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

被引：6

作者：

Thiemann, Thies ^{[5
]}

Tanaka, Yasuko ^{[1
]}

Iniesta, Jesus ^{[2
]}

Varghese, H. Tresa ^{[3
]}

Pannicker, C. Yohannan ^{[4
]}

机构：

[1] Kyushu Univ, Inst Mat Chem & Engn, Kasuga, Fukuoka 8168580, Japan

[2] Univ Alicante, Dept Phys Chem, E-03080 Alicante, Spain

[3] Fatima Mata Natl Coll, Dept Phys, Kollam 1, India

[4] TKM Coll Arts & Sci, Dept Phys, Kollam 5, Kerala, India

[5] Kyushu Univ, Interdisciplinary Grad Sch Engn Sci, Kasuga, Fukuoka 8168580, Japan

来源：

JOURNAL OF CHEMICAL RESEARCH | 2009年 / 12期

关键词：

chloroarenes; anthraquinones; Suzuki-Miyaura cross-coupling; tetrakis(triphenylphosphino)palladium; DIELS-ALDER REACTIONS; ARYL CHLORIDES; CATALYSTS; COMPLEXES; CYCLOADDITION; PRECURSORS; OXIDES;

D O I：

10.3184/030823409X12586584303880

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

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

引用

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页码：732 / 736

页数：5

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