A Novel Synthesis of Cyclohexylnorstatine Isopropyl Ester, the C-Terminal Component of a Renin Inhibitor

Heterocycles ◽  
1990 ◽  
Vol 30 (1) ◽  
pp. 299 ◽  
Author(s):  
Shiro Terashima ◽  
Yoshio Ito ◽  
Tetsuhide Kamijo ◽  
Hiromu Harada
2018 ◽  
Author(s):  
Guangbin Dong ◽  
Renhe Li

Herein, we describe our initial development of an asymmetric Pd-catalyzed annulation between aryl iodides and racemic epoxides for synthesis of 2,3-dihydrobenzofurans using a chiral norbornene cocatalyst. A series of enantiopure ester-, amide- and imide-substituted norbornenes have been prepared with a reliable synthetic route. Promising enantioselectivity (42-45% ee) has been observed using the isopropyl ester-substituted norbornene (N1*) and the amide-substituted norbornene (N7*).


2000 ◽  
Author(s):  
Thorsten Schroer ◽  
Karl O. Christe
Keyword(s):  

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