| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5286960 | Tetrahedron Letters | 2005 | 4 Pages |
Abstract
Glycine-derived N-tosyl-5,5-divinyloxazolidin-2-one 10 undergoes a palladium catalysed decarboxylative ring-opening cyclization with strongly electron deficient alkylidenemalonate derivatives to give highly substituted pyrrolidines 14 containing two contiguous quaternary centres.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
![Synthesis of highly substituted pyrrolidines via palladium catalysed formal [2+3] cycloaddition of 5-vinyloxazolidin-2-ones to activated alkenes](/preview/png/5286960.png "First Page Preview: Synthesis of highly substituted pyrrolidines via palladium catalysed formal [2+3] cycloaddition of 5-vinyloxazolidin-2-ones to activated alkenes")
Authors
Julian G. Knight, Kirill Tchabanenko, Paul A. Stoker, Simon J. Harwood,