chiral molecular recognition
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2016 ◽  
Vol 23 (6) ◽  
pp. 1273-1277 ◽  
Author(s):  
Akihito Konishi ◽  
Koichi Nakaoka ◽  
Hikaru Maruyama ◽  
Hideto Nakajima ◽  
Tomohiro Eguchi ◽  
...  

2016 ◽  
Vol 52 (69) ◽  
pp. 10540-10543 ◽  
Author(s):  
Ching W. Chan ◽  
Erik Laurini ◽  
Paola Posocco ◽  
Sabrina Pricl ◽  
David K. Smith

We investigate structure–activity effect relationships at the nanoscale chiral molecular recognition interface between enantiomeric self-assembled multivalent (SAMul) systems and biological polyanions, heparin and DNA.


2015 ◽  
Vol 13 (42) ◽  
pp. 10548-10555 ◽  
Author(s):  
Tiina Laaksonen ◽  
Sami Heikkinen ◽  
Kristiina Wähälä

(+)-Dehydroabietylamine (1a), the novel derivatives (2a–6a) and their NTf2 salts (1b–6b) were tested as chiral NMR solvating agents for the resolution of enantiomers of Mosher's acid and other carboxylic acids, and their n-Bu4N salts.


2012 ◽  
Vol 2012 (26) ◽  
pp. 4996-5009 ◽  
Author(s):  
Laura González ◽  
Belén Altava ◽  
Michael Bolte ◽  
M. Isabel Burguete ◽  
Eduardo García-Verdugo ◽  
...  

2009 ◽  
Vol 20 (9) ◽  
pp. 999-1003 ◽  
Author(s):  
Belén Altava ◽  
Dalgi S. Barbosa ◽  
M. Isabel Burguete ◽  
Jorge Escorihuela ◽  
Santiago V. Luis

2007 ◽  
Vol 9 (16) ◽  
pp. 3117-3119 ◽  
Author(s):  
Seiji Shirakawa ◽  
Akihiro Moriyama ◽  
Shoichi Shimizu

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