Journal of Organic Chemistry
2001-01-01
Asymmetric Synthesis of alpha-Amino Phosphonic Acids by Diastereoselective Addition of Trimethyl Phosphite onto Chiral Oxazolidines(1).
Catherine Maury, Tawfik Gharbaoui, Jacques Royer, Henri-Philippe Husson
文献索引:J. Org. Chem. 61 , 3687, (1996)
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摘要
A simple and general asymmetric synthesis of alpha-amino phosphonic acids is described. The method involves the highly selective addition of trialkyl phosphite onto various chiral oxazolidines. Oxazaphosphorinanes thus obtained with an excellent diastereoselectivity furnish the corresponding (S)-alpha-substituted amino phosphonic acids in good overall yields and high ee (77-->97%) after simple deprotection.
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Micouin, L. et al.
[Tetrahedron Lett. 35 , 7223, (1994)]