Chiral resolution of racemic etiracetam was achieved via co-crystallization with ZnCl2. Depending on the amount of ZnCl2 either a stable racemic compound or a stable conglomerate can be obtained. Excess ZnCl2 triggers the quantitative conversion of the racemate into the conglomerate solid; this unprecedented behaviour was investigated through a racetam/ZnCl2/solvent phase diagram.

Solid-state chiral resolution mediated by stoichiometry: Crystallizing etiracetam with ZnCl2 / Shemchuk, Oleksii; Song, Lixing; Robeyns, Koen; Braga, Dario; Grepioni, Fabrizia*; Leyssens, Tom. - In: CHEMICAL COMMUNICATIONS. - ISSN 1359-7345. - STAMPA. - 54:77(2018), pp. 10890-10892. [10.1039/c8cc06199h]

Solid-state chiral resolution mediated by stoichiometry: Crystallizing etiracetam with ZnCl2

Shemchuk, Oleksii;Braga, Dario;Grepioni, Fabrizia
;
2018

Abstract

Chiral resolution of racemic etiracetam was achieved via co-crystallization with ZnCl2. Depending on the amount of ZnCl2 either a stable racemic compound or a stable conglomerate can be obtained. Excess ZnCl2 triggers the quantitative conversion of the racemate into the conglomerate solid; this unprecedented behaviour was investigated through a racetam/ZnCl2/solvent phase diagram.
2018
Solid-state chiral resolution mediated by stoichiometry: Crystallizing etiracetam with ZnCl2 / Shemchuk, Oleksii; Song, Lixing; Robeyns, Koen; Braga, Dario; Grepioni, Fabrizia*; Leyssens, Tom. - In: CHEMICAL COMMUNICATIONS. - ISSN 1359-7345. - STAMPA. - 54:77(2018), pp. 10890-10892. [10.1039/c8cc06199h]
Shemchuk, Oleksii; Song, Lixing; Robeyns, Koen; Braga, Dario; Grepioni, Fabrizia*; Leyssens, Tom
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/661728
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