| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5276700 | Tetrahedron Letters | 2011 | 4 Pages |
Abstract
Primary and secondary silylated alcohols are easily converted to bis(methoxyphenyl)methyl (BMPM) ethers in good yields using CuBr2 as catalyst in acetonitrile at room temperature. Various other protecting groups are compatible with this mild and convenient process.
Graphical abstractPrimary and secondary silylated alcohols are easily and rapidly converted to bis(methoxyphenyl)methyl (BMPM) ethers in good yields using CuBr2 as catalyst in acetonitrile at room temperature. Various other protecting groups are compatible with this mild and convenient process.Download full-size image
Related Topics
Physical Sciences and Engineering
Chemistry
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Authors
Simon Specklin, Florian Gallier, Rofia Mezaache, Hassina Harkat, Yénimégué Albert Dembelé, Jean-Marc Weibel, Aurélien Blanc, Patrick Pale,