Hydroxypyridyl Imines: Enhancing Chromatographic Separation and Stereochemical Analysis of Chiral Amines via Circular Dichroism

2016 ◽  
Vol 81 (18) ◽  
pp. 8199-8205 ◽  
Author(s):  
Leo A. Joyce ◽  
Erik L. Regalado ◽  
Christopher J. Welch
2012 ◽  
Vol 134 (9) ◽  
pp. 4398-4407 ◽  
Author(s):  
Justin M. Dragna ◽  
Gennaro Pescitelli ◽  
Lee Tran ◽  
Vincent M. Lynch ◽  
Eric V. Anslyn ◽  
...  

Chirality ◽  
2017 ◽  
Vol 30 (1) ◽  
pp. 29-42 ◽  
Author(s):  
Marcin Górecki ◽  
Maria Annunziata M. Capozzi ◽  
Gianluigi Albano ◽  
Cosimo Cardellicchio ◽  
Lorenzo Di Bari ◽  
...  

Chirality ◽  
2010 ◽  
pp. NA-NA ◽  
Author(s):  
Christian Merten ◽  
Karl J. Jalkanen ◽  
Volker C. Weiss ◽  
Andreas Hartwig

2019 ◽  
Vol 15 ◽  
pp. 1913-1924 ◽  
Author(s):  
Bartosz Setner ◽  
Agnieszka Szumna

Directional self‐assembly of conformationally well-defined complexes in polar environment is still a major challenge in supramolecular chemistry. In the present study we demonstrate that resorcin[4]arene sulfonic acid (RSA) interacts with chiral amines (amino acid derivatives and aminocavitands) to form inclusion complexes and capsules based on electrostatic interactions. The complexes were characterized by circular dichroism and DOSY NMR spectroscopy. Chirality transfer from amines onto a resorcinarene skeleton was manifested by the appearance of signals in CD spectra and diastereotopic splitting in NMR spectra. The complexes proved to be thermodynamically stable in methanol, but DMSO and methanol/water mixtures were found to be highly disintegrative for these complexes. This result is quite non-intuitive and worth attention in the context of formation of supramolecular complexes in polar environment, for which DMSO is most often a first-choice solvent.


2017 ◽  
Vol 2017 (16) ◽  
pp. 2338-2343 ◽  
Author(s):  
Liming Chen ◽  
Shanshan Yu ◽  
Meng Xiao ◽  
Zeng Huang ◽  
Kaili Wen ◽  
...  

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