Ab Initio SCF and DFT Studies on Solvent Effects on Intramolecular Rearrangement Reactions

2001 ◽  
Vol 105 (17) ◽  
pp. 4272-4283 ◽  
Author(s):  
Pratim K. Chattaraj ◽  
Patricia Pérez ◽  
Jenny Zevallos ◽  
Alejandro Toro-Labbé
2004 ◽  
Vol 686 (1-3) ◽  
pp. 83-89 ◽  
Author(s):  
K. Anandan ◽  
P. Kolandaivel ◽  
R. Kumaresan

1981 ◽  
Vol 36 (11) ◽  
pp. 1356-1360 ◽  
Author(s):  
Dieter Bentmann ◽  
Uwe Klingebiel

Abstract Halogenosilanes, with the exception of CH3SiF3 and SiF4, react with lithiated bis-(trimethylsilyl)hydroxylamine in ether to yield substituted hydroxylamines, and LiF. In the analogous reaction with trifluoromethylsilane and tetrafluorosilane the products undergo an intramolecular rearrangement to form silylaminosiloxanes.


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