103345-86-4Relevant articles and documents
[1-Hydroxy-1-(2-hydroxyphenyl)ethyl]phosphonates and -phosphinates: Convenient synthesis through intramolecular Abramov reaction and protective activity against influenza A
Korshin, Edward E.,Pozdeev, Oskar K.
, p. 11109 - 11115 (2014/01/06)
A combination of intramolecularization and tandem reaction methodologies has been applied to the synthesis of diethylammonium[1-hydroxy-1-(2- hydroxyphenyl)ethyl]phosphonates and -phosphinates, which were found to be unavailable through a standard intermolecular hydrophosphonylation/hydrolysis sequence. A mild hydrolysis of amidophosphites and -phosphonites, bearing 2-acetylphenoxy-fragment and a hydrolytically labile diethylamino-group at the same trivalent phosphorus atom, directly afforded the title compounds. The overall process probably consists of three steps: (i) selective hydrolysis of the P(III)-N bond to generate the hydrophosphoryl-type intermediates; (ii) formation of the strained 2-substituted 3-hydroxy-2-oxo-2,3-dihydro-1,2- benzoxaphospholes through intramolecular Abramov reaction; (iii) hydrolysis of the endocyclic P(IV)-O bond in the 1,2-benzoxaphospholes to give the acyclic products. Being only modestly active in vitro, at high dosage non-toxic water-soluble title α,γ-dihydroxyphosphonates and -phosphinates exhibited beneficial, but short-lasting effect against experimental influenza A infection (H3N2) in mice.
PHOSPHORYLATION OF o-HYDROXYACETOPHENONE BY PHOSPHORUS ACID CHLORIDES IN THE PRESENCE OF A BASE
Mukhametov, F. S.,Korshin, E. E.
, p. 1788 - 1794 (2007/10/02)
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