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Vanillin: A Promising Biosourced Building Block for the Preparation of Various Heterocycles

The preparation of heterocyclic compounds often involves the use of petroleum-based or non-renewable sources. Considering the actual societal and environmental awareness towards sustainable chemistry, new and green sources of organic carbon are sought. In this regard, vanillin is a molecular buildin...

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Autor principal: Gendron, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9300922/
https://www.ncbi.nlm.nih.gov/pubmed/35873060
http://dx.doi.org/10.3389/fchem.2022.949355
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author Gendron, David
author_facet Gendron, David
author_sort Gendron, David
collection PubMed
description The preparation of heterocyclic compounds often involves the use of petroleum-based or non-renewable sources. Considering the actual societal and environmental awareness towards sustainable chemistry, new and green sources of organic carbon are sought. In this regard, vanillin is a molecular building block that can be obtained from the depolymerization of lignin. Due to its different functional groups (hydroxyl, aldehyde, and methoxy) vanillin can undergo a variety of reactions leading to various heterocycles such as pyrimidines, quinoxalines, imidazoles or thiazoles to name a few. This mini-review will focus on the preparation of accessible heterocycles building blocks from the vanillin moiety in regard to the medicinal, pharmaceutical, and material fields.
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spelling pubmed-93009222022-07-22 Vanillin: A Promising Biosourced Building Block for the Preparation of Various Heterocycles Gendron, David Front Chem Chemistry The preparation of heterocyclic compounds often involves the use of petroleum-based or non-renewable sources. Considering the actual societal and environmental awareness towards sustainable chemistry, new and green sources of organic carbon are sought. In this regard, vanillin is a molecular building block that can be obtained from the depolymerization of lignin. Due to its different functional groups (hydroxyl, aldehyde, and methoxy) vanillin can undergo a variety of reactions leading to various heterocycles such as pyrimidines, quinoxalines, imidazoles or thiazoles to name a few. This mini-review will focus on the preparation of accessible heterocycles building blocks from the vanillin moiety in regard to the medicinal, pharmaceutical, and material fields. Frontiers Media S.A. 2022-07-07 /pmc/articles/PMC9300922/ /pubmed/35873060 http://dx.doi.org/10.3389/fchem.2022.949355 Text en Copyright © 2022 Gendron. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Chemistry
Gendron, David
Vanillin: A Promising Biosourced Building Block for the Preparation of Various Heterocycles
title Vanillin: A Promising Biosourced Building Block for the Preparation of Various Heterocycles
title_full Vanillin: A Promising Biosourced Building Block for the Preparation of Various Heterocycles
title_fullStr Vanillin: A Promising Biosourced Building Block for the Preparation of Various Heterocycles
title_full_unstemmed Vanillin: A Promising Biosourced Building Block for the Preparation of Various Heterocycles
title_short Vanillin: A Promising Biosourced Building Block for the Preparation of Various Heterocycles
title_sort vanillin: a promising biosourced building block for the preparation of various heterocycles
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9300922/
https://www.ncbi.nlm.nih.gov/pubmed/35873060
http://dx.doi.org/10.3389/fchem.2022.949355
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