83438-76-0Relevant academic research and scientific papers
Reactivity patterns of benzhydryl(mesityl)phosphane oxide–a potential intermediate in carbonyl-carbonyl coupling reactions?
D’Imperio, Nicolas,Arkhypchuk, Anna I.
, p. 575 - 579 (2019)
Benzhydryl(mesityl)phosphane oxide 2-H is prepared and its deprotonation and nucleophilicity behavior investigated. Treatment of lithium salts of 2-H with MeI results in methylation at the P-center while the benzyl carbon is not affected. Only upon double lithiation, it is possible to methylate also the benzyl carbon. Di-anion 2-2Li is reactive towards benzaldehyde to afford moderate amounts of triphenylethene after basic work.
A NUCLEOPHILIC REACTION OF A PHOSPHAALKENE: THE METHYLATION OF MESITYLDIPENYLMETHYLENEPHOSPHINE
Knaap, Th. A. van der,Bickelhaupt, F.
, p. 2037 - 2040 (2007/10/02)
The reaction of the title compound (1) with methyl iodide gives the ylide 3 and the phosphonium salt 4.The intermediate formation of the phosphoniaalkene 2 is postulated.
