Comparison of (R)-(-)-6,6'-Bis(3,5-dinitrobenzamido)biphenyl-2,2'-dicarboxylic and (S)-(+)-6,6'-Bis-(3,5-dinitrobenzamidomethyl)biphenyl-2,2'-dicarboxylic Acids as Chiral HPLC Selectors

1997 ◽  
Vol 62 (1) ◽  
pp. 62-68 ◽  
Author(s):  
Miloš Tichý ◽  
Luděk Ridvan ◽  
Jiří Závada

The title optically active diacids (R)-I and (S)-II of known absolute configuration were investigated as selectors in HPLC separation of enantiomers. With a standard set of benzamido alcohols and biaryl compounds, the separation was less efficient and less general than that found for selectors based on studied previously.

1995 ◽  
Vol 60 (12) ◽  
pp. 2161-2164 ◽  
Author(s):  
Miloš Tichý ◽  
Jiří Závada

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


Chirality ◽  
2009 ◽  
Vol 21 (6) ◽  
pp. 604-612 ◽  
Author(s):  
Roberto Cirilli ◽  
Rosella Ferretti ◽  
Francesco La Torre ◽  
Anna Borioni ◽  
Vincenzo Fares ◽  
...  

Tetrahedron ◽  
2003 ◽  
Vol 59 (43) ◽  
pp. 8589-8595 ◽  
Author(s):  
Tiina Putkonen ◽  
Arto Tolvanen ◽  
Reija Jokela ◽  
Salvatore Caccamese ◽  
Nunziatina Parrinello

ChemInform ◽  
2004 ◽  
Vol 35 (10) ◽  
Author(s):  
Tiina Putkonen ◽  
Arto Tolvanen ◽  
Reija Jokela ◽  
Salvatore Caccamese ◽  
Nunziatina Parrinello

ChemInform ◽  
2010 ◽  
Vol 30 (33) ◽  
pp. no-no
Author(s):  
Masanobu Yamamoto ◽  
Hiroyuki Yamazawa ◽  
Naoto Nakajima ◽  
Tetsu Ando

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