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JOURNALS // Mendeleev Communications // Archive

Mendeleev Commun., 2016 Volume 26, Issue 5, Pages 395–396 (Mi mendc2224)

This article is cited in 5 papers

Communications

Synthesis of α-amino phosphonates by diastereoselective addition of diethyl phosphite sodium salt to aldimines derived from Betti base

K. A. Nikitinaa, K. E. Metlushkaab, D. N. Sadkovaa, L. N. Shaimardanovaa, V. A. Alfonsova

a A.E. Arbuzov Institute of Organic and Physical Chemistry, FRC Kazan Scientific Center of the Russian Academy of Sciences, Kazan, Russian Federation
b A.M. Butlerov Chemistry Institute, Kazan Federal University, Kazan, Russian Federation

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).

Language: English

DOI: 10.1016/j.mencom.2016.09.009



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