(s)-(-) -2,2- Bis (diphénylphosphino) -1,1 - binaphtalène, 97 %

Non disponible en dehors du Royaume-Uni et de l'Irlande

Application

Reactant involved in: Enantioselective and diastereoselective unpoled carbonyl allylation Syntehsis of organophophine oxides as anittumor agents SN2 halogenation of hydroxy groups Synthesis of BINAP complexes Studies of conformational flexibility of BINAP chelates

2,2′-Bis(diphenylphosphino)-1,1′-binaphthyl and its rhodium and ruthenium derivatives are highly selective homogeneous catalysts used for the reduction of aryl ketones, β-keto esters, and α-amino ketones. They have also been used for asymmetric hydrogenation and hydroformylation of olefins, asymmetric Heck reactions, and asymmetric isomerizations of allyls.Ligand used in a palladium-catalyzed, asymmetric, tandem Heck reaction-carbanion capture process leading to a synthesis of a tricyclic sesquiterpene. Also used in a ruthenium-catalyzed asymmetric hydrogenation of α,β-unsaturated acids.

Packaging

250 mg in glass insert

1, 5 g in glass bottle