| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5278941 | Tetrahedron Letters | 2007 | 4 Pages |
Abstract
In tandem ring-closing metathesis of alkynyl silaketals containing two different tethered olefins, the gem-dimethyl group showed the expected Thorpe-Ingold effect, thereby giving good level of group selectivity. Unexpectedly, however, the corresponding gem-diphenyl group did not show any Thorpe-Ingold effect for the ring-closure reaction.
Graphical abstractDownload full-size image
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Yi Jin Kim, Jonathan B. Grimm, Daesung Lee,
