Intermediates in nucleophilic aromatic substitution. XII. Kinetic and equilibrium study of the spiro Meisenheimer complex of 1(.beta.-hydroxyethoxy)-2,4-dinitrobenzene

1974 ◽  
Vol 39 (8) ◽  
pp. 1054-1058 ◽  
Author(s):  
Claude F. Bernasconi ◽  
Heide S. Cross

Author(s):  
Kjell Jorner ◽  
Tore Brinck ◽  
Per-Ola Norrby ◽  
David Buttar

Hybrid reactivity models, combining mechanistic calculations and machine learning with descriptors, are used to predict barriers for nucleophilic aromatic substitution.



Synlett ◽  
2020 ◽  
Author(s):  
Xiaohua Liu ◽  
Yi Li ◽  
Hao Pan ◽  
Wang-Yuren Li ◽  
Xiaoming Feng

AbstractAn asymmetric organocatalytic nucleophilic aromatic substitution reaction of azlactones with electron-deficient aryls was established. A variety of α-aryl α-alkyl α-amino acid esters and peptides were obtained in decent yields and stereoselectivities. A new bifunctional catalytic mode involving charge-transfer interaction and hydrogen bonding is proposed to explain the enantioselectivity.



2007 ◽  
pp. 2264 ◽  
Author(s):  
Masahiro Ueno ◽  
Misato Yonemoto ◽  
Masahiro Hashimoto ◽  
Andrew E. H. Wheatley ◽  
Hiroshi Naka ◽  
...  


Synlett ◽  
2013 ◽  
Vol 24 (19) ◽  
pp. 2575-2580 ◽  
Author(s):  
Takashi Matsumoto ◽  
Yuuki Fujimoto ◽  
Ryohei Itakura ◽  
Hiroki Hoshi ◽  
Hikaru Yanai ◽  
...  


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