2010
DOI: 10.1002/hc.20620
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Synthesis of new functionalized aminomethylphosphonites and their derivatives

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Cited by 68 publications
(11 citation statements)
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“…The double KabachnikeFields condensation made available lipophilic derivatives [15]. The use of phosphorous acid as the P-reactant led to bis(phosphonic acids) [16,17]. Bis(phosphinoxido)derivatives were synthesized via a surprising methylene insertion reaction into a PeN bond followed by oxidation [18].…”
Section: Introductionmentioning
confidence: 99%
“…The double KabachnikeFields condensation made available lipophilic derivatives [15]. The use of phosphorous acid as the P-reactant led to bis(phosphonic acids) [16,17]. Bis(phosphinoxido)derivatives were synthesized via a surprising methylene insertion reaction into a PeN bond followed by oxidation [18].…”
Section: Introductionmentioning
confidence: 99%
“…We realized another interesting route for the synthesis of several aminomethylspirophosphoranes via the interaction of the recently available O,O-diethyl aminomethylphosphonites [13] with ethylene glycol under mild conditions. So, the mixing of the reagents in methylene chloride was accompanied by the rapid formation of hydrogen to give the spirophosphoranes 3, 5, and 6 in high yields (Eq.…”
Section: Resultsmentioning
confidence: 99%
“…The 1 H, 13 C, and 31 P NMR spectra were recorded on a Varian VXR-400 and Bruker Avance-400 spectrometer (400, 100, and 162 MHz, respectively) in C 6 D 6 or CDCl 3 (1)(2)(3)(4)(5)(6)(7)(8)(9)(10)(11)(12)(13)(14)(15)(16)(17)(18). All reactions were carried out under dry argon in anhydrous solvents.…”
Section: Methodsmentioning
confidence: 99%
“…N,N-bis(diethoxyphosphinoylmethyl)-N-methylamine (1e). 18 Following the general procedure, the crude product was purified by preparative GPC using CHCl 3 as eluent to afford a colorless liquid. Yield: 63.7 mg, 77%.…”
Section: Synthesis Of Ammonium Chloride and Ammonium Tetrafluoroboratementioning
confidence: 99%
“…1976, 32, 2089-2098)Prishchenko, A. A.;Livantsov, M. V.; Boganova, N. V.; Lutsenko, I. F. J. Gen. Chem. USSR (Engl.…”
mentioning
confidence: 96%