Enantioseparation of 3-Hydroxycarboxylic Acids via Diastereomeric Salt Formation by 2-Amino-1,2-diphenylethanol (ADPE) and Cinchonidine

Enantioseparation of 3-Hydroxycarboxylic Acids via Diastereomeric Salt Formation by 2-Amino-1,2-diphenylethanol (ADPE) and Cinchonidine

Enantioseparation of 3-hydroxycarboxylic acids via diastereomeric salt formation was demonstrated using 2-amino-1,2-diphenylethanol (ADPE) and cinchonidine as the resolving agents. Racemic 3-hydroxy-4-phenylbutanoic acid (<i>rac</i>-<b>1</b>), 3-hydroxy-4-(4-chlorophenyl)buta...

Full description

Bibliographic Details
Main Authors: Srinivas Chandrasekaran, Masaki Tambo, Yuta Yamazaki, Tatsuro Muramatsu, Yusuke Kanda, Takuji Hirose, Koichi Kodama
Format: Article
Language:English
Published: MDPI AG 2022-12-01
Series:Molecules
Subjects:
enantioseparation
diastereomeric salt
3-hydroxycarboxylic acid
chiral recognition
crystal structure
Online Access:https://www.mdpi.com/1420-3049/28/1/114

Internet

https://www.mdpi.com/1420-3049/28/1/114

Similar Items