Abstract:
A diastereoselective (de 80–92%) synthesis of α-amino phosphonates was accomplished by reaction of diethyl phosphite sodium salt with 3-R-1-phenyl-2,3-dihydro-1H-naphth[1,2-e]-[1,3]oxazines being the products of aminoacetalization of aldehydes with 1-(α-aminobenzyl)-2-naphthol (Betti base).
Citation:
K. A. Nikitina, K. E. Metlushka, D. N. Sadkova, L. N. Shaimardanova, V. A. Alfonsov, “Synthesis of α-amino phosphonates by diastereoselective addition of diethyl phosphite sodium salt to aldimines derived from Betti base”, Mendeleev Commun., 26:5 (2016), 395–396
Linking options:
https://www.mathnet.ru/eng/mendc2224
https://www.mathnet.ru/eng/mendc/v26/i5/p395
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