中文名：烯丙基氯[1,3-双(2,6-二异丙基苯基)-4,5-二氢咪唑-2-亚甲基]钯(II)
英文名：Allyl[1,3-bis(2,6-diisopropylphenyl)-2-imidazolidinylidene]chloropalladium(II)
纯度：≥99.95% metals basis
货号：A284063
Cas号：478980-01-7
存储温度：2-8°C储存,充氩
运输条件：低温运输
产品介绍：
Product class
M-P, Homogeneous Catalysts, N-Heterocyclic Carbene Ligands, M-C, Allyl Ligands, SIPr, Bidentate Ligands
Reaction type
Cross Coupling Reactions with Arenes, Amination, Buchwald-Hartwig Aminaton, Alpha Arylation, Suzuki-Miyaura Coupling Reaction
Chemical properties
Theoretical metal content
Applications & references
α-Arylation of ketones.
Reference: Org. Lett. 2002, 4, 4053 (DOI: 10.1021/ol026745m); Adv. Synth. Catal. 2012, 354, 377 (DOI: 10.1002/adsc.201100669)
Intramolecular arylamination step in the synthetic approach of cryptocarya alkaloids.
Reference: Synlett 2003, 12, 1871 (DOI: 10.1021/jo035834p)
Suzuki-Miyaura coupling reaction.
Reference: J. Org. Chem. 2004, 69, 3173
Buchwald-Hartwig coupling reactions.
Reference: J. Am. Chem. Soc. 2006, 128, 4101 (DOI: 10.1021/ja057704z)
α-Heteroarylation of ketone enolates.
Reference: J. Org. Chem. 2010, 75, 5316 (DOI: 10.1021/jo100623d)
Palladium catalyzed anaerobic oxidation of secondary alcohols under mild reaction conditions.
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)
查看阿拉丁官网此产品相关对应页面：https://www.aladdin-e.com/zh_cn/A284063.html
关键字： Umicore CX23;(SIPr)Pd(allyl)Cl, Allyl[1,3-bis(2,6-diisopropylphenyl)-2-imidazolidinylidene]chloropalladium(II), Allylchloro-[1,3-bis-(2,6-diisopropylphenyl)-2-imidazolidinylidene]palladium(II), Allylchloro[1,3-bis-(2,6-diisopropylphenyl)imidazol-2-idinyli;Umicore CX23;(SIPr)Pd(allyl)Cl, Allyl[1,3-bis(2,6-diisopropylphenyl)-2-imidazolidinylidene]chloropalladium(II), Allylchloro-[1,3-bis-(2,6-diisopropylphenyl)-2-imidazolidinylidene]palladium(II), Allylchloro[1,3-bis-(2,6-diisopropylphenyl)imidazol-2-idinyli
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