Total Synthesis of FR901464. Convergent Assembly of Chiral Components Prepared by Asymmetric Catalysis

2000 ◽  
Vol 122 (42) ◽  
pp. 10482-10483 ◽  
Author(s):  
Christopher F. Thompson ◽  
Timothy F. Jamison ◽  
Eric N. Jacobsen
ChemInform ◽  
2001 ◽  
Vol 32 (10) ◽  
pp. no-no
Author(s):  
Christopher F. Thompson ◽  
Timothy F. Jamison ◽  
Eric N. Jacobsen

2021 ◽  
Vol 25 ◽  
Author(s):  
Hélène Pellissier

: Tandem and domino reactions constitute economic routes to complex molecules starting from simple materials. Especially, combining these powerful procedures to asymmetric catalysis allow a direct access to many elaborated chiral products, including important key intermediates in total syntheses of important biologically active compounds. A range of various types of chiral organocatalysts have already been successfully applied to such syntheses. This review presents major developments in the total synthesis of bioactive products based on the use of enantioselective organocatalytic domino/tandem reactions as key steps. It is divided into three parts, dealing successively with syntheses based on organocatalytic asymmetric Michael-initiated domino reactions as key steps; aldol-initiated domino/tandem reactions and other domino reactions.


2018 ◽  
Vol 5 (23) ◽  
pp. 3402-3405 ◽  
Author(s):  
Jinhong Chen ◽  
Junfang Li ◽  
Longqing Zhu ◽  
Xue Peng ◽  
Yiyue Feng ◽  
...  

Total synthesis and structure revision of chrysamide B are described, the strategy features a convergent assembly of the chiral piperazine core and epoxy-acid.


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