| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5220293 | Tetrahedron | 2011 | 9 Pages |
Abstract
A new variant of the Reformatsky–Claisen rearrangement is described. The reaction of substituted allyl α-bromoacetates with indium and indium(III) chloride under ultrasonication provides a general entry into the functionalized synthon.
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