251108-87-9Relevant academic research and scientific papers
Rearrangement of N-allyl-α,α-dichloroamides, β- or γ-functionalized, to substituted analogues of the γ-aminobutyric acid (GABA)
Bellesia, Franco,Forti, Luca,Ghelfi, Franco,Ghirardini, Gianluca,Libertini, Emanuela,Pagnoni, Ugo M.,Pinetti, Adriano,Prochilo, Nicola
, p. 3739 - 3748 (2007/10/03)
The rearrange of γ-chloro, β-hydroxy or β-vinyl N-allyl-N-benzyl- α,α-dichlorocarboxyamides to γ-aminobutyric acid analogues is efficiently promoted by CuCl/N,N,N',N'-tetramethylethylendiamine. With the β-vinyl functionalization a tandem radical-radical r
