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基于2-叠氮苯甲醛的[4+2]环化反应合成喹啉衍生物

2-Azidobenzaldehyde-Based [4+2] Annulation for the Synthesis of Quinoline Derivatives.

作者信息

Zhang Xiaofeng, Liu Miao, Qiu Weiqi, Zhang Wei

机构信息

Center for Green Chemistry and Department of Chemistry, University of Massachusetts Boston, 100 Morrissey Blvd, Boston, MA 02125, USA.

Department of Medicinal Chemistry, Cerevel Therapeutics, Cambridge, MA 02141, USA.

出版信息

Molecules. 2024 Mar 11;29(6):1241. doi: 10.3390/molecules29061241.

Abstract

Quinoline is a privileged heterocyclic ring which can be found in many drug molecules and bioactive compounds. The development of synthetic methods for making quinoline derivatives continuously attracts the interest of organic and medicinal chemists. This paper highlights 2-azidobenzaldehyde-based [4+2] annulation for the synthesis of quinoline derivatives including fused and spiro-quinolines, quinoline-4-ols, 4-aminoquinolines, and related compounds.

摘要

喹啉是一种具有特殊结构的杂环,存在于许多药物分子和生物活性化合物中。喹啉衍生物合成方法的开发一直吸引着有机化学家和药物化学家的关注。本文重点介绍了基于2-叠氮基苯甲醛的[4+2]环化反应,用于合成喹啉衍生物,包括稠合和螺环喹啉、喹啉-4-醇、4-氨基喹啉及相关化合物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2234/10975811/d843a8ed5b14/molecules-29-01241-g001.jpg

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