首页> 外文期刊>Current organic chemistry >Mucochloric and Mucobromic Acids:Inexpensive,Highly Functionalised Starting Materials for the Selective Synthesis of Variously Substituted 2(5H)-Furanone Derivatives,Sulfur- or Nitrogen-Containing Heterocycles and Stereodefined Acyclic Unsaturated Di
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Mucochloric and Mucobromic Acids:Inexpensive,Highly Functionalised Starting Materials for the Selective Synthesis of Variously Substituted 2(5H)-Furanone Derivatives,Sulfur- or Nitrogen-Containing Heterocycles and Stereodefined Acyclic Unsaturated Di

机译:粘氯酸和粘溴酸:廉价,高官能度的原料,用于选择性合成各种取代的2(5H)-呋喃酮衍生物,含硫或氮的杂环和立体定义的非环状不饱和二硫

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2(5H)-Furanonc derivatives are a large family of heterocycles that include synthetically useful compounds,several natural products and drugs with diverse biological activities.From the 1960.there has been a continuous interest in the development of efficient methods for preparation of these heterocycles and in their synthetic applications.The studies in these fields have been summarised and discussed in several excellent reviews,some of which have been recently published.The present article aims at completing the picture of these studies and highlights the most recent results from our and other and our laboratories which have been considered only shortly in previous reviews or have not been reviewed at all.In particular,it deals with the preparation and reactivity of 3.4-dichloro-5-hydroxy-2(5H)-furanone(also called mucochloric acid)and 3,4-dibromo-5-hydroxy-2(5H)-furanone(also called mucobromic acid)and the synthetic applications of these inexpensive,highly functionalised synthons.These applications illustrate that these mucohalic acids can provide a simple and convenient entry to a wide variety of interesting organic compounds and are mainly concerned with the selective and efficient preparation of variously substituted 2(5//)-furanone derivatives,including natural and unnatural compounds,which exhibit anti-inflammatory activity or are characterised by potent cytotoxic activities against human cancer cell lines.Nevertheless,our attempt to tell the"whole story"of mucochloric and mucobromic acids from 1873 up to the present day is also concerned with a discussion on the use of these substances for preparation of Stereodefined acyclic unsaturated dihalogenated derivatives and sulfur- or nitrogen-containing heterocycles,including members,which are precursors to agrochemically important substances.
机译:2(5H)-Furanonc衍生物是一大类杂环,包括合成有用的化合物,几种天然产物和具有多种生物活性的药物。从1960年开始,人们一直在关注开发制备这些杂环的有效方法的兴趣这些领域的研究已在一些出色的评论中进行了总结和讨论,其中一些评论最近已经发表。本文旨在完善这些研究的图片,并重点介绍我们和其他机构的最新成果以及我们之前在不久的评论中仅被考虑或根本没有经过审查的实验室。特别是它涉及3.4-二氯-5-羟基-2(5H)-呋喃酮(也称为粘氯酸)的制备和反应性)和3,4-二溴-5-羟基-2(5H)-呋喃酮(也称为粘溴酸)的合成以及这些廉价,高度官能化的合成子的合成应用。本身的应用表明,这些粘膜卤酸可以为各种有趣的有机化合物提供简便的输入途径,并且主要涉及选择性和有效地制备各种取代的2(5 //)-呋喃酮衍生物,包括天然和非天然化合物然而,我们试图讲述从1873年到今天的粘膜氯酸和粘膜溴酸的“全貌”的尝试,也涉及到有关抗癌活性的研究。这些物质在制备立体定义的无环不饱和二卤代衍生物以及含硫或氮的杂环(包括成员)中的用途,这些成员是农业化学重要物质的前体。

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