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This article is cited in 16 scientific papers (total in 16 papers)
Stereospecific intramolecular cyclization of diethyl (R)-2-(N-benzylidene)-aminobutyl phosphite into (3R,5R)-2-ethoxy-2-oxo-3-phenyl-5-ethyl-1,4,2-oxazaphosphorinane in the presence of hydrogen chloride
M. N. Dimukhametov, E. Yu. Davydova, E. V. Bayandina, A. B. Dobrynin, I. A. Litvinov, V. A. Alfonsov
A.E. Arbuzov Institute of Organic and Physical Chemistry, FRC Kazan Scientific Center of the Russian Academy of Sciences, Kazan, Russian Federation
Abstract:
Diethyl (R)-2-(N-benzylidene)aminobutyl phosphite, formed in reaction of (R)-(+)-2-(N-benzylidene)aminobutan-1-ol with diethyl chlorophosphite, undergoes stereospecific intramolecular cyclization to give P-epimeric (3R,5R)-2-ethoxy-2-oxo-3-phenyl-5-ethyl-1,4,2-oxazaphosphorinanes as final reaction products.
Citation:
M. N. Dimukhametov, E. Yu. Davydova, E. V. Bayandina, A. B. Dobrynin, I. A. Litvinov, V. A. Alfonsov, “Stereospecific intramolecular cyclization of diethyl (R)-2-(N-benzylidene)-aminobutyl phosphite into (3R,5R)-2-ethoxy-2-oxo-3-phenyl-5-ethyl-1,4,2-oxazaphosphorinane in the presence of hydrogen chloride”, Mendeleev Commun., 11:6 (2001), 222–224
Linking options:
https://www.mathnet.ru/eng/mendc4306 https://www.mathnet.ru/eng/mendc/v11/i6/p222
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