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Synthesis and biological activity of novel tricyclic β-lactams

✍ Scribed by Stefano Biondi; Giovanni Gaviraghi; Tino Rossi

Publisher
Elsevier Science
Year
1996
Tongue
English
Weight
243 KB
Volume
6
Category
Article
ISSN
0960-894X

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Radical cyclisations of methylenecyclopr
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Addition of lithium bis(methylenecyclopropyl)cuprates to acetoxy azetidinones gives methylenecyclopropyl azetidinones, which can be converted to various radical cyclisation precursors. Attempted 4-exo cyclisation of 3 led only to reduced product, while cyclisation of 5, using CuCl/bipy, gave a carba

ChemInform Abstract: Radical Cyclization
ChemInform Abstract: Radical Cyclizations of Methylenecyclopropyl Azetidinones — Synthesis of Novel Tricyclic β-Lactams.
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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v