Synthesis of pyrrolo[1,2-a]quinoline and pyrrolo[1,2-b]isoquinoline derivatives via intramolecular acylation

IF 2.1 3区 化学 Q2 CHEMISTRY, ORGANIC Tetrahedron Pub Date : 2024-08-30 DOI:10.1016/j.tet.2024.134224
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Abstract

A methanesulfonic acid mediated intramolecular acylation approach for the synthesis of pyrrolo[1,2-a]quinoline and the isomeric pyrrolo[1,2-b]isoquinoline frameworks has been developed. The reaction is carried out at ambient temperature and no Lewis acid catalyst is required. The product yields are generally good to excellent.

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通过分子内酰化合成吡咯并[1,2-a]喹啉和吡咯并[1,2-b]异喹啉衍生物
本研究开发了一种甲磺酸介导的分子内酰化方法,用于合成吡咯并[1,2-a]喹啉和异构吡咯并[1,2-b]异喹啉框架。反应在常温下进行,无需路易斯酸催化剂。产品收率一般都很高,甚至非常高。
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来源期刊
Tetrahedron
Tetrahedron 化学-有机化学
CiteScore
3.90
自引率
4.80%
发文量
439
审稿时长
34 days
期刊介绍: Tetrahedron publishes full accounts of research having outstanding significance in the broad field of organic chemistry and its related disciplines, such as organic materials and bio-organic chemistry. Regular papers in Tetrahedron are expected to represent detailed accounts of an original study having substantially greater scope and details than that found in a communication, as published in Tetrahedron Letters. Tetrahedron also publishes thematic collections of papers as special issues and ''Reports'', commissioned in-depth reviews providing a comprehensive overview of a research area.
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