Oxidative ring opening of 3-hydroxyquinoline-2,4(1H,3H)-diones into N-(α-ketoacyl)anthranilic acids

被引：21

作者：

Kafka, Stanislav ^{[1
]}

Proisl, Karel ^{[1
]}

Kasparkova, Vera ^{[1
]}

Urankar, Damijana ^{[2
]}

Kimmel, Roman ^{[1
]}

Kosmrlj, Janez ^{[2
]}

机构：

[1] Tomas Bata Univ Zlin, Fac Technol, Dept Chem, Zlin 76272, Czech Republic

[2] Univ Ljubljana, Fac Chem & Chem Technol, Ljubljana 1000, Slovenia

来源：

TETRAHEDRON | 2013年 / 69卷 / 51期

关键词：

N-(alpha-Ketoacyl)anthranilic acid; Quinolinones; Quinolinediones; Paraperiodic acid; Periodate; 3-HYDROXY-1,2,3,4-TETRAHYDROQUINOLINE-2,4-DIONES; CHEMISTRY; REARRANGEMENT; DERIVATIVES; ROUTE;

D O I：

10.1016/j.tet.2013.10.092

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

N-(alpha-Ketoacyl)anthranilic acids were prepared by oxidative ring opening of 3-hydroxyquinoline-2,4(1H,3H)-diones by using paraperiodic acid (H5IO6) or sodium periodate (NaIO4). The optimisation of the reaction conditions is described as well as the utilisation of N-(alpha-ketoacyl)anthranilic acids in the preparation of anthranilic acid hydrochlorides. (C) 2013 Elsevier Ltd. All rights reserved.

引用

页码：10826 / 10835

页数：10

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