A recyclable palladium catalysis in cross-coupling reactions between aroyl chlorides and sodium tetraphenylborate

Chan Sik Cho

doi:10.1016/j.catcom.2008.05.013

A recyclable palladium catalysis in cross-coupling reactions between aroyl chlorides and sodium tetraphenylborate

Chan Sik Cho

Department of Applied Chemistry

Research output: Contribution to journal › Article › peer-review

8 Scopus citations

Abstract

Aroyl chlorides react with sodium tetraphenylborate in THF at room temperature in the presence of a nano-palladium catalyst prepared from Pd(OAc)₂ and PEG-2000 to give the corresponding diaryl ketones in high yields. The catalytic system could be recovered and reused five times without any loss of catalytic activity.

Original language	English
Pages (from-to)	2261-2263
Number of pages	3
Journal	Catalysis Communications
Volume	9
Issue number	13
DOIs	https://doi.org/10.1016/j.catcom.2008.05.013
State	Published - 20 Jul 2008

Keywords

Aroyl chlorides
Cross-coupling
Ketones
Recyclable palladium catalyst
Sodium tetraphenylborate

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10.1016/j.catcom.2008.05.013

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title = "A recyclable palladium catalysis in cross-coupling reactions between aroyl chlorides and sodium tetraphenylborate",

abstract = "Aroyl chlorides react with sodium tetraphenylborate in THF at room temperature in the presence of a nano-palladium catalyst prepared from Pd(OAc)2 and PEG-2000 to give the corresponding diaryl ketones in high yields. The catalytic system could be recovered and reused five times without any loss of catalytic activity.",

keywords = "Aroyl chlorides, Cross-coupling, Ketones, Recyclable palladium catalyst, Sodium tetraphenylborate",

author = "Cho, {Chan Sik}",

year = "2008",

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AU - Cho, Chan Sik

PY - 2008/7/20

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N2 - Aroyl chlorides react with sodium tetraphenylborate in THF at room temperature in the presence of a nano-palladium catalyst prepared from Pd(OAc)2 and PEG-2000 to give the corresponding diaryl ketones in high yields. The catalytic system could be recovered and reused five times without any loss of catalytic activity.

AB - Aroyl chlorides react with sodium tetraphenylborate in THF at room temperature in the presence of a nano-palladium catalyst prepared from Pd(OAc)2 and PEG-2000 to give the corresponding diaryl ketones in high yields. The catalytic system could be recovered and reused five times without any loss of catalytic activity.

KW - Aroyl chlorides

KW - Cross-coupling

KW - Ketones

KW - Recyclable palladium catalyst

KW - Sodium tetraphenylborate

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DO - 10.1016/j.catcom.2008.05.013

M3 - Article

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SN - 1566-7367

VL - 9

SP - 2261

EP - 2263

JO - Catalysis Communications

JF - Catalysis Communications

IS - 13

ER -

A recyclable palladium catalysis in cross-coupling reactions between aroyl chlorides and sodium tetraphenylborate

Abstract

Keywords

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