Asymmetric organocatalysis – from biomimetic concepts to applications in asymmetric synthesis

2005 ◽  
Vol 2005 (12) ◽  
pp. 8 ◽  
2015 ◽  
Vol 51 (18) ◽  
pp. 3708-3722 ◽  
Author(s):  
Fernanda G. Finelli ◽  
Leandro S. M. Miranda ◽  
Rodrigo O. M. A. de Souza

Despite all the organic chemistry reaction methodologies already developed for the continuous-flow process, asymmetric synthesis is one that has gained less attention.


2021 ◽  
Vol 25 ◽  
Author(s):  
Martina Bortolami ◽  
Francesca Leonelli ◽  
Marta Feroci ◽  
Fabrizio Vetica

: Oxindoles are an important class of heterocyclic scaffolds widely present in natural products and bioactive compounds. For this reason, a plethora of methodologies for the stereoselective synthesis of enantioenriched oxindoles has been studied over the years. Among all the reported synthetic strategies, organocatalysis has proven to be a powerful tool for the asymmetric synthesis of this class of compounds being a step- and atom-economical, environmentally friendly, and non-toxic approach. This review will outline the application of asymmetric organocatalysis in the synthesis of chiral oxindole-based structures, relying on domino/one-pot reaction sequences in a step-economical fashion.


Author(s):  
Yunrong Chen ◽  
Xueqian Ye ◽  
Faqian He ◽  
Xiaoyu Yang

An efficient radical conjugate addition/enantioselective protonation process was developed for the asymmetric synthesis of chiral oxazolines bearing an α-stereocenter through cooperative photoredox catalysis and asymmetric organocatalysis.


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