计算溶液所需的质量、体积或浓度。
提供 ≥99.95% metals basis 纯度,适用于对基线干扰要求严格的色谱和分析工作流程。
2-8°C储存,避光,充氩。低温运输 。请查阅批次 COA 获取详细规格。
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在色谱分析、有机合成和交叉偶联反应领域已被 0 篇同行评审文献引用。
Allyl[1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene]chloropalladium(II) is an air-stable, well-defined palladium N-heterocyclic carbene complex, which can efficiently catalyze α-arylation of ketones.
Catalyst for the arylation of ketones, Suzuki coupling reaction, Buchwald-Hartwig amination reaction, dehalogenation of aryl chlorides, and oxidation of secondary alcohols.
Product class
M-P, Homogeneous Catalysts, N-Heterocyclic Carbene Ligands, M-C, Allyl Ligands, IPr, Bidentate Ligands
Reaction type
Cross Coupling Reactions with Arenes, Amination, Buchwald-Hartwig Aminaton, Alpha Arylation, Dehalogenation, Kumada Coupling Reaction, Mizoroki Heck Coupling Reaction, Oxidation, Suzuki-Miyaura Coupling Reaction, Dehalogenation, Oxidation, Telomerization
Chemical properties
C30H41N2ClPd
[(IPr)Pd(allyl)CI]
571.54
Pd
19
crystalline
99.95
Applications & references
Palladium catalyzed anaerobic oxidation of secondary alcohols under mild reaction conditions.
Reference: J. Org. Chem. 2011, 76, 1390. (DOI: 10.1021/jo102385u)
One-pot oxidation / α-ketone arylation of secondary alcohols.
Reference: J. Org. Chem. 2011, 76, 1390. (DOI: 10.1021/jo102385u)
Palladium catalyzed Buchwald-Hartwig-Reaction at room temperature.
Reference: J. Am. Chem. Soc. 2006, 128, 4101. (DOI: 10.10217ja057704z)
α-Arylation of propiophenone.
Reference: Org. Lett. 2002, 4, 4053 (DOI: 10.1021/ol026745m)
Intramolecular arylamination step in the total synthesis of cryptocarya alkaloids.
Reference: Synlett 2003, 12, 1871 (DOI: 10.1055/s-2003-41468)
Dehalogenation reaction.
Reference: J. Org. Chem. 2004, 69, 3173 (DOI: 10.1021/jo035834p)
Suzuki-Miyaura coupling reaction.
Reference: J. Am. Chem. Soc. 2006, 128, 4101. (DOI: 10.10217ja057704z)
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