1965
DOI: 10.1039/jr9650005032
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923. Phosphorus–nitrogen compounds. Part XVI. The reactions of hexachlorocyclotriphosphazatriene with t-butylamine

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Cited by 50 publications
(28 citation statements)
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“…The product 7 showed a singlet in the 31 P NMR spectrum. 18,19 The characteristic signal of N 3 P 3 Cl 6 at 21.1 ppm is shifted to 11.3 ppm, providing direct evidence for the obtained product. 31 P NMR indicates that all chlorine atoms of hexachlorocyclotriphosphazene were replaced by methyl 4-(3-amino-hexadecahydro-7-hydroxy-10,13-dimethyl-1H-cyclopenta[a]phenanthren-17-yl)-pentanoate substituent.…”
Section: Nmr Spectramentioning
confidence: 91%
“…The product 7 showed a singlet in the 31 P NMR spectrum. 18,19 The characteristic signal of N 3 P 3 Cl 6 at 21.1 ppm is shifted to 11.3 ppm, providing direct evidence for the obtained product. 31 P NMR indicates that all chlorine atoms of hexachlorocyclotriphosphazene were replaced by methyl 4-(3-amino-hexadecahydro-7-hydroxy-10,13-dimethyl-1H-cyclopenta[a]phenanthren-17-yl)-pentanoate substituent.…”
Section: Nmr Spectramentioning
confidence: 91%
“…Furthermore we observe that the ratio geminal to non-geminal products increases by using acetonitrile as a solvent instead of diethylether. The enhanced yield of NPAm2NPCl2NSOPh can be ascribed either to a mechanism involving an hydrogen bridged transition state [8] or to a proton abstraction mechanism [9]. Both processes are obviously favoured in the presence of the solvent acetonitrile.…”
Section: Eis -Isomermentioning
confidence: 98%
“…Aminochlorocyclotriphosphazatrienes were prepared by literature methods [3][4][5][6][7][8][9][10][11][12]. Light petroleum, b.p.…”
Section: Methodsmentioning
confidence: 99%