The imide-amide rearrangement of trialkyl arylimidophosphates by the action of catalytic amounts of boron trifluoride etherate proceeds at least partially by an intermolecular mechanism.
Synthesis of N,N-disubstituted phosphoramidates via a Lewis acid-catalyzed phosphorimidate rearrangement
作者:Ina Wilkening、Giuseppe del Signore、Christian P. R. Hackenberger
DOI:10.1039/b802030b
日期:——
A Lewis acid-catalyzedrearrangement of phosphorimidates allows a direct, high-yielding transformation of azides with commercially available phosphites into secondary phosphoramidates.
Harger, Martin J. P.; Williams, Andrew, Journal of the Chemical Society. Perkin transactions I, 1986, p. 1681 - 1686
作者:Harger, Martin J. P.、Williams, Andrew
DOI:——
日期:——
Buchanan, G. W.; Morin, F. G.; Fraser, R. R., Canadian Journal of Chemistry, 1980, vol. 58, p. 2442 - 2446
作者:Buchanan, G. W.、Morin, F. G.、Fraser, R. R.
DOI:——
日期:——
Imide-amide rearrangement under the influence of boron trifluoride etherate
作者:V. A. Gilyarov、B. A. Kvasov、T. M. Shcherbina、M. I. Kabachnik
DOI:10.1007/bf00951895
日期:1980.1
A GC-MS investigation of the mechanism of imide-amide rearrangement
作者:T. M. Shcherbina、A. P. Laretina、V. A. Gilyarov、M. I. Kabachnik
DOI:10.1007/bf00699841
日期:1994.4
The products of imide-amide rearangement of trialkyl (arylimido)phosphates were studied by the GC-MS method. An ionic chain mechanism was suggested for this reaction.