γ-Lactams and furan bispyrrolidines via iodine mediated cyclisation of homoallylamines
Literature Information
Publication Date
2015-08-27
DOI
10.1039/C5QO00183H
Impact Factor
5.281
Authors
Mariwan A. Hama Salih, Louise Male, Neil Spencer, John S. Fossey
View Original
Abstract
1,3,5-Substituted pyrrolidin-2-ones were synthesised via an iodine mediated cyclisation of 3-methyl substituted homoallylamines in good to excellent yield, as mixtures of diastereoisomers. These were separable and their identity confirmed by techniques including single crystal X-ray diffraction. When 3-phenyl substituted homoallylamines were cyclised intriguing fused tricyclic motifs were obtained as C2-symmetric racemates, whose structures were also confirmed by techniques including single crystal X-ray diffraction analysis.
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Source Journal
Organic Chemistry Frontiers
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