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Merck
CN

ALD00629

Sigma-Aldrich

6-(1-Cyclohexyl-1-(5-methylpyridin-2-yl)ethyl)pyridin-2(1H)-one

≥95%

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About This Item

经验公式(希尔记法):
C19H24N2O
分子量:
296.41
MDL编号:
UNSPSC代码:
12352100
NACRES:
NA.21

质量水平

方案

≥95%

表单

powder or chunks

mp

146-149 °C

储存温度

−20°C

SMILES字符串

O=C1C=CC=C(N1)C(C2=NC=C(C=C2)C)(C)C3CCCCC3

应用

This ligand was developed by the Yu lab to enable the Pd-catalyzed dehydrogenation of aliphatic carboxylic acids through a typically challenging activation of the β-methylene C-H bond. This method is chemoselective to carboxylic acids even in the presence of other enolizable functional groups, and may also viably utilize molecular oxygen as the terminal oxidant for the transformation.

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

法规信息

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Zhen Wang et al.
Science (New York, N.Y.), 374(6572), 1281-1285 (2021-11-12)
Dehydrogenative transformations of alkyl chains to alkenes through methylene carbon-hydrogen (C–H) activation remain a substantial challenge. We report two classes of pyridine-pyridone ligands that enable divergent dehydrogenation reactions through palladium-catalyzed β-methylene C–H activation of carboxylic acids, leading to the direct
Zhen Li et al.
Science (New York, N.Y.), 372(6549), 1452-1457 (2021-11-30)
Hydroxylation of aryl carbon-hydrogen bonds with transition metal catalysts has proven challenging when oxygen is used as the oxidant. Here, we report a palladium complex bearing a bidentate pyridine/pyridone ligand that efficiently catalyzes this reaction at ring positions adjacent to

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