67278-71-1Relevant articles and documents
Catalyst-Free and Selective C-N Bond Functionalization: Stereospecific Three-Component Coupling of Amines, Dichloromethane, and >P(O)H Species Affording α-Aminophosphorus Compounds
Zhao, Yalei,Chen, Xiuling,Chen, Tieqiao,Zhou, Yongbo,Yin, Shuang-Feng,Han, Li-Biao
, p. 62 - 69 (2015/09/01)
Catalyst-free and selective C-N bond functionalization has been achieved through three-component coupling of amines, dihalomethane, and >P(O)H species. This reaction takes place stereospecifically with retention of configuration at phosphorus, which can produce various new optically active phosphorus analogues of α-amino acids.
Synthesis of new organophosphorus-substituted mono-and bis(trimethylsilyl) amines with pch2n fragments and their derivatives
Prishchenko, Andrey A.,Livantsov, Mikhail V.,Novikova, Olga P.,Livantsova, Ludmila I.,Petrosyan, Valery S.
experimental part, p. 71 - 77 (2011/04/15)
Convenient procedures for the synthesis of new organophosphorus-substituted monoand bis(trimethylsilyl)amines with PCH2N moiety are proposed, starting from trimethylsilyl esters of organophosphorus acids, as well as 1,3,5-trialkylhexahydro-1,3,
Synthesis of phosphorus-substituted dialkylamides of organophosphorus acids, containing PCH2NP fragments
Prishchenko,Livantsov,Novikova,Livantsova,Koval',Grigor'ev
, p. 1317 - 1320 (2007/10/03)
Reactions of [N-(trimethylsilyl)aminomethyl]phosphonates with organophosphorus acid chlorides was studied, which allowed to develop convenient synthetic approaches to novel phosphorus-substrituted dialkylamides of organophosphorus acids, including a PCH2NP fragment. Certain properties of the resulting compounds are presented. 2004 MAIK "Nauka/Interperiodica".