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A New Stereochemical Model from NMR for Benzoylated Cyclodextrins, Promising New Chiral Solvating Agents for the Chiral Analysis of 3,5-Dinitrophenyl Derivatives

✍ Scribed by Uccello-Barretta, Gloria; Cuzzola, Angela; Balzano, Federica; Menicagli, Rita; Iuliano, Anna; Salvadori, Piero


Book ID
120658476
Publisher
American Chemical Society
Year
1997
Tongue
English
Weight
380 KB
Volume
62
Category
Article
ISSN
0022-3263

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πŸ“œ SIMILAR VOLUMES


Benzoylated and Benzylated Cyclodextrins
✍ Gloria Uccello-Barretta; Angela Cuzzola; Federica Balzano; Rita Menicagli; Piero πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 279 KB πŸ‘ 2 views

Benzoylated and benzylated cyclodextrins give rise to non-spectroscopy. Cyclodextrins bearing aromatic substituents at the primary or secondary sites only are more efficient CSAs equivalence in the 1 H-NMR spectra of racemates of 3,5dinitrophenyl derivatives of chiral amines, amino alcohols, compare

N-(n-Butylamide) of (S)-2-(phenylcarbamo
✍ Dario Pini; Gloria Uccello-Barretta; Carlo Rosini; Piero Salvadori πŸ“‚ Article πŸ“… 1991 πŸ› John Wiley and Sons 🌐 English βš– 252 KB

The N-(n-butylamide) of (S)-2-(phenylcarbamoyloxy)propionic acid, easily prepared starting from the inexpensive L-ethyl lactate, can be used as convenient chiral solvating agent (CSA) to determine the enantiomeric composition of N-(3,5-dinitrobenzoyl)amino acid methyl esters.