiral solvating agent includes a cobalt cation. In another embodiment, a method that includes mixing a chiral solvating agent, including a cobalt cation, with at least one analyte to form a solution, obtaining nuclear magne...
Quantification and identification of chiral drugs and their metabolites constitutes a significant i...
International audienceStudies of the perturbing effect of chiral solvating agents (CSAs) 5a and most...
The use of 2,4,6-tri[(S)-1%-methylbenzylamino]-1,3,5-triazine as a chiral solvating agent for the NM...
This chapter will focus on the use of chiral solvating agents (CSAs) for the detection and quantific...
Two enantiomers of chiral drugs often show different pharmaceutical activities.1 Consequently, the s...
This chapter will describe the general features and main categories of chiral solvating agents (CSAs...
The manuscript reports two novel ternary ion-pair complexes, which serve as chiral solvating agents,...
The utility of <sup>13</sup>C NMR spectroscopy for the differentiation of enantiomers using chiral s...
Cyclic tetraamidic chiral selectors are efficient chiral solvating agents (CSAs) for NMR spectroscop...
A summary of selected NMR studies of enantiodiscrimination phenomena regarding the use of quinine-ba...
The utility of enantiopure BINOL (1,10-Bi-2-naphthol), in a ternary ion-pair complex, which is obtai...
Chiral molecules possess enantiomers that have non-superimposable chemical structures but exhibit id...
Chiral analysis, such as determination of identity, concentration, and relative ratio of optically a...
In the field of chiral recognition, reported chiral discrimination by 1H NMR spectroscopy has mainly...
Recently, we have described the synthesis of chiral metal–organic frameworks iPr-ChirUMCM-1 and Bn-C...
Quantification and identification of chiral drugs and their metabolites constitutes a significant i...
International audienceStudies of the perturbing effect of chiral solvating agents (CSAs) 5a and most...
The use of 2,4,6-tri[(S)-1%-methylbenzylamino]-1,3,5-triazine as a chiral solvating agent for the NM...
This chapter will focus on the use of chiral solvating agents (CSAs) for the detection and quantific...
Two enantiomers of chiral drugs often show different pharmaceutical activities.1 Consequently, the s...
This chapter will describe the general features and main categories of chiral solvating agents (CSAs...
The manuscript reports two novel ternary ion-pair complexes, which serve as chiral solvating agents,...
The utility of <sup>13</sup>C NMR spectroscopy for the differentiation of enantiomers using chiral s...
Cyclic tetraamidic chiral selectors are efficient chiral solvating agents (CSAs) for NMR spectroscop...
A summary of selected NMR studies of enantiodiscrimination phenomena regarding the use of quinine-ba...
The utility of enantiopure BINOL (1,10-Bi-2-naphthol), in a ternary ion-pair complex, which is obtai...
Chiral molecules possess enantiomers that have non-superimposable chemical structures but exhibit id...
Chiral analysis, such as determination of identity, concentration, and relative ratio of optically a...
In the field of chiral recognition, reported chiral discrimination by 1H NMR spectroscopy has mainly...
Recently, we have described the synthesis of chiral metal–organic frameworks iPr-ChirUMCM-1 and Bn-C...
Quantification and identification of chiral drugs and their metabolites constitutes a significant i...
International audienceStudies of the perturbing effect of chiral solvating agents (CSAs) 5a and most...
The use of 2,4,6-tri[(S)-1%-methylbenzylamino]-1,3,5-triazine as a chiral solvating agent for the NM...