Synthesis of methyl 3-amino-3-pyrrolidinecarboxylates: A convenient access to cucurbitine and analogues

Article abstract of DOI:10.1080/00397919508013830

Cycloaddition of N-benzylazomethine ylide 7 to methyl 2-(diphenylmethyleneamino) or 2-(benzylideneamino) acrylates affords the tittle compounds after deprotection by catalytic hydrogenation.

Full text of DOI:10.1080/00397919508013830

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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Synthesis of Methyl 3-Amino-3-
pyrrolidinecarboxylates:
A Convenient Access to
Cucurbitine and Analogues
Omar Mamoun a , Hadj Benhaoua b , Renkeé Danion-
Bougot a & Daniel Danion a
a Groupe de Recherches de Physicochimie
Structurale, U.R.A. C.N.R.S. 704 , Université de
Rennes I , 35042, Rennes Cédex, France
b Institut de Chimie, Laboratoire de Synthèse
Organique, Université d'Oran , Algérie
Published online: 23 Sep 2006.
To cite this article: Omar Mamoun , Hadj Benhaoua , Renkeé Danion-Bougot & Daniel
Danion (1995) Synthesis of Methyl 3-Amino-3-pyrrolidinecarboxylates: A Convenient
Access to Cucurbitine and Analogues, Synthetic Communications: An International
Journal for Rapid Communication of Synthetic Organic Chemistry, 25:9, 1295-1302,
DOI: 10.1080/00397919508013830
To link to this article: http://dx.doi.org/10.1080/00397919508013830
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