Synthesis of isatoic anhydride derivatives (microreview)

被引：10

作者：

Bogdanov, Andrei V. ^{[1
]}

Mironov, Vladimir F. ^{[1
]}

机构：

[1] Russian Acad Sci, Kazan Sci Ctr, AE Arbuzov Organ & Phys Chem Inst, 8 Arbuzova St, Kazan 420088, Russia

来源：

CHEMISTRY OF HETEROCYCLIC COMPOUNDS | 2016年 / 52卷 / 02期

基金：

俄罗斯科学基金会;

关键词：

INDOXYL GLYCOSIDES; INHIBITORS; RECEPTOR; CARBONYLATION; EVODIAMINE; CHEMISTRY; OXIDATION; CLEAVAGE; POTENT; SERIES;

D O I：

10.1007/s10593-016-1837-3

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Isatoic anhydride (1H-benzo[d][1,3] oxazine-2,4-dione) and its derivatives are convenient building blocks for the synthesis of various nitrogen-containing heterocyclic structures, such as quinazolines, quinazolones, quinazolinediones, benzodiazepines, quinolinones, and tryptanthrin derivatives. (1) The following methods have been applied to the construction of benzo[d]-[ 1,3] oxazine-2,4-dione ring: cyclization of anthranilic acids, catalytic carbonylation of substituted anilines, transformation of phthalic anhydride derivatives, oxidation of isatin derivatives, and oxidation of indoles with Oxone. This microreview covers data from the last 10 years regarding the synthesis of 1H-benzo[d][1,3] oxazine-2,4-dione derivatives without considering the preparation of its heteroaromatic analogs.

引用

页码：90 / 92

页数：3

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