Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5270840 | Tetrahedron Letters | 2010 | 4 Pages |
Abstract
Chiral phosphinoylimines were prepared from methylphenylphosphonamides and tested as new chiral and activated imines. The addition of aluminum acetylides was proved to be highly diastereoselective while lithium or magnesium acetylides gave poor results. The cleavage of the chiral auxiliary was done under mild conditions and allows the recovery of the starting phosphonamide without loss of optical purity.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Mounira Benamer, Serge Turcaud, Jacques Royer,