Two routes of heterocyclization of 2-alkynylanthraquinone-1-diazonium salts.: The synthesis of 1H-naphtho[2,3-h]cinnoline-4,7,12-trione

被引：15

作者：

Fedenok, LG ^{[1
]}

Barabanov, II ^{[1
]}

Ivanchikova, ID ^{[1
]}

机构：

[1] Russian Acad Sci, Inst Chem Kinet & Combust, Siberian Branch, Novosibirsk 630090, Russia

来源：

TETRAHEDRON | 2001年 / 57卷 / 07期

基金：

俄罗斯基础研究基金会;

关键词：

Richter reaction; ortho-alkynylarenediazonium salts; heterocyclization; 3-substituted naphthoindazolediones and naphthocinnolinetriones;

D O I：

10.1016/S0040-4020(00)01101-7

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

The possibility of the heterocyclization of vic-alkynylanthraquinonediazonium salts with the formation of a 5- or 6-membered ring, depending on the reaction conditions, is established. The heterocyclization of 2-alkynyl-9,10-anthraquinone-1-diazonium salts to form 1H-naphtho[2,3-h]cinnoline-4,7,12-triones is reported. (C) 2001 Elsevier Science Ltd. All rights reserved.

引用

页码：1331 / 1334

页数：4

共 3 条

[1] Towards understanding the Richter reaction. Peculiarities of heterocyclization of 3-diethylamino-6-(heptyn-1-yl)-1,4-naphthoquinone-5-diazonium chloride [J].

Fedenok, LG ;

Barabanov, II ;

Ivanchikova, ID .

TETRAHEDRON LETTERS, 1999, 40 (04) :805-808

[2]

Porter A. E. A, 1979, COMPREHENSIVE ORGANI, V4, P122

[3] AN UNUSUAL DIRECTION OF THE RICHTER SYNTHESIS - 1H-NAPHTHO[2,3-G]INDAZOLE-6,11-DIONES [J].

SHVARTSBERG, MS ;

IVANCHIKOVA, ID ;

FEDENOK, LG .

TETRAHEDRON LETTERS, 1994, 35 (36) :6749-6752

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