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Merck

936200

Sigma-Aldrich

AdQPhos Pd G4

别名:

AdQPhos G4 Palladacycle, AdQPhos Palladacycle

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About This Item

经验公式(希尔记法):
C74H74FeNO3PPdS
分子量:
1250.69
分類程式碼代碼:
12352142
NACRES:
NA.21

形狀

powder

品質等級

反應適用性

reaction type: Cross Couplings

顏色

red to purple

官能基

(palladium)
phosphine

SMILES 字串

CS(O[Pd](C1=C(C2=C3C=CC=C2)C=CC=C1)([P](C45C[C@H]6C[C@H](C[C@H](C6)C5)C4)(C78C[C@H]9C[C@H](C[C@H](C9)C8)C7)c%10cccc%10)[NH]3C)(=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]

一般說明

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.

應用

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.

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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