| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5280036 | Tetrahedron Letters | 2005 | 4 Pages |
Abstract
Ti(III)-mediated one-electron reduction of phenyldiazonium cation, followed by phenyl radical α-H atom abstraction from ethers, leads to one-pot radical addition of ethers to the C-atom of imines generated in situ from the corresponding aldehydes and imines under aqueous conditions. The reaction is not limited to aromatic aldehydes and may be applied to imines generated in situ from formaldehyde and enolizable aldehydes.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Angelo Clerici, Rosalba Cannella, Walter Panzeri, Nadia Pastori, Eva Regolini, Ombretta Porta,