A stereoselective two step sequence for the construction of fused pyrrolidone ring systems has been developed which features the intramolecular [3+2] dipolar cycloaddition of unsaturated azomethine ylides. The ylides are produced upon reaction of aminomethylphosphonates with so-olefimic aldehydes, f
โฆ LIBER โฆ
Intramolecular cycloadditions with azomethine ylides for the synthesis of metacyclophanes
โ Scribed by W. Eberbach; H. Fritz; I. Heinze; P. von Laer; P. Link
- Publisher
- Elsevier Science
- Year
- 1986
- Tongue
- French
- Weight
- 248 KB
- Volume
- 27
- Category
- Article
- ISSN
- 0040-4039
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โฆ Synopsis
On thermal treatment of the aziridines Sa-f intramolecular cycloaddition reactions of the intermedsteazomethine ylides 6 result in the formation of the metacyclophanes L-9. FoF 7a and 7b the conformational barriers are estimated to-be app';;;ximatzy 20 and 12 kcal/mol, respectively.
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