Chiral amine–imine ligands based on trans-2,5-disubstituted pyrrolidines and their application in the palladium-catalyzed allylic alkylation

2009 ◽  
Vol 20 (14) ◽  
pp. 1672-1682 ◽  
Author(s):  
Hongfeng Chen ◽  
James A. Sweet ◽  
Kin-Chung Lam ◽  
Arnold L. Rheingold ◽  
Dominic V. McGrath
2009 ◽  
Vol 28 (15) ◽  
pp. 4464-4474 ◽  
Author(s):  
M. Rosa Axet ◽  
Francesco Amoroso ◽  
Giovanni Bottari ◽  
Angela D’Amora ◽  
Ennio Zangrando ◽  
...  

2019 ◽  
Vol 23 (11) ◽  
pp. 1168-1213 ◽  
Author(s):  
Samar Noreen ◽  
Ameer Fawad Zahoor ◽  
Sajjad Ahmad ◽  
Irum Shahzadi ◽  
Ali Irfan ◽  
...  

Background: Asymmetric catalysis holds a prestigious role in organic syntheses since a long time and chiral inductors such as ligands have been used to achieve the utmost desired results at this pitch. The asymmetric version of Tsuji-Trost allylation has played a crucial role in enantioselective synthesis. Various chiral ligands have been known for Pdcatalyzed Asymmetric Allylic Alkylation (AAA) reactions and exhibited excellent catalytic potential. The use of chiral ligands as asymmetric inductors has widened the scope of Tsuji-Trost allylic alkylation reactions. Conclusion: Therefore, in this review article, a variety of chiral inductors or ligands have been focused for palladium catalyzed asymmetric allylic alkylation (Tsuji-Trost allylation) and in this regard, recently reported literature (2013-2017) has been described. The use of ligands causes the induction of enantiodiscrimination to the allylated products, therefore, the syntheses of various kinds of ligands have been targeted by many research groups to employ in Pd-catalyzed AAA reactions.


1986 ◽  
Vol 51 (4) ◽  
pp. 421-426 ◽  
Author(s):  
Tetsuo Tsuda ◽  
Masahiro Okada ◽  
Seiichi Nishi ◽  
Takeo Saegusa

Synlett ◽  
2007 ◽  
Vol 2007 (10) ◽  
pp. 1521-1524
Author(s):  
David Madec ◽  
Giovanni Poli ◽  
Mathieu Thuong ◽  
Silvia Sottocornola ◽  
Guillaume Prestat ◽  
...  

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