Ab initio molecular orbital and photoelectron spectroscopic study of the pyridine–boron trifluoride electron-donor–acceptor complex

1988 ◽  
Vol 84 (4) ◽  
pp. 409-415 ◽  
Author(s):  
Ian H. Hillier ◽  
Mark A. Vincent ◽  
Joseph A. Connor ◽  
Martyn F. Guest ◽  
Alastair A. MacDowell ◽  
...  
Keyword(s):  
Spectroscopic Study ◽  
Ab Initio ◽  
Molecular Orbital ◽  
Electron Donor ◽  
Boron Trifluoride ◽  
Acceptor Complex ◽  
Donor Acceptor

UVPES and ab Initio Molecular Orbital Studies on the Electron Donor−Acceptor Complexes of Bromine with Methylamines†

1997 ◽  
Vol 101 (6) ◽  
pp. 1155-1159 ◽  
Author(s):  
S. Salai Cheettu Ammal ◽  
S. P. Ananthavel ◽  
P. Venuvanalingam
Keyword(s):  
Ab Initio ◽  
Molecular Orbital ◽  
Electron Donor ◽  
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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