C–H hyperconjugation in alkyl benzene cations as revealed by position‐dependent isotope effects on nonradiative decay rates of electron donor–acceptor complexes

1980 ◽  
Vol 73 (7) ◽  
pp. 3512-3514 ◽  
Author(s):  
S. Okajima ◽  
Bee T. Lim ◽  
E. C. Lim
Keyword(s):  
Electron Donor ◽  
Isotope Effects ◽  
Decay Rates ◽  
Alkyl Benzene ◽  
Nonradiative Decay ◽  
Donor Acceptor

Hydrogen isotope effects in electron donor-acceptor systems

1979 ◽  
Vol 20 (31) ◽  
pp. 2919-2920 ◽  
Author(s):  
F.M. Martens ◽  
J.W. Verhoeven ◽  
Th.J. de Boer
Keyword(s):  
Electron Donor ◽  
Hydrogen Isotope ◽  
Isotope Effects ◽  
Donor Acceptor

Metal-Free Photoinduced Hydroalkylation Cascade Enabled by an Electron-Donor-Acceptor Complex

2020 ◽  
Author(s):  
José Tiago Menezes Correia ◽  
Gustavo Piva da Silva ◽  
Camila Menezes Kisukuri ◽  
Elias André ◽  
Bruno Pires ◽  
...  
Keyword(s):  
Electron Donor ◽  
Functional Group ◽  
Photoexcited Electron ◽  
One Pot ◽  
Quaternary Centers ◽  
Metal Free ◽  
Acceptor Complex ◽  
Catalyst Free ◽  
Donor Acceptor ◽  
Radical Cascade

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>.

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