Internal conversion in 4-substituted 1-naphthylamines. Influence of the electron donor/acceptor substituent character

2000 ◽  
Vol 2 (5) ◽  
pp. 981-991 ◽  
Author(s):  
Kengo Suzuki ◽  
Attila Demeter ◽  
Wolfgang Kühnle ◽  
Erich Tauer ◽  
Klaas A. Zachariasse ◽  
...  
2020 ◽  
Author(s):  
José Tiago Menezes Correia ◽  
Gustavo Piva da Silva ◽  
Camila Menezes Kisukuri ◽  
Elias André ◽  
Bruno Pires ◽  
...  

A metal- and catalyst-free photoinduced radical cascade hydroalkylation of 1,7-enynes has been disclosed. The process is triggered by a SET event involving a photoexcited electron-donor-aceptor complex between NHPI ester and Hantzsch ester, which decomposes to afford a tertiary radical that is readily trapped by the enyne. <a>The method provides an operationally simple, robust and step-economical approach to the construction of diversely functionalized dihydroquinolinones bearing quaternary-centers. A sequential one-pot hydroalkylation-isomerization approach is also allowed giving access to a family of quinolinones. A wide substrate scope and high functional group tolerance was observed in both approaches</a>.


2021 ◽  
Vol 31 (3) ◽  
pp. 326-329
Author(s):  
Olga E. Eremina ◽  
Mariia V. Samodelova ◽  
Mariia V. Ferree ◽  
Tatyana N. Shekhovtsova ◽  
Irina A. Veselova

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