| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5278171 | Tetrahedron Letters | 2006 | 4 Pages |
Abstract
1,2-Diphenyl- and 1-phenyl-2-(2-pyridyl)-1,2-disodiumethane efficiently dehalogenate vic-dibromoderivatives, affording the corresponding alkenes. The reaction proceeds rapidly, under mild conditions and is tolerant of a variety of functional groups (alcohol, carboxylic acid, ester and amide). This procedure was successfully extended to similar vic-disubstituted compounds.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Ugo Azzena, Mario Pittalis, Giovanna Dettori, Simona Madeddu, Emanuela Azara,