Ruthenium-catalysed oxidative cyclisation of 2-aminobenzyl alcohol with ketones: modified Friedlaender quinoline synthesis

被引：233

作者：

Cho, CS ^{[1
]}

Kim, BT

Kim, TJ

Shim, SC

机构：

[1] Kyungpook Natl Univ, Coll Engn, Dept Ind Chem, Taegu 702701, South Korea

[2] Kyungpook Natl Univ, Ind Technol Res Inst, Taegu 702701, South Korea

来源：

CHEMICAL COMMUNICATIONS | 2001年 / 24期

关键词：

D O I：

10.1039/b109245f

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

2-Aminobenzyl alcohol is oxidatively cyclised with an array of ketones in dioxane at 80 degreesC in the presence of a catalytic amount of a ruthenium catalyst and KOH to afford the corresponding quinolines in high yields.

引用

页码：2576 / 2577

页数：2

共 19 条

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[2] CHENG CC, 1982, ORG REACTIONS, V28, P37
[3] Synthesis of quinolines via ruthenium-catalysed amine exchange reaction between anilines and trialkylamines
Cho, CS
Oh, BH
Kim, JS
Kim, TJ
Shim, SC
[J]. CHEMICAL COMMUNICATIONS, 2000, (19) : 1885 - 1886
[4] Ruthenium-catalyzed heteroannulation of anilines with alkanolammonium chlorides leading to indoles
Cho, CS
Kim, JH
Kim, TJ
Shim, SC
[J]. TETRAHEDRON, 2001, 57 (16) : 3321 - 3329
[5] Cho CS, 2001, B KOR CHEM SOC, V22, P545
[6] Ruthenium-catalysed synthesis of indoles from anilines and trialkanolamines in the presence of tin(II) chloride dihydrate
Cho, CS
Lim, HK
Shim, SC
Kim, TJ
Choi, HJ
[J]. CHEMICAL COMMUNICATIONS, 1998, (09) : 995 - 996
[7] Ruthenium-catalyzed synthesis of indoles from anilines and trialkanolammonium chlorides in an aqueous medium
Cho, CS
Kim, JH
Shim, SC
[J]. TETRAHEDRON LETTERS, 2000, 41 (11) : 1811 - 1814
[8] Synthesis of quinolines by ruthenium-catalyzed heteroannulation of anilines with 3-amino-1-propanol
Cho, CS
Oh, BH
Shim, SC
[J]. JOURNAL OF HETEROCYCLIC CHEMISTRY, 1999, 36 (05) : 1175 - 1178
[9] Ruthenium-catalyzed synthesis of quinolines from anilines and allylammonium chlorides in an aqueous medium via amine exchange reaction
Cho, CS
Kim, JS
Oh, BH
Kim, TJ
Shim, SC
Yoon, NS
[J]. TETRAHEDRON, 2000, 56 (39) : 7747 - 7750
[10] Cho CS, 2001, ANGEW CHEM INT EDIT, V40, P958, DOI 10.1002/1521-3773(20010302)40:5<958::AID-ANIE958>3.0.CO

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