HPLC Separation of Enantiomers on a Chiral Stationary Phase Containing 1,1′-Bianthracene-2,2′-dicarboxylic Acid Bonded to Silica Gel

1990 ◽  
Vol 19 (1) ◽  
pp. 59-62 ◽  
Author(s):  
Shuichi Ôi ◽  
Masayuki Shijo ◽  
Sotaro Miyano
Keyword(s):  
Stationary Phase ◽  
Dicarboxylic Acid ◽  
Silica Gel ◽  
Chiral Stationary Phase ◽  
Hplc Separation ◽  
Separation Of Enantiomers

Preparation of (R)-(-)-6,6'-Bis(3,5-dinitrobenzamido)biphenyl-2,2'-dicarboxylic Acid, a Potential Chiral HPLC Selector

1995 ◽  
Vol 60 (12) ◽  
pp. 2161-2164 ◽  
Author(s):  
Miloš Tichý ◽  
Jiří Závada
Keyword(s):  
Stationary Phase ◽  
Dicarboxylic Acid ◽  
Chiral Stationary Phase ◽  
Optically Active ◽  
Chiral Hplc ◽  
Hplc Separation ◽  
Separation Of Enantiomers

The title optically active diacid I has been prepared as a potential selector for chiral stationary phase in the HPLC separation of enantiomers.

scholarly journals γ-Cyclodextrin metal–organic framework for efficient separation of chiral aromatic alcohols

RSC Advances ◽  
2017 ◽  
Vol 7 (58) ◽  
pp. 36297-36301 ◽  
Author(s):  
Cheng-Xiong Yang ◽  
Yu-Zhen Zheng ◽  
Xiu-Ping Yan
Keyword(s):  
Stationary Phase ◽  
Chiral Stationary Phase ◽  
Metal Organic Framework ◽  
Hplc Separation ◽  
Efficient Separation ◽  
Aromatic Alcohols ◽  
Metal Organic ◽  
Organic Framework

A γ-cyclodextrin metal–organic framework was applied as an efficient chiral stationary phase for HPLC separation of chiral aromatic alcohols.

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