Characterization of a Chiral Stationary Phase by HR/MAS NMR Spectroscopy and Investigation of Enantioselective Interaction with Chiral Ligates by Transferred NOE

2004 ◽  
Vol 126 (12) ◽  
pp. 3809-3816 ◽  
Author(s):  
Christine Hellriegel ◽  
Urban Skogsberg ◽  
Klaus Albert ◽  
Michael Lämmerhofer ◽  
Norbert M. Maier ◽  
...  
2019 ◽  
Vol 15 ◽  
pp. 1339-1346
Author(s):  
Sven Götz ◽  
Andreas Schneider ◽  
Arne Lützen

The preparative resolution of a trifunctionalized C 3-symmetrical chiral cyclotriveratrylene derivative was achieved via high-performance liquid chromatography (HPLC) on a chiral stationary phase. This approach is a promising alternative to the previously reported resolution through formation of diastereomeric esters because it involves fewer synthetic steps and is less prone to thermal (re)racemization. During these studies an intermediate saddle conformer could also be isolated and characterized by 1H and 13C NMR spectroscopy. The HPLC separation method was further developed in order to allow investigations on the racemization behavior of the cyclotriveratrylene derivative.


2007 ◽  
Vol 353 (3) ◽  
pp. 237-243 ◽  
Author(s):  
Shigeki Matsuya ◽  
Artemis Stamboulis ◽  
Robert G. Hill ◽  
Robert V. Law

2019 ◽  
Vol 21 (23) ◽  
pp. 12576-12584 ◽  
Author(s):  
Bodo Zibrowius ◽  
Michael Felderhoff

Conventional 1D 27Al MAS NMR spectroscopy allows the isotropic chemical shift and the quadrupole coupling parameters of Pnma KAlH4 to be determined precisely.


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