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通过胡桃醌衍生物环化反应合成呋喃萘醌及其生物学特性的综述。

A review on synthesis of furonaphthoquinones through lawsone derivatives annulation reactions and their biological properties.

作者信息

Olyaei Abolfazl, Sadeghpour Mahdieh, Sajjadi Seyede Bita

机构信息

Department of Chemistry, Faculty of Science, Imam Khomeini International University Qazvin Iran.

Department of Chemistry, Qazvin Branch, Islamic Azad University Qazvin Iran

出版信息

RSC Adv. 2025 Feb 4;15(5):3515-3546. doi: 10.1039/d4ra08843c. eCollection 2025 Jan 29.

Abstract

Furonaphthoquinones and their dihydro derivatives have attracted significant attention due to their diverse pharmacological activities. These compounds can be derived from natural sources, including various plants, or synthesized through chemical methods, resulting in a wide variety of structures with distinct biological properties. As a result, numerous methods have been developed over the past decades for the preparation of these compounds, particularly utilizing 2-hydroxy-1,4-naphthoquinone derivatives as key precursors. Considering these concepts, this review aims to offer a comprehensive overview of the chemical synthesis of linear and angular furonaphthoquinones, along with their dihydro derivatives derived from 2-hydroxy-1,4-naphthoquinones annulation reactions, and to explore their diverse biological activities.

摘要

呋喃萘醌及其二氢衍生物因其多样的药理活性而备受关注。这些化合物可来源于包括各种植物在内的天然来源,或通过化学方法合成,从而产生具有不同生物学特性的多种结构。因此,在过去几十年中已经开发出许多制备这些化合物的方法,特别是利用2-羟基-1,4-萘醌衍生物作为关键前体。考虑到这些概念,本综述旨在全面概述线性和角型呋喃萘醌及其由2-羟基-1,4-萘醌环化反应衍生的二氢衍生物的化学合成,并探索它们多样的生物活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65a6/11793157/1f51065fbffa/d4ra08843c-f1.jpg

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