An Efficient Stereoselective Total Synthesis of All Stereoisomers of the Antibiotic Thiamphenicol through Ruthenium-Catalyzed Asymmetric Reduction by Dynamic Kinetic Resolution

2015 ◽  
Vol 2015 (27) ◽  
pp. 5949-5958 ◽  
Author(s):  
Marc Perez ◽  
Pierre-Georges Echeverria ◽  
Elsa Martinez-Arripe ◽  
Mehdi Ez Zoubir ◽  
Ridha Touati ◽  
...  
2019 ◽  
Vol 2 (1) ◽  
Author(s):  
Saima Perveen ◽  
Shuang Yang ◽  
Miao Meng ◽  
Weici Xu ◽  
Guoxiang Zhang ◽  
...  

2007 ◽  
Vol 349 (4-5) ◽  
pp. 617-628 ◽  
Author(s):  
Fumihiko Saitoh ◽  
Hidemitsu Nishida ◽  
Takafumi Mukaihira ◽  
Kohsuke Aikawa ◽  
Koichi Mikami

2021 ◽  
Author(s):  
Fuzhuo Li ◽  
Li-Cheng Yang ◽  
Jingyang Zhang ◽  
Jason Chen ◽  
Hans Renata

We report a biocatalytic transamination method to prepare a broad range of b-branched a-amino acids that proceeds with high diastereo- and enantioselectivity. Mechanistic studies show that the transformation proceeds through a dynamic kinetic resolution process that is unique to the optimal enzyme. To highlight its utility and practicality, the biocatalytic reaction is applied to the synthesis of several cyclic fragments and in the first total synthesis of jomthonic acid A.


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