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通过弗里德兰德缩合和卡多根环化合成 11H-吲哚并[3,2-c]喹啉框架的简便方法

IF 0.8 4区 化学 Q4 CHEMISTRY, ORGANIC
Arkivoc Pub Date : 2024-06-11 DOI:10.24820/ark.5550190.p012.176
Sheng Liu, Ru Li
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引用次数: 0

摘要

通过弗里德兰德缩合和卡多根环化两个步骤，从邻氨基苯甲醛和 2-硝基苯基取代酮制备出了带有各种取代基的吲哚并[3,2-c]喹啉。
本文章由计算机程序翻译，如有差异，请以英文原文为准。
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A convenient synthetic approach to 11H-indolo[3,2-c]quinoline framework via Friedlander condensation and Cadogan cyclization
Indolo[3,2-c ]quinolines bearing various substituents have been prepared from o-aminobenzaldehydes and 2-nitrophenyl substituted ketones through a two-step sequence involving Friedlander condensation and Cadogan cyclization.
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来源期刊
Arkivoc
Arkivoc 化学-有机化学
CiteScore
1.10
自引率
11.10%
发文量
120
审稿时长
3.1 months
期刊介绍： Arkivoc publishes full papers (not accounts) describing sound original work that is of interest to organic chemists (in areas of synthetic organic chemistry, bio-organic, organometallic, theoretical, and physical organic chemistry: General Papers describing sound original work Reviews and Accounts of selected topics Honorary Issues - Pay tribute to distinguished organic chemists (invited contributions) Thematic Issues - Cover important current topics in organic chemistry Regional Issues - Recognize organic chemistry in various countries.
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