A highly effective H-1 NMR method for determining the absolute configurations of various chiral a-hydroxyl acids and their derivatives has been developed with the use of bisthioureas (R)-CSA 1 and (S)-CSA 1 as chiral solvating agents in the presence of DABCO, giving distinguishable proton signals with up to 0.66 ppm chemical shift nonequivalence. Computational modeling studies were performed with Gaussian09 to reveal the chiral recognition mechanism
A rapid and the simple chiral derivatizing protocol involving the coupling of 2-formylphenylboronic ...
Three-component chiral derivatization protocols are proposed for the assignment of the absolute conf...
In the present PhD project new chiral solvating agents (CSAs) have been proposed for the differentia...
A highly effective <sup>1</sup>H NMR method for determining the absolute configurations of various c...
The utility of enantiopure BINOL (1,10-Bi-2-naphthol), in a ternary ion-pair complex, which is obtai...
A simple strategy for configurational assignments of alpha-amino acids has been developed by compari...
A simple strategy for configurational assignments of alpha-amino acids has been developed by compari...
A simple strategy for configurational assignments of alpha-amino acids has been developed by compari...
A simple strategy for configurational assignments of alpha-amino acids has been developed by compari...
A simple chiral bisthiourea has been used as a highly effective and practical chemical solvating age...
The reaction of benzoyl isothiocyanate with (1R,2R)-1,2-bis(2-hydroxyphenyl)ethylenediamine afforded...
Thiourea chiral solvating agents (CSA) for the NMR enantiodiscrimination of chiral substrates have b...
Enantiomers of a few new amides containing two stereogenic centers have been derived from D- and L-α...
In the field of chiral recognition, reported chiral discrimination by 1H NMR spectroscopy has mainly...
A rapid and the simple chiral derivatizing protocol involving the coupling of 2-formylphenylboronic ...
A rapid and the simple chiral derivatizing protocol involving the coupling of 2-formylphenylboronic ...
Three-component chiral derivatization protocols are proposed for the assignment of the absolute conf...
In the present PhD project new chiral solvating agents (CSAs) have been proposed for the differentia...
A highly effective <sup>1</sup>H NMR method for determining the absolute configurations of various c...
The utility of enantiopure BINOL (1,10-Bi-2-naphthol), in a ternary ion-pair complex, which is obtai...
A simple strategy for configurational assignments of alpha-amino acids has been developed by compari...
A simple strategy for configurational assignments of alpha-amino acids has been developed by compari...
A simple strategy for configurational assignments of alpha-amino acids has been developed by compari...
A simple strategy for configurational assignments of alpha-amino acids has been developed by compari...
A simple chiral bisthiourea has been used as a highly effective and practical chemical solvating age...
The reaction of benzoyl isothiocyanate with (1R,2R)-1,2-bis(2-hydroxyphenyl)ethylenediamine afforded...
Thiourea chiral solvating agents (CSA) for the NMR enantiodiscrimination of chiral substrates have b...
Enantiomers of a few new amides containing two stereogenic centers have been derived from D- and L-α...
In the field of chiral recognition, reported chiral discrimination by 1H NMR spectroscopy has mainly...
A rapid and the simple chiral derivatizing protocol involving the coupling of 2-formylphenylboronic ...
A rapid and the simple chiral derivatizing protocol involving the coupling of 2-formylphenylboronic ...
Three-component chiral derivatization protocols are proposed for the assignment of the absolute conf...
In the present PhD project new chiral solvating agents (CSAs) have been proposed for the differentia...