Assignment of Absolute Configuration of Natural Abundance Deuterium Signals Associated with (R)- and (S)-Enantioisotopomers in a Fatty Acid Aligned in a Chiral Liquid Crystal:  Enantioselective Synthesis and NMR Analysis

2006 ◽  
Vol 128 (34) ◽  
pp. 11180-11187 ◽  
Author(s):  
Vincent Baillif ◽  
Richard J. Robins ◽  
Isabelle Billault ◽  
Philippe Lesot
Synlett ◽  
1989 ◽  
Vol 1989 (1) ◽  
pp. 18-19 ◽  
Author(s):  
Kazuo Yamamura ◽  
Satoru Ono ◽  
Hisanobu Ogoshi ◽  
Hideki Masuda ◽  
Yasuhisa Kuroda

Synlett ◽  
1989 ◽  
Vol 1989 (01) ◽  
pp. 18-19 ◽  
Author(s):  
Kazuo Yamamura ◽  
Satoru Ono ◽  
Hisanobu Ogoshi ◽  
Hideki Masuda ◽  
Yasuhisa Kuroda

Author(s):  
B.D. Terris ◽  
R. J. Twieg ◽  
C. Nguyen ◽  
G. Sigaud ◽  
H. T. Nguyen

We have used a force microscope in the attractive, or noncontact, mode to image a variety of surfaces. In this mode, the microscope tip is oscillated near its resonant frequency and shifts in this frequency due to changes in the surface-tip force gradient are detected. We have used this technique in a variety of applications to polymers, including electrostatic charging, phase separation of ionomer surfaces, and crazing of glassy films.Most recently, we have applied the force microscope to imaging the free surfaces of chiral liquid crystal films. The compounds used (Table 1) have been chosen for their polymorphic variety of fluid mesophases, all of which exist within the temperature control range of our force microscope.


2020 ◽  
Vol 23 (26) ◽  
pp. 2960-2968
Author(s):  
Renáta Kertiné Ferenczi ◽  
Tünde-Zita Illyés ◽  
Sándor Balázs Király ◽  
Gyula Hoffka ◽  
László Szilágyi ◽  
...  

The reported enantioselective synthesis for the preparation of (+)-(2R,3R)-2-(4- hydroxy-3-methoxyphenyl)-3-hydroxymethyl-1,4-benzodioxane-6-carbaldehyde, precursor for the stereoselective synthesis of bioactive flavanolignans, could not be reproduced. Thus, the target molecule was prepared via the synthesis and separation of diastereomeric O-glucosides. TDDFT-ECD calculations and the 1,4-benzodioxane helicity rule were utilized to determine the absolute configuration. ECD calculations also confirmed that the 1Lb Cotton effect is governed by the helicity of the heteroring, while the higher-energy ECD transitions reflect mainly the orientation of the equatorial C-2 aryl group.


2021 ◽  
Author(s):  
Eryn Nelson ◽  
Jeffrey S. S. K. Formen ◽  
Christian Wolf

The widespread occurrence and significance of chiral compounds does not only require new methods for their enantioselective synthesis but also efficient tools that allow rapid determination of the absolute configuration,...


2013 ◽  
Vol 572 (1) ◽  
pp. 59-65 ◽  
Author(s):  
M. Infusino ◽  
A. De Luca ◽  
F. Ciuchi ◽  
A. Ionescu ◽  
N. Scaramuzza ◽  
...  

2012 ◽  
Vol 116 (15) ◽  
pp. 8678-8687 ◽  
Author(s):  
Daiki Tsuji ◽  
Yoichi Takanishi ◽  
Jun Yamamoto ◽  
Atsushi Yoshizawa

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