Arylation of chloroanthraquinones by surprisingly facile Suzuki-Miyaura cross-coupling reactions

Thies Thiemann; Yasuko Tanaka; Jesus Iniesta; H. Tresa Varghese; C. Yohannan Pannicker

doi:10.3184/030823409X12586584303880

Arylation of chloroanthraquinones by surprisingly facile Suzuki-Miyaura cross-coupling reactions

Thies Thiemann
, Yasuko Tanaka
, Jesus Iniesta
, H. Tresa Varghese
, C. Yohannan Pannicker

Department of Chemistry

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

6 Citations (Scopus)

Abstract

Chloroanthraquinones were found to undergo facile Suzuki-cross coupling with substituted phenyl boronic acids using a commercial catalyst Pd(PPh ₃)₄ and with Pd(PPh₃)₄ prepared in situ from Pd(PPh₃)₂Cl₂ and PPh₃.

Original language	English
Pages (from-to)	732-736
Number of pages	5
Journal	Journal of Chemical Research
Issue number	12
DOIs	https://doi.org/10.3184/030823409X12586584303880
Publication status	Published - 2009

Keywords

Anthraquinones
Chloroarenes
Suzuki-Miyaura cross-coupling
Tetrakis(triphenylphosphino)palladium

ASJC Scopus subject areas

General Chemistry

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10.3184/030823409X12586584303880

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title = "Arylation of chloroanthraquinones by surprisingly facile Suzuki-Miyaura cross-coupling reactions",

abstract = "Chloroanthraquinones were found to undergo facile Suzuki-cross coupling with substituted phenyl boronic acids using a commercial catalyst Pd(PPh 3)4 and with Pd(PPh3)4 prepared in situ from Pd(PPh3)2Cl2 and PPh3.",

keywords = "Anthraquinones, Chloroarenes, Suzuki-Miyaura cross-coupling, Tetrakis(triphenylphosphino)palladium",

author = "Thies Thiemann and Yasuko Tanaka and Jesus Iniesta and Varghese, \{H. Tresa\} and Pannicker, \{C. Yohannan\}",

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T1 - Arylation of chloroanthraquinones by surprisingly facile Suzuki-Miyaura cross-coupling reactions

AU - Thiemann, Thies

AU - Tanaka, Yasuko

AU - Iniesta, Jesus

AU - Varghese, H. Tresa

AU - Pannicker, C. Yohannan

PY - 2009

Y1 - 2009

N2 - Chloroanthraquinones were found to undergo facile Suzuki-cross coupling with substituted phenyl boronic acids using a commercial catalyst Pd(PPh 3)4 and with Pd(PPh3)4 prepared in situ from Pd(PPh3)2Cl2 and PPh3.

AB - Chloroanthraquinones were found to undergo facile Suzuki-cross coupling with substituted phenyl boronic acids using a commercial catalyst Pd(PPh 3)4 and with Pd(PPh3)4 prepared in situ from Pd(PPh3)2Cl2 and PPh3.

KW - Anthraquinones

KW - Chloroarenes

KW - Suzuki-Miyaura cross-coupling

KW - Tetrakis(triphenylphosphino)palladium

UR - https://www.scopus.com/pages/publications/73949146447

UR - https://www.scopus.com/pages/publications/73949146447#tab=citedBy

U2 - 10.3184/030823409X12586584303880

DO - 10.3184/030823409X12586584303880

M3 - Article

AN - SCOPUS:73949146447

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SP - 732

EP - 736

JO - Journal of Chemical Research

JF - Journal of Chemical Research

IS - 12

ER -

Arylation of chloroanthraquinones by surprisingly facile Suzuki-Miyaura cross-coupling reactions

Abstract

Keywords

ASJC Scopus subject areas

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