Bull. Russ. Acad. Sci. Div. Chem. Sci. (Engl. Transl.) p. 2096 - 2103 (1992)
Update date:2022-08-02
Topics: Synthesis Oxidation Yield Catalyst Solvent Reduction Nucleophilic substitution Purification Reaction Mechanism Reaction Kinetics Spectroscopic Analysis Tautomerization Stoichiometry Heterocyclic compound Electrophilic addition phosphinate Diazene N-oxide Reaction intermediate Azeotrope
Zlotin, S. G.
Sharashkina, M. V.
Strelenko, Yu. A.
Luk'yanov, O. A.
We have developed a regiospecific method for synthesis of N'-phosphinatodiazene N-oxides, a previously unknown type of azoxy compounds in which the diazene oxide fragment is directly connected with the phosphinate group.The method involves reaction of ami
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Doi:10.1021/jo00126a017
(1995)Doi:10.1016/S0040-4039(00)73871-8
(1993)Doi:10.1016/0223-5234(93)90005-Y
(1993)Doi:10.1134/S1070428013120099
(2013)Doi:10.1016/S0040-4020(99)00297-5
(1999)Doi:10.1016/0040-6031(94)85003-8
(1994)
