| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5276032 | Tetrahedron Letters | 2011 | 4 Pages |
Abstract
The dibromocarbene or bromofluorocarbene addition to substituted allyldisilanes afforded instable gem-dibromocyclopropanes or a gem-bromofluorocyclopropane, respectively. These gem-bromohalogenocyclopropanes undergo a spontaneous ring opening at room temperature to give halogenated dienylsilanes or bromo dienes or dibromotetraenes.
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