16433-97-9Relevant academic research and scientific papers
Homolytic substitution at phosphorus for the synthesis of alkyl and aryl phosphanes
Vaillard, Santiago E.,Mueck-Lichtenfeld, Christian,Grimme, Stefan,Studer, Armido
, p. 6533 - 6536 (2008/09/17)
(Chemical Equation Presented) A transition-metal-free radical phosphonation using Me3SnPPh2 and the less toxic Me 3SiPPh2 is reported. These readily available reagents react highly efficiently with primary and secondary alkyl radicals. Moreover, aryl radicals and tertiary alkyl radicals are phosphonated with Me 3SnPPh2 (see scheme; R = aryl, alkyl, vinyl; X = 1, Br, OC(S)imidazolyl). DFT calculations provide insights into the mechanism of the reaction.
Alkenylzirconocene-mediated preparation of alkenylphosphines
Miyaji, Taichi,Xi, Zhenfeng,Ogasawara, Masamichi,Nakajima, Kiyohiko,Takahashi, Tamotsu
, p. 8737 - 8740 (2008/03/13)
(Chemical Equation Presented) Alkenylphosphines with various substituents were prepared by the reaction of an alkenylzirconocene with a chlorophosphine. Reactions of (α-unsubstituted alkenyl)zirconocenes with Ph2PCl or PhPCl2 gave th
ENEPHOSPHINILATION
Mislankar, Dattatraya G.,Mugrage, Ben,Darling, S. D.
, p. 4619 - 4622 (2007/10/02)
A general method is described for the formation of vinylphosphines from arylsulfonylhydrazones.Oxidation of the resulting vinylphosphines yields phosphine oxides.
