Carbamoylation at the C(9) site of dihydroquinine affords new and efficient chiral solvating agents for the NMR enantiodiscrimination of simple derivatives of chiral alcohols, amines, carboxyl acids and amino acids
Two enantiomers of chiral drugs often show different pharmaceutical activities.1 Consequently, the s...
The compound (18-crown-6)-2,3,11,12-tetracarboxylic acid was evaluated as a chiral nuclear magnetic ...
Thiourea chiral solvating agents (CSA) for the NMR enantiodiscrimination of chiral substrates have b...
Carbamoyl derivatives of quinine obtained by derivatization of its double bond have been prepared an...
New chiral solvating agents (CSAs) for NMR spectroscopy have been obtained from ethyl (S)-lactate, a...
Several C9-carbamoyl derivatives of quinine have been prepared and compared as chiral solvating agen...
The manuscript reports two novel ternary ion-pair complexes, which serve as chiral solvating agents,...
WOS:000291139700008Four optically active amino alcohols were synthesized via the ring opening of (R)...
This chapter will describe the general features and main categories of chiral solvating agents (CSAs...
Computational and NMR investigations of diastereoisomeric aggregates arising from the interaction of...
Benzoylated and benzylated cyclodextrins give rise to non-equivalence in the 1H-NMR spectra of racem...
The utility of enantiopure BINOL (1,10-Bi-2-naphthol), in a ternary ion-pair complex, which is obtai...
Synthesis and characterization of diamine and aminoalcohol derivatives from isohexides, through ster...
A summary of selected NMR studies of enantiodiscrimination phenomena regarding the use of quinine-ba...
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...
The compound (18-crown-6)-2,3,11,12-tetracarboxylic acid was evaluated as a chiral nuclear magnetic ...
Thiourea chiral solvating agents (CSA) for the NMR enantiodiscrimination of chiral substrates have b...
Carbamoyl derivatives of quinine obtained by derivatization of its double bond have been prepared an...
New chiral solvating agents (CSAs) for NMR spectroscopy have been obtained from ethyl (S)-lactate, a...
Several C9-carbamoyl derivatives of quinine have been prepared and compared as chiral solvating agen...
The manuscript reports two novel ternary ion-pair complexes, which serve as chiral solvating agents,...
WOS:000291139700008Four optically active amino alcohols were synthesized via the ring opening of (R)...
This chapter will describe the general features and main categories of chiral solvating agents (CSAs...
Computational and NMR investigations of diastereoisomeric aggregates arising from the interaction of...
Benzoylated and benzylated cyclodextrins give rise to non-equivalence in the 1H-NMR spectra of racem...
The utility of enantiopure BINOL (1,10-Bi-2-naphthol), in a ternary ion-pair complex, which is obtai...
Synthesis and characterization of diamine and aminoalcohol derivatives from isohexides, through ster...
A summary of selected NMR studies of enantiodiscrimination phenomena regarding the use of quinine-ba...
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...
The compound (18-crown-6)-2,3,11,12-tetracarboxylic acid was evaluated as a chiral nuclear magnetic ...
Thiourea chiral solvating agents (CSA) for the NMR enantiodiscrimination of chiral substrates have b...
DOI
Add to ORKG