202208-62-6Relevant articles and documents
Zwitterionic Phosphoranides as Intermediates in the Reaction of Phosphorus Tribromide with N,N-Dimethyl-N′-arylformamidines
Marchenko, Anatoliy P.,Koidan, Georgyi N.,Hurieva, Anastasia N.,Rozhenko, Alexander B.,Kostyuk, Aleksandr N.
, p. 12 - 22 (2016/02/09)
Cyclic zwitterionic phosphoranides 2a,b were found to be intermediate products in the reaction of N,N-dimethyl-N′-(aryl)formamidines with PBr3. The structure of phosphoranide 2a was determined by means of the X-ray and quantum chemistry investigations. Mechanism of its formation was proposed based on Density functional theory (DFT) calculations. Reactions of 2 with amines and selenium yielded either C-phosphorylated formamidines or benzazaphospholes. The first example of intramolecular heterocyclization of a pentavalent phosphorus derivative 15b into 3Cyrillic capital letter en-1,3-benzazaphosphole has been demonstrated.
Convenient method for the synthesis of C-phosphorylated N-arylformamidines
Marchenko, Anatoliy,Koidan, Georgyi,Hurieva, Anastasiya,Merkulov, Anatoliy,Pinchuk, Aleksandr,Yurchenko, Aleksandr,Kostyuk, Aleksandr
experimental part, p. 3668 - 3677 (2010/07/04)
C-Phosphorylated (PV) arylformamidines have been prepared by the reaction of N-arylamidotrichloromethyl derivatives of phosphorus, thiophosphorus, and selenophosphorus acids with secondary amines. Dependence of the reaction on the nature of cha