| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5228899 | Tetrahedron | 2008 | 7 Pages |
Abstract
The intermolecular reductive coupling of aromatic imines with acylimidazoles was effected by electroreduction in the presence of chlorotrimethylsilane and gave α-amino-α-aryl ketones. This method was also effective for the synthesis of α-amino-α-aryl esters using methoxycarbonylimidazole as an electrophile.
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Authors
Naoki Kise, Shinji Morimoto,