Stereoselective Crystallization of Chiral 3,4-Dimethylphenyl Glycerol Ether Complicated by Plurality of Crystalline Modifications

Stereoselective Crystallization of Chiral 3,4-Dimethylphenyl Glycerol Ether Complicated by Plurality of Crystalline Modifications

Spontaneous resolution of Pasteur’s salt was historically the first way to obtain pure enantiomers from the racemate. The current increase in interest in the direct racemates resolution during crystallization is largely due to the opened prospects for the industrial application of this app...

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Bibliographic Details
Main Authors: Alexander A. Bredikhin, Dmitry V. Zakharychev, Zemfira A. Bredikhina, Alexey V. Kurenkov, Aida I. Samigullina, Aidar T. Gubaidullin
Format: Article
Language:English
Published: MDPI AG 2020-03-01
Series:Crystals
Subjects:
chirality
deracemization
preferential crystallization
racemic conglomerate
phase behavior
polymorphism
aryl glycerol ethers
Online Access:https://www.mdpi.com/2073-4352/10/3/201

Internet

https://www.mdpi.com/2073-4352/10/3/201

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