A remarkable chiral recognition of racemic Mosher's acid salt by naturally derived chiral ionic liquids using 19F NMR spectroscopy

RSC Advances ◽  
2016 ◽  
Vol 6 (46) ◽  
pp. 39758-39761 ◽  
Author(s):  
R. Jayachandra ◽  
Sabbasani Rajasekhara Reddy

A new class of d-xylose derived imidazolium-based chiral ionic liquids were designed and synthesized via simple tuning approaches.

2008 ◽  
Vol 61 (7) ◽  
pp. 521 ◽  
Author(s):  
Hong-Shuai Gao ◽  
Zhi-Guo Hu ◽  
Jian-Ji Wang ◽  
Zhao-Fa Qiu ◽  
Feng-Qiu Fan

A novel class of chiral ionic liquids with chiral cations directly derived from natural l-proline has been synthesized and their physical properties such as melting point, thermal degradation, and specific rotation have been characterized. Further, their potential use in chiral recognition was demonstrated by studying interactions with racemic Mosher’s acid salt.


2016 ◽  
Vol 40 (10) ◽  
pp. 8408-8417 ◽  
Author(s):  
Ramisetti Nageswara Rao ◽  
Kondapalli Santhakumar

A 19F NMR spectroscopic method using cyclodextrins as chiral recognition agents was developed for the quantitative determination of emtricitabine enantiomers.


Polymers ◽  
2020 ◽  
Vol 12 (11) ◽  
pp. 2449
Author(s):  
Martyn Dobinson ◽  
Philip Hodge ◽  
Trevor Wear

The capping of “living” poly(methyl methacrylate) (PMMA) and “living” polystyrene (PS), both prepared by the RAFT technique, with various olefins was screened using 19F-NMR spectroscopy. The capping of “living” PMMA with a labeled stilbene was as high as 63% and with certain cinnamate esters was essentially quantitative, but the capping of “living” polystyrene with all the olefins investigated was generally poor.


2015 ◽  
Vol 26 (18-19) ◽  
pp. 1069-1082 ◽  
Author(s):  
Maria Vasiloiu ◽  
Isabella Cervenka ◽  
Peter Gaertner ◽  
Matthias Weil ◽  
Christian Schröder ◽  
...  

2018 ◽  
Vol 52 (7) ◽  
pp. 658-662 ◽  
Author(s):  
S. V. Moiseev ◽  
N. E. Kuz’mina ◽  
V. I. Krylov ◽  
V. A. Yashkir ◽  
V. A. Merkulov

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