7077-62-5Relevant articles and documents
Reactions de tris(alcoxy)iminophosphanes avec l'acetylene dicarboxylate de methyle: ylure, phosphonate et phosphorane
Bellan, Jacques,Sanchez, Michel,Marre-Mazieres, Marie-Rose,Murillo Beltran, Arturo
, p. 491 - 495 (2007/10/02)
The tris(alkoxy) N-phenyl iminophosphanes react under mild conditions with acetylenic carboxylates to give phosphorus ylides with a β carbonyl group.These compounds, well characterized in the reaction mixture, have not been isolated.They are highly reactive and depending on the nature of substituents on phosphorus atom; give phosphonates, phosphoranes and cyclic ylides.
INDUCTIVE AND STERIC EFFECTS IN THE STAUDINGER REACTION
Gololobov, Yu.,Kasukhin, L.,Ponomarchuk, M.,Klepa, T.,Yurchenko, R.
, p. 339 - 342 (2007/10/02)
The sterically unhindered mode of the electrophilic addition of phenyl azide to trivalent phosphorus compounds and the inductive control in this initial step of the Staudinger reaction have been observed and discussed.