1992
DOI: 10.1515/znb-1992-0411
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Darstellung von 1,3,5-Trimethyl-4,6-dioxo-1,3,5,2λ3-triazaphosphinanen; Einkristall-Röntgenstrukturanalyse eines Platin(II)-Komplexes/Preparation of 1,3,5-Trimethyl-4,6-dioxo-1,3,5,2λ3-triazaphosphinanes; Single Crystal X-Ray Diffraction Study of a Platinum(II)-Complex

Abstract: 1,3,5-Trimethylbiuret, 1,3,5-Trimethyl-4,6-dioxo-1,3,5,2/.3-triazaphosphinane, X-Ray, Staudinger Reaction A new synthesis for 2-chloro-l,3,5-trim ethyl-4,6-dioxo-l,3,5,2A3-triazaphosphinane (1) is described. Chlorine-fluorine exchange in 1 by means o f sodium fluoride in acetonitrile in the presence of catalytic am ounts of a crown ether furnished 2-fluoro-l, 3,5-trimethyl-4,6-dioxol,3,5,2A3-triazaphosphinane (2). The synthesis of the bromine and iodine analogues, 3 and 4, by metathesis of 1 with the appropria… Show more

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Cited by 14 publications
(2 citation statements)
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“…It is thus probable that these derivatives and the azole antifungal compounds, such as ketoconazole or itraconazole possess a similar mechanism of action at molecular level. 7,8 Materials and Methods Elemental analyses were done by combustion with a Carlo Erba Instrument or gravimetrically for the metal ions. Electronic spectra have been recorded at room temperature on a VSU-2G spectrophotometer Dichlorotetramorpholino-cyclophosphazatriene using MgO as standard material.…”
Section: +mentioning
confidence: 99%
See 1 more Smart Citation
“…It is thus probable that these derivatives and the azole antifungal compounds, such as ketoconazole or itraconazole possess a similar mechanism of action at molecular level. 7,8 Materials and Methods Elemental analyses were done by combustion with a Carlo Erba Instrument or gravimetrically for the metal ions. Electronic spectra have been recorded at room temperature on a VSU-2G spectrophotometer Dichlorotetramorpholino-cyclophosphazatriene using MgO as standard material.…”
Section: +mentioning
confidence: 99%
“…Synthesis of complexes of dichloro-tetramorpholino-cyclophosphazatriene (L) [1][2][3][4][5][6][7] All complexes have been synthesised according to the following general procedure: methanolic solutions containing the metal salts MX2.nH20 (M Co, Ni, Mn; X C1, AcO) and the ligand (L) were mixed with stirring in 1" 1, 2"1 and 3:2 molar ratios of M L. The resulting mixtures were refluxed for 60 min on a water bath. The complexes were separated by filtration, washed with diethylether and dried in a dessicator (on (13205)2).…”
Section: +mentioning
confidence: 99%