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

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-ba...

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Detalles Bibliográficos
Autores principales: Zheng, Xunan, Liu, Wei, Zhang, Dawei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7180750/
https://www.ncbi.nlm.nih.gov/pubmed/32244317
http://dx.doi.org/10.3390/molecules25071594
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author Zheng, Xunan
Liu, Wei
Zhang, Dawei
author_facet Zheng, Xunan
Liu, Wei
Zhang, Dawei
author_sort Zheng, Xunan
collection PubMed
description 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.
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spelling pubmed-71807502020-05-01 Recent Advances in the Synthesis of Oxazole-Based Molecules via van Leusen Oxazole Synthesis Zheng, Xunan Liu, Wei Zhang, Dawei Molecules Review 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. MDPI 2020-03-31 /pmc/articles/PMC7180750/ /pubmed/32244317 http://dx.doi.org/10.3390/molecules25071594 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Zheng, Xunan
Liu, Wei
Zhang, Dawei
Recent Advances in the Synthesis of Oxazole-Based Molecules via van Leusen Oxazole Synthesis
title Recent Advances in the Synthesis of Oxazole-Based Molecules via van Leusen Oxazole Synthesis
title_full Recent Advances in the Synthesis of Oxazole-Based Molecules via van Leusen Oxazole Synthesis
title_fullStr Recent Advances in the Synthesis of Oxazole-Based Molecules via van Leusen Oxazole Synthesis
title_full_unstemmed Recent Advances in the Synthesis of Oxazole-Based Molecules via van Leusen Oxazole Synthesis
title_short Recent Advances in the Synthesis of Oxazole-Based Molecules via van Leusen Oxazole Synthesis
title_sort recent advances in the synthesis of oxazole-based molecules via van leusen oxazole synthesis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7180750/
https://www.ncbi.nlm.nih.gov/pubmed/32244317
http://dx.doi.org/10.3390/molecules25071594
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