| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5277555 | Tetrahedron Letters | 2006 | 4 Pages |
Abstract
An efficient synthesis of ortho-substituted triphenolamines via reductive amination is reported. This approach allows access to this increasingly important class of ligands in a structurally systematic way using either commercially or easily synthesizable building blocks.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Leonard J. Prins, Myriam Mba Blázquez, Andrej KolaroviÄ, Giulia Licini,