Highly diastereoselective synthesis of functionalized β-lactams

Article abstract of DOI:10.1080/00397919708006088

An efficient method based, on the acid chloride-imine reaction, is reported for the preparation of 1,3-disubstituted β-lactams in good yield and with high selectivity.

Full text of DOI:10.1080/00397919708006088

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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Highly Diastereoselective
Synthesis of Functionalized β-
Lactams
Djillali Ait Sidhouma a & Hadj Benhaoua a b
a Institut de ChimieUniversité, Oran Es-senia, Algeria
b Université de Rennes I, Groupe de Recherche de
Physicochimie Structurale 3, associté au CNRS.
Avenue du Général Leclerc, F-35042, Rennes, France
Published online: 22 Aug 2006.
To cite this article: Djillali Ait Sidhouma & Hadj Benhaoua (1997) Highly
Diastereoselective Synthesis of Functionalized β-Lactams, Synthetic Communications:
An International Journal for Rapid Communication of Synthetic Organic Chemistry,
27:9, 1519-1525, DOI: 10.1080/00397919708006088
To link to this article: http://dx.doi.org/10.1080/00397919708006088
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