175407-89-3Relevant articles and documents
Copper(I) complexes with remotely functionalized phosphine ligands: Synthesis, structural variety, photophysics and effect onto the optical properties
Achard, Thierry,Bellemin-Laponnaz, Stéphane,Bissessar, Damien,Egly, Julien,Heinrich, Beno?t,Mauro, Matteo,Steffanut, Pascal
, (2021)
The synthesis, chemical and photophysical investigation of a series of eight novel copper-halide derivatives with different nuclearity is herein presented. One mononuclear copper(I) complex with formula [CuI(pyridine)(P)2], where P is a functio
Catalyst-free hydrophosphination of alkenes in presence of 2-methyltetrahydrofuran: A green and easy access to a wide range of tertiary phosphines
Bissessar, Damien,Egly, Julien,Achard, Thierry,Steffanut, Pascal,Bellemin-Laponnaz, Stéphane
, p. 27250 - 27256 (2019/09/12)
A hydrophosphination reaction that is free of base, acid and catalyst, using only 2-methyltetrahydrofuran as additive has been performed. A new family of mono-, di-, tri- and tetra-phosphines compounds are obtained in good to excellent yields by adding di
Chemically-tagged Mitsunobu reagents for use in solution-phase chemical library synthesis
Starkey, Gale W.,Parlow, John J.,Flynn, Daniel L.
, p. 2385 - 2390 (2007/10/03)
A general method for high-throughput product purification of Mitsunobu reactions is described. Tagged phosphine and azodicarboxylate reagents are used to synthesize individual library members in solution-phase. Workup and purification are easily accomplished by post-reaction sequestration of the tagged reagents and reagent byproducts by a complementary functionalized ion exchange resin. The reagents are utilized in a 3 step library synthesis.