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基于范吕森噁唑合成法的噁唑类分子合成的最新进展。

Recent Advances in the Synthesis of Oxazole-Based Molecules via van Leusen Oxazole Synthesis.

机构信息

College of Chemistry, Jilin University, Changchun 130012, China.

College of Plant Science, Jilin University, Changchun 130062, China.

出版信息

Molecules. 2020 Mar 31;25(7):1594. doi: 10.3390/molecules25071594.


DOI:10.3390/molecules25071594
PMID:32244317
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7180750/
Abstract

Oxazole compounds, including one nitrogen atom and one oxygen atom in a five-membered heterocyclic ring, are present in various biological activities. Due to binding with a widespread spectrum of receptors and enzymes easily in biological systems through various non-covalent interactions, oxazole-based molecules are becoming a kind of significant heterocyclic nucleus, which have received attention from researchers globally, leading them to synthesize diverse oxazole derivatives. The van Leusen reaction, based on tosylmethylisocyanides (TosMICs), is one of the most appropriate strategies to prepare oxazole-based medicinal compounds. In this review, we summarize the recent advances of the synthesis of oxazole-containing molecules utilizing the van Leusen oxazole synthesis from 1972, aiming to look for potential oxazole-based medicinal compounds, which are valuable information for drug discovery and synthesis.

摘要

唑类化合物,包括五元杂环中环上的一个氮原子和一个氧原子,具有多种生物活性。由于唑类分子通过各种非共价相互作用容易在生物系统中与广泛的受体和酶结合,因此成为一种重要的杂环核,引起了全球研究人员的关注,促使他们合成了多种唑类衍生物。基于对甲苯磺酰甲基异氰化物(TosMICs)的范吕森反应(van Leusen reaction)是制备基于唑的药物化合物的最适宜策略之一。在这篇综述中,我们总结了自 1972 年以来利用范吕森唑合成法合成含唑分子的最新进展,旨在寻找有潜力的基于唑的药物化合物,为药物发现和合成提供有价值的信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b702/7180750/65bad9d4d254/molecules-25-01594-sch008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b702/7180750/39da6c5a584e/molecules-25-01594-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b702/7180750/accbcc876dd3/molecules-25-01594-sch002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b702/7180750/76e114c5dc01/molecules-25-01594-sch003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b702/7180750/997be25daa42/molecules-25-01594-sch004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b702/7180750/f2dec9ea51f0/molecules-25-01594-sch005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b702/7180750/c8399f85b311/molecules-25-01594-sch006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b702/7180750/e6ea7a456127/molecules-25-01594-sch007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b702/7180750/65bad9d4d254/molecules-25-01594-sch008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b702/7180750/39da6c5a584e/molecules-25-01594-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b702/7180750/accbcc876dd3/molecules-25-01594-sch002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b702/7180750/76e114c5dc01/molecules-25-01594-sch003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b702/7180750/997be25daa42/molecules-25-01594-sch004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b702/7180750/f2dec9ea51f0/molecules-25-01594-sch005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b702/7180750/c8399f85b311/molecules-25-01594-sch006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b702/7180750/e6ea7a456127/molecules-25-01594-sch007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b702/7180750/65bad9d4d254/molecules-25-01594-sch008.jpg

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本文引用的文献

[1]
Synthesis of Imidazole-Based Medicinal Molecules Utilizing the van Leusen Imidazole Synthesis.

Pharmaceuticals (Basel). 2020-3-3

[2]
Design, synthesis and biological evaluation of imidazole and oxazole fragments as HIV-1 integrase-LEDGF/p75 disruptors and inhibitors of microbial pathogens.

Bioorg Med Chem. 2020-1-1

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ACS Omega. 2017-10-2

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BMC Chem. 2019-2-4

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Front Chem. 2019-6-14

[6]
Recent advances and applications of p-toluenesulfonylmethyl isocyanide (TosMIC).

Org Biomol Chem. 2019-7-17

[7]
MCR Scaffolds Get Hotter with F-Labeling.

Molecules. 2019-4-4

[8]
The LANCA three-component reaction to highly substituted β-ketoenamides - versatile intermediates for the synthesis of functionalized pyridine, pyrimidine, oxazole and quinoxaline derivatives.

Beilstein J Org Chem. 2019-3-13

[9]
Oxazole-Based Compounds As Anticancer Agents.

Curr Med Chem. 2019

[10]
Synthesis of Multi-Substituted Pyrrole Derivatives Through [3+2] Cycloaddition with Tosylmethyl Isocyanides (TosMICs) and Electron-Deficient Compounds.

Molecules. 2018-10-17

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