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Merck
CN

900534

Sigma-Aldrich

(t-Bu)PhCPhos Pd G3

≥95%

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About This Item

经验公式(希尔记法):
C39H46N3O3PPdS
分子量:
774.26
MDL编号:
UNSPSC代码:
12161600
NACRES:
NA.22

质量水平

方案

≥95%

表单

powder

特点

generation 3

反应适用性

reaction type: Buchwald-Hartwig Cross Coupling Reaction
reaction type: Heck Reaction
reaction type: Hiyama Coupling
reaction type: Negishi Coupling
reaction type: Sonogashira Coupling
reaction type: Stille Coupling
reaction type: Suzuki-Miyaura Coupling
reagent type: catalyst
reaction type: Cross Couplings

官能团

phosphine

SMILES字符串

[Pd+2]c4c(cccc4)c5c(cccc5)[N-H].P(C(C)(C)C)(c2c(cccc2)c3c(cccc3N(C)C)N(C)C)c1ccccc1.[S](=O)(=O)([O-])C

InChI

1S/C26H33N2P.C12H9N.CH4O3S.Pd/c1-26(2,3)29(20-14-9-8-10-15-20)24-19-12-11-16-21(24)25-22(27(4)5)17-13-18-23(25)28(6)7;13-12-9-5-4-8-11(12)10-6-2-1-3-7-10;1-5(2,3)4;/h8-19H,1-7H3;1-6,8-9,13H;1H3,(H,2,3,4);/q;-1;;+2/p-1

InChI key

IYOQFXCZIJAOED-UHFFFAOYSA-M

应用

作为Pd G3络合物,来自Buchwald小组的这种配体催化剂在空间受阻的伯胺的芳基化反应中提供了同类产品中最佳的反应活性。

相关产品

产品编号
说明
价格

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable


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Paula Ruiz-Castillo et al.
Journal of the American Chemical Society, 137(8), 3085-3092 (2015-02-05)
We report the Pd-catalyzed arylation of very hindered α,α,α-trisubstituted primary amines. Kinetics-based mechanistic analysis and rational design have led to the development of two biarylphosphine ligands that allow the transformation to proceed with excellent efficiency. The process was effective in

商品

G3和G4 Buchwald预催化剂是一类最新的空气、湿度和热稳定型交叉偶联复合物,可用于键形成以实现其多功能性和高反应性。

G3 and G4 Buchwald palladium precatalysts are the newest air, moisture, and thermally stable crossing-coupling complexes used in bond formation for their versatility and high reactivity.

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