Rearrangement of N-allyl-α,α-dichloroamides, β- or γ-functionalized, to substituted analogues of the γ-aminobutyric acid (GABA)

Article abstract of DOI:10.1080/00397919908086013

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

Full text of DOI:10.1080/00397919908086013

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Rearrangement of N-Allyl-α,α-
dichloroamides, β- or γ-
Functionalized, to Substituted
Analogues of the γ-Aminobutyric
Acid (GABA)
Franco Bellesia a , Luca Forti a , Franco Ghelfi a , Gianluca
Ghirardki a , Emanuela Libertini a , Ugo M. Pagnoni a ,
Adriano Pinetti a & Nicola Prochilo a
a Dipartimento di Chimica dell'Universtá , Via Campi 183,
1-41100, Modena, Italy
Published online: 17 Sep 2007.
To cite this article: Franco Bellesia , Luca Forti , Franco Ghelfi , Gianluca Ghirardki ,
Emanuela Libertini , Ugo M. Pagnoni , Adriano Pinetti & Nicola Prochilo (1999) Rearrangement
of N-Allyl-α,α-dichloroamides, β- or γ- Functionalized, to Substituted Analogues of
the γ-Aminobutyric Acid (GABA), Synthetic Communications: An International Journal
for Rapid Communication of Synthetic Organic Chemistry, 29:21, 3739-3748, DOI:
10.1080/00397919908086013
To link to this article: http://dx.doi.org/10.1080/00397919908086013
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