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The reaction of dimethyltitanocene with N-substituted-β-lactams
✍ Scribed by Isamir Martı́nez; Amy R Howell
- Publisher
- Elsevier Science
- Year
- 2000
- Tongue
- French
- Weight
- 144 KB
- Volume
- 41
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
2-Methyleneazetidines have been synthesized and isolated by the reaction of b-lactams with dimethyltitanocene, followed by chromatography on deactivated silica. Ecient conversion required that the lactam nitrogen be strongly deactivated. Methyl transfer predominated in reactions with phenyl and benzyl on the lactam nitrogen.
📜 SIMILAR VOLUMES
Regioselective halogenation of the N-susbtituted lactams (3a)-(3d) affords the corresponding exocyclic bromides (4a)-(4d). The procedure provides a novel alternative mute to N-(c&aloaJkyl)-substituted lactams, which are of particular interest in the synthesis of g-lactam antibiotics. Reactions of N