ChemInform Abstract: Catalytic Asymmetric Conjugate Addition of Isocyanoacetate to (Z)-3-Substituted-2-(4-pyridyl)-acrylonitrile, a Reactive Class of Michael Acceptor.

ChemInform ◽  
2016 ◽  
Vol 47 (22) ◽  
Author(s):  
Claudia Del Fiandra ◽  
Maria Moccia ◽  
Valentina Cerulli ◽  
Mauro F. A. Adamo
2016 ◽  
Vol 52 (8) ◽  
pp. 1697-1700 ◽  
Author(s):  
Claudia Del Fiandra ◽  
Maria Moccia ◽  
Valentina Cerulli ◽  
Mauro F. A. Adamo

Un-substituted isocyanoacetate ethyl ester reacted with Michael acceptors 1a–m under the catalysis of Cinchona based quaternary ammonium salts providing imines 4a–m as a single diastereoisomer and in up to 94% ees.


ChemInform ◽  
2015 ◽  
Vol 46 (45) ◽  
pp. no-no
Author(s):  
Nilanjana Majumdar ◽  
Akira Saito ◽  
Liang Yin ◽  
Naoya Kumagai ◽  
Masakatsu Shibasaki

2019 ◽  
Vol 84 (12) ◽  
pp. 7829-7839 ◽  
Author(s):  
Jin-Rong Wang ◽  
Xiao-Li Jiang ◽  
Qing-Qing Hang ◽  
Shu Zhang ◽  
Guang-Jian Mei ◽  
...  

2017 ◽  
Vol 8 (1) ◽  
pp. 641-646 ◽  
Author(s):  
Zhenbo Gao ◽  
Stephen P. Fletcher

Synthetic methods for the selective formation of all carbon quaternary centres in non-cyclic systems are rare. Here we report highly enantioselective Cu-catalytic asymmetric conjugate addition of alkylzirconium species to twelve different acyclic trisubstituted enones.


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