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![(2R,2′R-(+)-[N,N′-双（2-吡啶基甲基）]-2,2′-联吡咯烷双（乙腈）六氟锑酸铁（II）](/deepweb/assets/sigmaaldrich/product/structures/202/913/41951272-e38c-4f7b-9bf9-6ed9448f4864/640/41951272-e38c-4f7b-9bf9-6ed9448f4864.png)
方案
≥95%
表单
powder or crystals
反应适用性
core: palladium
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
mp
>300 °C
储存温度
2-8°C
SMILES字符串
N#CC.C1(C2=CC=CC=N2)=CC=CC(C3=NC=CC=C3)=N1.[Pd]
InChI
1S/C15H11N3.C2H3N.Pd/c1-3-10-16-12(6-1)14-8-5-9-15(18-14)13-7-2-4-11-17-13;1-2-3;/h1-11H;1H3;
InChI key
UESWWXSSNHGEKT-UHFFFAOYSA-N
相关类别
应用
[Pd(terpy)(MeCN)][BF4]2 is a versatile palladium precatalyst.
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相关产品
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
Anthony R Mazzotti et al.
Journal of the American Chemical Society, 135(38), 14012-14015 (2013-09-18)
A practical, palladium-catalyzed synthesis of aryl fluorides from arylboronic acid derivatives is presented. The reaction is operationally simple and amenable to multigram-scale synthesis. Evaluation of the reaction mechanism suggests a single-electron-transfer pathway, involving a Pd(III) intermediate that has been isolated
Kumiko Yamamoto et al.
Nature, 554(7693), 511-514 (2018-02-23)
Aryl fluorides are widely used in the pharmaceutical and agrochemical industries, and recent advances have enabled their synthesis through the conversion of various functional groups. However, there is a lack of general methods for direct aromatic carbon-hydrogen (C-H) fluorination. Conventional
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