Recent advances in direct asymmetric reaction of furanone

IF 2.1 3区 化学 Q2 CHEMISTRY, ORGANIC
Ling Zhang , Qiang Zhang , Ran Wang , Aiqin Liu , Manfei Liang , Zhushuang Bai
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引用次数: 0

Abstract

Butenoic acid compounds or γ-butyrolactone compounds containing multiple chiral centers widely exist in various natural products and have very important biological activities, such as anti-tumor activity. However, the scarcity of many highly active natural compounds restricts their potential for further research into biological functions and therapeutic applications. Therefore, new methods are required for the efficient synthesis of these compounds. Direct catalytic asymmetric reactions based on furanone have emerged as a promising approach for the quick construction of chiral poly-substituted compounds, enabling the synthesis of biologically active natural products, analogues, and bio-active molecules. In this review, we will explore recent developments in direct catalytic asymmetric reactions based on furanone and their applications in the synthesis of natural products and bioactive molecules.

Abstract Image

呋喃酮直接不对称反应的最新进展
丁烯酸化合物或含有多个手性中心的γ-丁内酯化合物广泛存在于各种天然产物中,具有非常重要的生物活性,如抗肿瘤活性。然而,许多高活性天然化合物的稀缺性限制了它们在生物功能和治疗应用方面的进一步研究潜力。因此,需要新的方法来高效合成这些化合物。基于呋喃酮的直接催化不对称反应已成为快速构建手性多取代化合物的一种很有前途的方法,它使生物活性天然产物、类似物和生物活性分子的合成成为可能。在本综述中,我们将探讨基于呋喃酮的直接催化不对称反应的最新发展及其在天然产物和生物活性分子合成中的应用。
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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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