| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5280819 | Tetrahedron Letters | 2007 | 4 Pages |
Abstract
A bicyclic tetraazatriacetic chelating agent containing a thioalkyl pendant group was prepared. Four synthetic routes have been investigated via a Mitsunobu reaction from 2,4-[bishydroxymethyl]-3-hydroxy-pyridine 1. Deprotection of trityl thioether compound 5c led to ligand 6c in 22% overall yield from the starting 3-hydroxypyridine.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Yi Lin, Alain Favre-Réguillon, Stéphane Pellet-Rostaing, Marc Lemaire,