Solvent- and Achiral-Guest-Triggered Chiral Inversion in a Planar Chiralpseudo[1]Catenane

2013 ◽  
Vol 125 (31) ◽  
pp. 8269-8273 ◽  
Author(s):  
Tomoki Ogoshi ◽  
Tomohiro Akutsu ◽  
Daiki Yamafuji ◽  
Takamichi Aoki ◽  
Tada-aki Yamagishi
Keyword(s):  
Author(s):  
Penghua Qin ◽  
Zhen Wu ◽  
Pengyu Li ◽  
Dian Niu ◽  
Minghua Liu ◽  
...  

2017 ◽  
Vol 76 (7) ◽  
pp. 1816-1826 ◽  
Author(s):  
Luong N. Nguyen ◽  
Faisal I. Hai ◽  
James A. McDonald ◽  
Stuart J. Khan ◽  
William E. Price ◽  
...  

This study demonstrates continuous enantiomeric inversion and further biotransformation of chiral profens including ibuprofen, naproxen and ketoprofen by an enzymatic membrane bioreactor (EMBR) dosed with laccase. The EMBR showed non-enantioselective transformations, with high and consistent transformation of both (R)- and (S)-ibuprofen (93 ± 6%, n= 10), but lower removals of both enantiomers of naproxen (46 ± 16%, n= 10) and ketoprofen (48 ± 17%, n= 10). Enantiomeric analysis revealed a bidirectional but uneven inversion of the profens, for example 14% inversion of (R)- to (S)- compared to 4% from (S)- to (R)-naproxen. With redox-mediator addition, the enzymatic chiral inversion of both (R)- and (S)-profens remained unchanged, although the overall conversion became enantioselective; except for (S)-naproxen, the addition of redox mediator promoted the degradation of (R)-profens only.


Chirality ◽  
1990 ◽  
Vol 2 (2) ◽  
pp. 74-78 ◽  
Author(s):  
Sylvia Müller ◽  
Joachim M. Mayer ◽  
Jean-Claude Etter ◽  
Bernard Testa

Soft Matter ◽  
2017 ◽  
Vol 13 (17) ◽  
pp. 3072-3075 ◽  
Author(s):  
Yizhi Liu ◽  
Xinpei Gao ◽  
Fei Lu ◽  
Mei Hu ◽  
Lijuan Shi ◽  
...  

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