| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1399712 | European Journal of Medicinal Chemistry | 2008 | 4 Pages |
Abstract
Homoclausenamide was synthesized for the first time, and the intramolecular cyclization study of N-methyl-3-phenyl-N-(2-(E)-phenylethenyl)-trans(cis)-oxiranecarboxamide well demonstrated how the stereochemistry affects the cyclization paths.
Graphical abstractUnder Lewis acid condition, compound 8 undergoes cyclizations to give Homoclausenamide and Dehydroclausenamide.Figure optionsDownload full-size imageDownload as PowerPoint slide
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Nianchun Ma, Kemei Wu, Liang Huang,