59758-27-9Relevant articles and documents
Effect of isopropyl group on phosphorylation of phenols with phosphorous amides
Nifant'ev,Suvorkin,Rasadkina,Selyutina,Shishin
, p. 1183 - 1185 (2002)
Reaction of resorcinol with phosphorous triamides containing various aliphatic radicals was studied. The preferential cleavage from phosphorus of the diisopropylamino group compared with the less bulky dimethylamino group was observed for the first time. It was shown that resorcinol is easily phosphorylated under mild conditions independent of the nature of substituent on nitrogen, but sterically hindered bulky radicals on nitrogen slow down phenolysis not only of the first, but also of the second amido group.
Dismutation of diamidoarylphosphites
Nifantyev, Edward E.,Rasadkina, Elena N.,Slitikov, Pavel V.,Vasyanina, Larisa K.
, p. 2465 - 2477 (2007/10/03)
Some examples of spontaneous dismutation of diamidoarylphosphites in different solvents were studied, and features of the process were revealed.
Synthesis and reactions of the novel diphosphine, iPrN=C2
Hund, Heike,Hund, Rolf-Dieter,Has, Senay,Roeschenthaler, Gerd-Volker
, p. 193 (2007/10/03)
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