This chapter will describe the general features and main categories of chiral solvating agents (CSAs) for NMR spectroscopy, spanning from low-medium sized CSAs to macrocyclic ones. CSAs based on chiral ionic liquids will be introduced, in view of their increasing popularity, and, finally, a short paragraph will be dedicated to special applications of CSAs in particular experimental conditions. Several valuable works, which are mainly devoted to investigate enantiodifferentiation mechanisms by NMR, will not be discussed The main objective is to identify the current trend in the research areas dedicated to the development of new CSAs for NMR spectroscopy
The manuscript reports two novel ternary ion-pair complexes, which serve as chiral solvating agents,...
Chiral recognition is an important subject in various fields including chemistry, biology, pharmaceu...
Carbamoylation at the C(9) site of dihydroquinine affords new and efficient chiral solvating agents ...
This chapter will focus on the use of chiral solvating agents (CSAs) for the detection and quantific...
Cyclic tetraamidic chiral selectors are efficient chiral solvating agents (CSAs) for NMR spectroscop...
Two enantiomers of chiral drugs often show different pharmaceutical activities.1 Consequently, the s...
A summary of selected NMR studies of enantiodiscrimination phenomena regarding the use of quinine-ba...
The utility of <sup>13</sup>C NMR spectroscopy for the differentiation of enantiomers using chiral s...
New chiral solvating agents (CSAs) for NMR spectroscopy have been obtained from ethyl (S)-lactate, a...
In the present PhD project new chiral solvating agents (CSAs) have been proposed for the differentia...
In an embodiment, a composition including a chiral solvating agent to resolve nuclear magnetic reson...
The utility of enantiopure BINOL (1,10-Bi-2-naphthol), in a ternary ion-pair complex, which is obtai...
Quantification and identification of chiral drugs and their metabolites constitutes a significant i...
Chiral auxiliaries are used for NMR spectroscopic study of enantiomers. Often the presence of impuri...
International audienceThe splitting of signals in the NMR spectra originating from enantiotopic site...
The manuscript reports two novel ternary ion-pair complexes, which serve as chiral solvating agents,...
Chiral recognition is an important subject in various fields including chemistry, biology, pharmaceu...
Carbamoylation at the C(9) site of dihydroquinine affords new and efficient chiral solvating agents ...
This chapter will focus on the use of chiral solvating agents (CSAs) for the detection and quantific...
Cyclic tetraamidic chiral selectors are efficient chiral solvating agents (CSAs) for NMR spectroscop...
Two enantiomers of chiral drugs often show different pharmaceutical activities.1 Consequently, the s...
A summary of selected NMR studies of enantiodiscrimination phenomena regarding the use of quinine-ba...
The utility of <sup>13</sup>C NMR spectroscopy for the differentiation of enantiomers using chiral s...
New chiral solvating agents (CSAs) for NMR spectroscopy have been obtained from ethyl (S)-lactate, a...
In the present PhD project new chiral solvating agents (CSAs) have been proposed for the differentia...
In an embodiment, a composition including a chiral solvating agent to resolve nuclear magnetic reson...
The utility of enantiopure BINOL (1,10-Bi-2-naphthol), in a ternary ion-pair complex, which is obtai...
Quantification and identification of chiral drugs and their metabolites constitutes a significant i...
Chiral auxiliaries are used for NMR spectroscopic study of enantiomers. Often the presence of impuri...
International audienceThe splitting of signals in the NMR spectra originating from enantiotopic site...
The manuscript reports two novel ternary ion-pair complexes, which serve as chiral solvating agents,...
Chiral recognition is an important subject in various fields including chemistry, biology, pharmaceu...
Carbamoylation at the C(9) site of dihydroquinine affords new and efficient chiral solvating agents ...