723-45-5Relevant academic research and scientific papers
Nickel-catalyzed coupling of R2P(O)Me (R = aryl or alkoxy) with (hetero)arylmethyl alcohols
Li, Wei-Ze,Wang, Zhong-Xia
, p. 2233 - 2242 (2021/03/24)
α-Alkylation of methyldiarylphosphine oxides with (hetero)arylmethyl alcohols was performed under nickel catalysis. Various arylmethyl and heteroarylmethyl alcohols can be used in this transformation. A series of methyldiarylphosphine oxides were alkylated with 30-90% yields. Functional groups on the aromatic rings of methyldiarylphosphine oxides or arylmethyl alcohols including OMe, NMe2, SMe, CF3, Cl, and F groups can be tolerated. The conditions are also suitable for the α-alkylation reaction of dialkyl methylphosphonates.
A new palladium-catalyzed P-C coupling reaction: Synthesis of triarylphosphine oxides and diarylmethylphosphine oxides
Stark, Gene A.,Riermeier, Thomas H.,Beller, Matthias
, p. 1703 - 1711 (2007/10/03)
The first palladium-catalyzed P-C coupling reaction of aryl halides with (hydroxymethyl)phosphines is described. Hydroxymethylphosphines act as cheap and easy to use H3PO and CH3P(O)H2 equivalents. Tertiary diarylmethylphosphine oxides 5 and triarylphosphine oxides 6 are accessible in a one pot reaction in overall yields between 45-60%.
