Six closely related cyclic phosphoric acids (1a‐f) were compared with respect to their resolving ability towards ephedrine. Variation of the aromatic substituent in the phosphoric acids significantly influences this ability. Studying the results of the resolution experiments as a function of some physico‐chemical properties of the diastereomeric salts reveals a relationship between the resolving ability of a particular phosphoric acid and the difference in heat of fusion of its diastereomeric salts
(1) (R)-(+)-4-(2,6-Dichlorophenyl)-2-hydroxy-5,5-dimethyl-1,3,2-dioxaphosphorinane 2-oxide (1S,2R)-(...
The optical resolution processes were systematically investigated. The optimum of the parameters of ...
( S)-1-Phenyl-2-( p-tolyl)ethylamine ( S)-1, used for the industrial scale resolution of chrysanthem...
Six closely related cyclic phosphoric acids (1a‐f) were compared with respect to their resolving abi...
The crystal structures of two pairs of diastereomeric salts consisting of ephedrine and a cyclic pho...
The effects of various aromatic substituents in both ephedrine and a cyclic phosphoric acid on the q...
Detailed structural studies of five pairs of diastereomeric salts of ephedrine and halogen-substitut...
The possibility of solid solution behavior of diastereomeric salts, containing multiple resolving ag...
Diastereomeric salt resolution is still the most relevant technique in chiral resolution processes, ...
NoCrystal structure prediction simulations were carried out to explore the solid state packing alter...
AbstractA screening of crystallization conditions for the diastereomeric salts formed by L/D-malic a...
An insight into the mechanism of the highly e cient resolution of 1-phenylethylamine with enantiomer...
The crystallization and resolution of cis-permethric acid (cPA) with (1R)-1-phenylethanamine (PhEA) ...
This paper presents an experimental and modelling approach to understanding the key conditions for d...
Contains fulltext : 32893.pdf (publisher's version ) (Closed access
(1) (R)-(+)-4-(2,6-Dichlorophenyl)-2-hydroxy-5,5-dimethyl-1,3,2-dioxaphosphorinane 2-oxide (1S,2R)-(...
The optical resolution processes were systematically investigated. The optimum of the parameters of ...
( S)-1-Phenyl-2-( p-tolyl)ethylamine ( S)-1, used for the industrial scale resolution of chrysanthem...
Six closely related cyclic phosphoric acids (1a‐f) were compared with respect to their resolving abi...
The crystal structures of two pairs of diastereomeric salts consisting of ephedrine and a cyclic pho...
The effects of various aromatic substituents in both ephedrine and a cyclic phosphoric acid on the q...
Detailed structural studies of five pairs of diastereomeric salts of ephedrine and halogen-substitut...
The possibility of solid solution behavior of diastereomeric salts, containing multiple resolving ag...
Diastereomeric salt resolution is still the most relevant technique in chiral resolution processes, ...
NoCrystal structure prediction simulations were carried out to explore the solid state packing alter...
AbstractA screening of crystallization conditions for the diastereomeric salts formed by L/D-malic a...
An insight into the mechanism of the highly e cient resolution of 1-phenylethylamine with enantiomer...
The crystallization and resolution of cis-permethric acid (cPA) with (1R)-1-phenylethanamine (PhEA) ...
This paper presents an experimental and modelling approach to understanding the key conditions for d...
Contains fulltext : 32893.pdf (publisher's version ) (Closed access
(1) (R)-(+)-4-(2,6-Dichlorophenyl)-2-hydroxy-5,5-dimethyl-1,3,2-dioxaphosphorinane 2-oxide (1S,2R)-(...
The optical resolution processes were systematically investigated. The optimum of the parameters of ...
( S)-1-Phenyl-2-( p-tolyl)ethylamine ( S)-1, used for the industrial scale resolution of chrysanthem...