Preparation of 2-substituted vinylamino acid derivatives

Article abstract of DOI:10.1080/00397919108021572

Solid-liquid phase transfer catalysis in the absence of any added solvent efficiently promotes Michael addition of glycine Schiff bases to phenylvinylsulfoxide. The vinyl group was formed by thermolysis of the phenylsulfinyl function.

Full text of DOI:10.1080/00397919108021572

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Preparation of 2-Substituted
Vinylamino Acid Derivatives
J. Osuku Opio a , S. Labidalle a , H. Galons a , M.
Miocque a , A. Zaparucha b & A. Loupy b
a Laboratoire de Chimie Organique , Faculté de
Pharmacie , 4, avenue de l'Observatoire, 75270,
Paris, Cedex, 06, France
b Laboratoire des réactions Sélectives sur
Supports, UA CNRS 478 , Université Paris-Sud ,
Bâtiment 410, 91405, Orsay, Cédex, France
Published online: 24 Sep 2006.
To cite this article: J. Osuku Opio , S. Labidalle , H. Galons , M. Miocque ,
A. Zaparucha & A. Loupy (1991) Preparation of 2-Substituted Vinylamino
Acid Derivatives, Synthetic Communications: An International Journal for
Rapid Communication of Synthetic Organic Chemistry, 21:17, 1743-1754, DOI:
10.1080/00397919108021572
To link to this article: http://dx.doi.org/10.1080/00397919108021572
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