Nondynamic and Dynamic Kinetic Resolution of Lactones with Stereogenic Centers and Axes:  Stereoselective Total Synthesis of Herbertenediol and Mastigophorenes A and B†

2000 ◽  
Vol 122 (38) ◽  
pp. 9127-9133 ◽  
Author(s):  
Gerhard Bringmann ◽  
Thomas Pabst ◽  
Petra Henschel ◽  
Jürgen Kraus ◽  
Karl Peters ◽  
...  
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

2015 ◽  
Vol 2015 (27) ◽  
pp. 5949-5958 ◽  
Author(s):  
Marc Perez ◽  
Pierre-Georges Echeverria ◽  
Elsa Martinez-Arripe ◽  
Mehdi Ez Zoubir ◽  
Ridha Touati ◽  
...  

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.


2014 ◽  
Vol 50 (83) ◽  
pp. 12526-12529 ◽  
Author(s):  
Mu-Wang Chen ◽  
Xian-Feng Cai ◽  
Zhang-Pei Chen ◽  
Lei Shi ◽  
Yong-Gui Zhou

An efficient and facile route to chiral tetrahydroquinolines with three contiguous stereogenic centers via a dynamic kinetic resolution process has been successfully developed by using chiral phosphoric acid as catalyst and Hantzsch ester as the hydrogen source with up to 89% ee.


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