Enantiomeric recognition of organic ammonium salts by chiral crown ethers based on the pyridino-18-crown-6 structure

1984 ◽  
Vol 49 (2) ◽  
pp. 353-357 ◽  
Author(s):  
Richard B. Davidson ◽  
Jerald S. Bradshaw ◽  
Brian A. Jones ◽  
N. Kent Dalley ◽  
James J. Christensen ◽  
...  
Keyword(s):  
Crown Ethers ◽  
Ammonium Salts ◽  
Chiral Crown Ethers ◽  
Enantiomeric Recognition

ChemInform Abstract: ENANTIOMERIC RECOGNITION OF ORGANIC AMMONIUM SALTS BY CHIRAL CROWN ETHERS BASED ON THE PYRIDINO-18-CROWN-6 STRUCTURE

1984 ◽  
Vol 15 (25) ◽  
Author(s):  
R. B. DAVIDSON ◽  
J. S. BRADSHAW ◽  
B. A. JONES ◽  
N. K. DALLEY ◽  
J. J. CHRISTENSEN ◽  
...  
Keyword(s):  
Crown Ethers ◽  
Ammonium Salts ◽  
Chiral Crown Ethers ◽  
Enantiomeric Recognition

Novel C1-symmetric chiral crown ethers bearing rosin acids groups: synthesis and enantiomeric recognition for ammonium salts

Tetrahedron ◽  
2014 ◽  
Vol 70 (50) ◽  
pp. 9545-9553 ◽  
Author(s):  
Lu-zhi Liu ◽  
Chun-huan He ◽  
Lin Yang ◽  
Yan Huang ◽  
Qiang Wu ◽  
...  
Keyword(s):  
Crown Ethers ◽  
Ammonium Salts ◽  
Chiral Crown Ethers ◽  
Rosin Acids ◽  
Enantiomeric Recognition

scholarly journals Synthesis, Molecular Recognition Study and Liquid Membrane-Based Applications of Highly Lipophilic Enantiopure Acridino-Crown Ethers

Molecules ◽  
2020 ◽  
Vol 25 (11) ◽  
pp. 2571
Author(s):  
Ádám Golcs ◽  
Bálint Árpád Ádám ◽  
Viola Horváth ◽  
Tünde Tóth ◽  
Péter Huszthy
Keyword(s):  
Crown Ethers ◽  
Liquid Membrane ◽  
Structural Features ◽  
Amino Acid Derivatives ◽  
Electrochemical Studies ◽  
Model Compounds ◽  
Guest Molecules ◽  
Enantiomeric Recognition ◽  
Sensor Molecules ◽  
Phase Transport

New highly lipophilic enantiopure crown ethers containing a heterocyclic unit have been synthesized. Phase transport, UV-Vis- and fluorescence spectrophotometric investigations as well as electrochemical studies on the complexation of the new macrocycles with several amine and amino acid derivatives were also carried out. Achiral amines were used for studying the structural preference of the new macrocycles. Among the studied structural features of the guest molecules, the intermolecular π-π interaction showed the most significant effect on complexation, which made the aralkylamine-type compounds the most preferable guest molecules. The studied liquid membrane-based applications and photophysical investigations showed appreciable enantiomeric recognition toward some aralkylamine model compounds with homochiral preferences. New crown ether derivatives (R,R)-2 and (S,S)-2 were successfully applied as enantioselective carrier and sensor molecules.

ChemInform Abstract: Macroheterocycles. Part 33. Binuclear Chiral Crown Ethers.

ChemInform ◽  
1988 ◽  
Vol 19 (24) ◽  
Author(s):  
N. G. LUK'YANENKO ◽  
A. V. LOBACH ◽  
L. N. LYAMTSEVA ◽  
N. YU. NAZAROVA ◽  
L. P. KARPENKO
Keyword(s):  
Crown Ethers ◽  
Chiral Crown Ethers

Enantiomeric differentiation of racemic organic salts by chiral crown ethers derived from sugars

1986 ◽  
Vol 51 (10) ◽  
pp. 1906-1908 ◽  
Author(s):  
Denis Gehin ◽  
Pierre Di Cesare ◽  
Bernard Gross
Keyword(s):  
Crown Ethers ◽  
Organic Salts ◽  
Chiral Crown Ethers
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