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
收藏
页码：732 / 736
页数：5
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