936197

AdQPhos Pd G3

• Synonyme(s) : AdQPhos G3 Palladacycle, AdQPhos Palladacycle
• Formule empirique (notation de Hill): C₇₃H₇₂FeNO₃PPdS
• Poids moléculaire : 1236.66
• Code UNSPSC : 12352142
• Nomenclature NACRES : NA.22

Propriétés

• Pureté: ≥90%
• Niveau de qualité: 100
• Forme: powder
• Capacité de réaction: reaction type: Cross Couplings
• Groupe fonctionnel: (palladium); phosphine
• Chaîne SMILES: CS(O[Pd]1([P](C23C[C@H]4C[C@H](C[C@H](C4)C3)C2)(C56C[C@H]7C[C@H](C[C@H](C7)C6)C5)c8cccc8)[NH2]C(C=CC=C9)=C9C%10=C1C=CC=C%10)(=O)=O.c%11(C%12=CC=CC=C%12)c(C%13=CC=CC=C%13)c(C%14=CC=CC=C%14)c(C%15=CC=CC=C%15)c%11C%16=CC=CC=C%16.[Fe]

Description

Description générale

The precatalysts derived from AdQPhos exhibit excellent activity towards palladium-catalyzed α-arylation reactions under milder conditions. The strength of these catalytic systems in enabling such reactions were demonstrated with the broad scope of nucleophiles, including nitroalkanes, nitriles, amides, esters, and ketones. Compared to other state-of-the-art catalysts, this system was far superior and served as the first versatile catalytic system to accommodate all these nucleophiles in this context.

Further, by merging with micellar catalysis, this catalytic system demonstrated the feasibility of enabling α-arylation reactions under mild aqueous conditions. This approach provides an environmentally benign alternative to toxic/hazardous solvents like 1,4-dioxane or NMP, bringing modern organic synthesis closer to being ideally sustainable.

Application

In addition to facilitating α-arylations, these catalysts demonstrate compatibility with various challenging cross-coupling reactions, such as Suzuki-Miyaura, Buchwald-Hartwig aminations, and C-O and C-S cross-couplings.

Informations sur la sécurité

• Code de la classe de stockage: 11 - Combustible Solids
• Classe de danger pour l'eau (WGK): WGK 3
• Point d'éclair (°F): Not applicable
• Point d'éclair (°C): Not applicable