Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
68751 | Journal of Molecular Catalysis A: Chemical | 2006 | 7 Pages |
A procedure for obtaining increased selectivity in a diastereoselective double ring-closing metathesis reaction is presented. The key to success was design of a substrate, which directed the reaction mechanism through a selective pathway and use of a suitable catalyst combination to achieve the desired balance between reactivity and selectivity.
Graphical abstractA procedure for obtaining increased selectivity in a diastereoselective double ring-closing metathesis reaction is presented. The key to success was design of a substrate, which directed the reaction mechanism through a selective pathway and use of a suitable catalyst combination to achieve the desired balance between reactivity and selectivity. Figure optionsDownload full-size imageDownload as PowerPoint slide